Investigation of turbulent flow field in a Kenics static mixer by Laser Doppler Anemometry

The main purpose of the present paper was to apply the Laser Doppler Anemometry (LDA) technique to measure turbulent liquid flow in a Kenics static mixer. The LDA set-up was a one-channel backscatter system with argon-ion laser. Measurements in the static mixer were carried out for three values of the Reynolds number: 5000, 10000, and 18000. Water was used as the process liquid. Values of the axial and tangential components of the local, mean, and root mean square velocities were measured inside the static mixer. It was observed that the shape of the velocity profile depends strongly on the Reynolds number, Re, as well as on the axial, h, and radial, α, position of the measurement point. Strong dependence of the velocity fluctuations on the Reynolds number was found in the investigated range of Re and the measurement point position. Furthermore, one-dimensional energy spectra of the velocity fluctuations were also obtained by means of the Fast Fourier Transform. Fluctuation spectra of the axial and tangential velocities provided information about the energy density of velocity fluctuations in the observed range of Reynolds numbers. A study of the energy spectra led to the conclusion that the energy density increases with the increasing radial distance from the mixer walls at constant values of h, _Re, and α. Minor variations in the mean value of the energy density, E, were observed together with variations of the measurement point angular position, α. In addition, it was observed that an increase of the Reynolds number causes significant increase of the power spectral density.     

Retention behavior of peptides in hydrophilic-interaction chromatography

Selected hydrophilic interaction chromatography (HILIC) columns packed with bare silica, bridge-ethyl hybrid silica, or an amide sorbent chemistry were utilized for an investigation of chromatographic behavior and separation selectivity of tryptic peptides. Retention model was proposed allowing for retention prediction of peptides with correlation coefficient R(2)~0.92-0.97 for various columns. The values of optimized amino acid retention coefficients were compared to those obtained for reversed-phase liquid chromatography (Gilar et al., Anal. Chem. 2010, 82, 265-275) and used to elucidate the impact of different amino acid on peptide HILIC retention. In contrast to reversed-phase chromatography, where presence of Phe, Trp, Ile, and Leu amino acid residues in sequence strongly promoted, and presence of hydrophilic His, Lys and Arg residues strongly reduced peptide retention, the effects of these amino acid residues in HILIC were opposite (His, Lys and Arg promote, Phe, Trp, Ile and Leu demote peptide retention in HILIC). Retention coefficient optimized for pH experiments illustrated the impact of silanols on HILIC retention.     

Rapid measurement of sphingolipids from Arabidopsis thaliana by reversed-phase high-performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry

Changes in sphingolipids have been associated with profound effects in cell fate and development in both plants and animals. Sphingolipids as a group consist of a large number of different compound classes of which numerous individual species may vary in response to environmental stimuli to affect cellular responses. The ability to measure all sphingolipids simultaneously is, therefore, essential to an understanding of the biochemical regulation of sphingolipid metabolism and signaling molecules derived from it. In the model plant Arabidopsis thaliana, the major sphingolipid classes are glycosylinositolphosphoceramides, glucosylceramides, hydroxyceramides and ceramides. Other minor but potentially important sphingolipids are free long-chain bases and their phosphorylated derivates. By using a single solvent system with reversed-phase high-performance liquid chromatography coupled to electrospray ionization tandem mass spectrometry detection we have been able to separate and measure 168 sphingolipids from a crude sample. This greatly speeds up and simplifies the analysis of plant sphingolipids and should pave the way for a better understanding of their role in plant performance.     

On the Milnor K-theory of the function fields of quasihomogeneous cones

Let V be a quasihomogeneous normal variety. The aim of this paper is to describe the Milnor K-theory of the function field of V in terms of the second residue homomorphisms associated with subvarieties and resolution data of V.Supported by KBN, 2 P301 010 06.     

Nonequilibrium solvent polarization in kinetics of SN2 reactions

The solvent effect on the experimental activation barriers for the reactions of methyl iodide with chloride and thiocyanate ions was analyzed according to the Marcus and Shaik theories, considering S_N2 mechanism in terms of a single electron shift. The linear increase in the solvent reorganization energy of the Marcus theory (after removing contributions from the specific solvation) with the solvent Pekar factor, describing the effect of the nonequilibrium solvent polarization, was observed for six aprotic solvents. The direct support of the title effect based on the Shaik theory was less evident; however, in general, the calculated activation barriers in 10 solvents change parallel with the experimental ones. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 35: 61–66, 2003     

On the connectivity of graphs generated by a sum of random mappings

We consider four models of random directed multigraphs with n labeled vertices of out-degree d. First we establish formal relationships between our models with respect to exact and asymptotic (as n → ∞) probabilities of possessing a graph monotone property. We also study the asymptotic behavior of the strength of connectivity of the underlying simple graphs when d = o(n). © 1993 John Wiley & Sons, Inc.     

Calculations of 1H NMR coupling constants for conformational studies of isomeric pentofuranosyl nucleosides

The SCF FPT method in the INDO approximation of molecular orbital theory is employed for calculations of ¹H NMR cisoidal coupling constants in model compounds. Obtained results are used for finding conformational states of α-xylo-, β-lyxo-, and α-2′-deoxyribonucleosides in solution.     

Two parameter donor-acceptor approach to solvent effects on the electrode kinetics of cations

A two parameter approach to solvent variations in the electroreduction rate constants of cobalt complexes and europium cations is presented and discussed in terms of solvent—solute and solvent—solvent interactions.

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Ein Zwei-Parameter Donor-Acceptor-Ansatz für Lösungsmitteleffekte bei der Elektrodenkinetik von Kationen (Kurze Mitteilung)

Zusammenfassung Es wird eine Zwei-Parameter-Annäherung der Lösungsmitteleinflüsse auf die Geschwindigkeitskonstanten der Elektroreduktion von Kobalt-Komplexen und Europium-Kationen präsentiert und auf der Basis von Lösungsmittel—gelöster Stoff- und Lösungsmittel—Lösungsmittel-Wechselwirkung diskutiert.

     

THE PHOTOTOXICITY OF 2,5-DIPHENYLOXAZOLE (POP) AND 1,4-BIS(5-PHENYLOXAZOL-2-YL)BENZENE (POPOP)

Abstract 2,5-Diphenyloxazole (POP) is widely used for the determination of radioactivity by scintillation counting. It has been found to be phototoxic to the yeasts Saccharomyces cerevisiae and Candida utilis , to the first instar larvae of the mosquito Aedes aegypti , to the crustaceans Daphnia magna and Artemia salida , as well as to the eggs of Drosophila melanogaster . The related molecule 1,4-bis(5-phenyloxazol-2-yl)benzene (POPOP) is also phototoxic, but to a lesser degree. Both POP and POPOP can sensitize the formation of singlet oxygen.