Magnetohydrodynamic flow past a circular cylinder

This paper deals with the slow-flow problem of an incompressible, viscous, electrically conducting fluid past a circular cylinder in an aligned magnetic field. The solutions for the velocity and magnetic fields are sought by the method of matched asymptotic expansions under the assumptions:R, R _mM1, such thatR=O(R _m). The influence ofR andR _m on this solution is studied toO(R/(logM)²) andO(R/logM), respectively.

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Zusammenfassung Die Arbeit behandelt das Problem des langsamen Fliessens einer nicht zusammendrückbaren zähen elektrisch leitenden Flüssigkeit, die um einen Kreiszylinder mit parallel zur Strömung gerichtetem Magnetfeld strömt. Die Lösungen für die Geschwindigkeit und das Magnetfeld werden gefunden durch die Methode der angepassten asymptotischen Entwicklungen unter den VoraussetzungenR, R _mM1, so dassR=O(R _m). Der Einfluss vonR undR _m auf diese Lösungen wird fürO(R/(logM)²) bzw.O(R _m /logM) untersucht.

     

Kinetics of the displacement of aqua ligands from cis-diaqua(ethylenediamine)-platinum(II)perchlorate by adenosine 5′-monophosphate in aqueous medium

The kinetics of the interaction of adenosine 5-monophosphate (5-AMP) with cis-[Pt(en)(H₂O)₂]²⁺ have been studied spectrophotometrically as a function of [Pt(en)(H₂O)₂]²⁺, [5-AMP] and temperature at pH 4.0, where the substrate complex exists predominantly as the diaqua species. Both N1 and N7 donor sites of 5-AMP are active for coordination to Pt at this pH. Base stacking and metal-induced macrochelate formation of 5-AMP plays a vital role in determining the concentration limit of 5-AMP during kinetics. Substitution occurs in two consecutive steps; both dependent on the 5-AMP concentration. Activation parameters for both steps have been calculated. The low H ₁ (42.76 ± 1.64 kJ mol^–1) and large negative values of S ₁ (–112.1 ± 5.1 J K^–1 mol^–1) as well as H ₂ (58.1 ± 1.4 kJ mol^–1) and S ₂ (–84.2 ± 4.4 J K^–1 mol^–1) indicate associative modes of activation for both ligand substitution processes in the two consecutive steps.     

Direct synthesis of polyamides by N-acyl phosphoramidites

A variety of N-acyl phosphoramidites were prepared from chlorophosphites and amide derivatives, and their structures were determined with the aid of ¹H-, ¹³C-, and ³¹P-NMR, and IR spectroscopies. These phosphoramidites were employed in direct polycondensation reaction of dicarboxylic acids and diamines under various conditions resulting in polyamides with inherent viscosities of 0.1 to 1.13. The best results were obtained when aliphatic dicarboxylic acids and aromatic diamines were condensed by 2-(N-methylacetamido)-1,3,2-dioxaphospholane in nitriles.     

Gravimetric determination of molybdenum and its separation from other metals with n-benzoylphenylhydroxylamine

N-Benzoylphenylhydroxylamine is employed as a precipitant for the determination of molybdenum (VI). The precipitate can be weighed either directly or as molybdenum trioxide after ignition. Molybdenum can be determined in the presence of appreciable amounts of iron(III), cobalt(II), copper(II), chromium(VI) and vanadium (V).     

Reflection spectra and optical constants of quasicrystalline Al-Pd-Re films in the IR region

Optical properties of quasicrystalline Al-Pd-Re films have been investigated in the mid and far IR regions. Films were deposited on sapphire substrates using layer-by-layer ion-plasma sputtering with subsequent vacuum annealing. Reflection spectra have been measured in a wide IR spectral range from 50 to 7500 cm^?1. The complex dielectric function of the films was determined from the experimental data by dispersion analysis of the reflection spectra. The frequency dependence of the real part of the optical conductivity was calculated.     

Changes in Triterpenes in Alismatis rhizoma after Processing Based on Targeted Metabolomics Using UHPLC-QTOF-MS/MS

Alismatis rhizoma (AR) has been used as an herbal medicine in China for over a thousand years. Crude AR, salt-processed AR (SAR), and bran-processed AR (BAR) are recorded in the Pharmacopoeia of the People′s Republic of China. However, the differences of chemical composition between crude AR and its processing products remain limited. In this study, triterpenes were identified from crude AR, SAR, and BAR by ultra-high performance liquid chromatography coupled with quadrupole time-of-flight-mass spectrometer (UHPLC-QTOF-MS/MS). Subsequently, the differences of triterpenes between the crude AR and processed ARs were compared via a targeted metabolomics approach. Finally, a total of 114 triterpenes were identified, of which 83, 100, and 103 triterpenes were found in crude AR, SAR, and BAR, respectively. After salt-processing, there were 17 triterpenes newly generated, 7 triterpenes with trends of increasing, and 37 triterpenes decreased. Meanwhile, 56 triterpenes including 21 newly generated and 35 with significant increases were observed in BAR. This study could be benefit to investigate the processing mechanism of AR, as well as support their clinical applications.