Pulsatile flow between permeable beds

Pulsatile flow of a viscous fluid between two permeable beds is analyzed. The flow between and through the permeable beds are governed by the Navier-Stokes equations and Darcy's law, respectively. The velocity field and the volume flux are obtained for several cases and discussed. Further, when the permeability parameter k→0, the results agree with those of Wang (J. Appl. Mech. 38 (1971) 553).     

High spin properties of 124Ba

The ¹²⁴Ba nucleus is investigated on the basis of the method of statistical mechanics by assuming the nucleons to move in triaxially deformed Nilsson potential. The variation in the Fermi energies of protons and neutrons is studied as a function of spin and temperature. The Fermi energies determined as a function of angular momentum is used to study the dependence of shell correction on angular momentum using the Strutinsky smoothing procedure. The most important observation is that the shell correction is almost the same for all spins for ¹²⁴Ba. The spin cutoff parameter and the single particle level density parameter are studied as a function of spin and temperature. Constant entropy lines drawn by plotting the excitation energy against angular momentum are found to be roughly at constant energy above the yrast line and are almost equally spaced. It is observed that no yrast traps are present for ¹²⁴Ba.     

Ultrasound-assisted analyte extraction for the determination of sulfate and elemental sulfur in zinc sulfide by different liquid chromatography techniques

The speciation and determination of sulfate (SO4(2-)) and elemental sulfur (S degree) in zinc sulfide (ZnS) using ion-chromatography (IC) and reversed-phase liquid chromatography (RPLC) respectively is described. Three sample pretreatment approaches were employed with the aim of determining sulfate: (i) conventional water extraction of the analyte; (ii) solid-liquid aqueous extraction with an ultrasonic probe; and (iii) elimination of the zinc sulfide matrix via ion-exchange dissolution (IED). The separation of sulfate was carried out by an anion-exchange column (IonPac AS17), followed by suppressed conductivity detection. Elemental sulfur was extracted ultrasonically from the acid treated sample solution into chloroform and separated on a reversed phase HPLC column equipped with a diode array detector (DAD) at 264 nm. The achievable solid detection limits for sulfate and sulfur were 35 and 10 microg g(-1) respectively.     

Construction of anion‐responsive crosslinked polypseudorotaxane based on molecular recognition of pillar[5]arene

A pillar[5]arene pendant polymer (Poly‐P[5]A) is synthesized via ROMP using Grubb's first‐generation catalyst. GPC analysis of the polymer suggested ~30 pendant pillar[5]arene units in the polymer. Supramolecular polypseudorotaxane assembly is constructed by intermolecularly crosslinking pendant pillar[5]arene units using a bispyridinium guest via host–guest complexation. Formation of the polypseudorotaxane assembly is characterized by 1D/2D NMR techniques and DLS analysis. Moreover, anion‐responsiveness of the polypseudorotaxane assembly is demonstrated by ¹H NMR spectroscopic analysis using chloride anion as external stimulus. Scanning electron microscopic analysis of the poly‐P[5]A showed breath‐figure assembly and upon crosslinking with G.2PF₆ the polymer self‐assemble to give a supramolecular polymer network. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1508–1515     

Crystal and molecular structure of trans-bis(dodecylamine) bis(dimethylglyoximato)cobalt(III) nitrite

An octahedral geometry for the molecule of the title complex with very slight distortions around Co(III) is confirmed by single-crystal X-ray diffraction study. The molecular structure of the complex has been shown to contain two dodecylamine moieties in the trans orientations, two N-bonded dimethylglyoximato (DMG) groups and an uncoordinated nitrite ion.     

Detection of electrophoretically separated cytochromes P450 by element-labelled monoclonal antibodies via laser ablation inductively coupled plasma mass spectrometry

Numerous structurally and enzymatically similar cytochromes P450 (CYPs) are involved in the metabolism of xenobiotics and are present in different amounts and with different enzyme profiles in human tissues and cells. Analysis of their adaptively regulated and individually variable patterns is a peculiar analytical challenge. We developed a laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) based method for concomitant detection and semiquantitative determination of electrophoretically separated and blotted CYPs. The first results are given here for the two enzymes CYP1A1 and CYP2E1. Specific monoclonal antibodies directed against the enzymes were differentially labelled with europium via a covalently linked chelator and with iodine, respectively. Analysis of the modified antibodies shows that both europium and iodine are coupled to the heavy and the light chains of the antibodies. Also, the antibodies maintained their antigen-binding properties after labelling as demonstrated by LA-ICP-MS-analysed immunoblots. The method allowed us to detect specifically and concomitantly both CYP enzymes in complex biological samples, i.e. microsomes of rat liver and minipig duodenum, which are characterized by different levels and proportions of the two CYP enzymes. A strong CYP1A1 signal is found in liver microsomes of 3-methylcholanthrene-treated rats, while it is (nearly) absent in liver microsomes of rats treated with isonocotinic acid hydrazide (isoniazid). The constitutively expressed CYP2E1 is found in microsomes of both treatment groups. Duodenal microsomes of minipigs orally exposed to polycyclic aromatic hydrocarbons show a clear CYP1A1 signal. Low levels of CYP2E1 can also be detected in these microsomes. The LA-ICP-MS method allows concomitant determination of CYPs, thereby exhibiting sensitivity similar to that of conventional chemoluminescence detection via peroxidase-labelled secondary antibodies. The latter method allows readout of a single CYP protein in a 1D separation. Although the results presented here are only for labelling by use of the elements iodine and europium, the same strategy can be applied also for other lanthanide elements in combination with chelating compounds, so LA-ICP-MS of western blots offers a new capability to be applied for highly multiplexed CYP determinations via labelled antibodies.     

Robust stability analysis of stochastic neural networks with Markovian jumping parameters and probabilistic time‐varying delays

This article discusses the issue of robust stability analysis for a class of Markovian jumping stochastic neural networks (NNs) with probabilistic time‐varying delays. The jumping parameters are represented as a continuous‐time discrete‐state Markov chain. Using the stochastic stability theory, properties of Brownian motion, the information of probabilistic time‐varying delay, the generalized Ito's formula, and linear matrix inequality (LMI) technique, some novel sufficient conditions are obtained to guarantee the stochastical stability of the given NNs. In particular, the activation functions considered in this article are reasonably general in view of the fact that they may depend on Markovian jump parameters and they are more general than those usual Lipschitz conditions. The main features of this article are described in the following: first one is that, based on generalized Finsler lemma, some improved delay‐dependent stability criteria are established and the second one is that the nonlinear stochastic perturbation acting on the system satisfies a class of Lipschitz linear growth conditions. By resorting to the Lyapunov–Krasovskii stability theory and the stochastic analysis tools, sufficient stability conditions are established using an efficient LMI approach. Finally, two numerical examples and its simulations are given to demonstrate the usefulness and effectiveness of the proposed results. © 2014 Wiley Periodicals, Inc. Complexity 21: 59–72, 2016     

Thermodynamics and micellar properties of some surface active cobalt(III) metallosurfactants in nonaqueous medium

The critical micelle concentration (CMC) of four kinds of metallosurfactants of the type halogeno(dodecyl/cetylamine)‐bis(ethylenediamine)cobalt(III) has been studied in n‐alcohol and in formamide at different temperatures by electrical conductivity method. Specific conductivity data (at 293–313 K) served for the evaluation of temperature‐dependent CMC and the thermodynamic parameters such as standard Gibbs free energy changes (ΔG), enthalpies (ΔH), and entropies (ΔS) of micelle formation. CMCs have also been measured as a function of percentage concentration of alcohol added. It is suggested that alcohol addition leads to increase in formamide penetration into micellar interface that depends on the alcohol chain length. The results have been discussed in terms of increased hydrophobic effect (solvophobic interaction), dielectric constant of the medium, and the chain length of the alcohols, the surfactant in the solvent mixture. © 2006 Wiley Periodicals, Inc. Int J Chem Kinet 39: 22–31, 2007     

Transfer measurements for the Ti+Ni systems at near barrier energies

Large enhancements have been observed in the sub-barrier fusion cross sections for Ti+Ni systems in our previous studies. Coupled channel calculations incorporating couplings to 2⁺ and 3⁻ states failed to explain these enhancements completely. A possibilty of transfer channels contributing to the residual enhancements had been suggested. In order to investigate the role of relevant transfer channels, measurements of one- and two-nucleon transfer were carried out for ^46,48Ti+⁶¹Ni systems. The present paper gives the results of these studies.