Preparation of some nickel(II) and copper(II) complexes of the SCHIFF-Base derived from Acetophenone and Ethylenediamine

Preparation and properties of the following Ni^II and Cu^II complexes of the Schiff base derived from acetophenone and ethylenediamine (BAPE) and also of the mixed Ni^II and Cu^II chelates with BAPE and acetylacetone (acac-H) are described: In each case the Schiff base, BAPE, acts as a neutral bidentate ligand. The complexes are characterised by electronic spectra, magnetic susceptibilities, conductivities and elemental analyses. Pseudotetrahedral structure is proposed for M(BAPE)C1₂, while tetragonal structure for [M(BAPE)(acac)(H₂O)₂]C_lO₄ (M = Ni and Cu). The complex [Ni(BAPE) (acac)]ClO₄ has been found to be square planar.     

Titration curves of p-aminobenzoic acid–formaldehyde polymer in relation to its structure

p-Aminobenzoic acid and formaldehyde were condensed in the presence of acid catalyst. The linear condensation polymer thus obtained was then separated into four fractions by a fractional precipitation method. Conductometric titrations were carried out on these four polymer fractions and the conglomerate in nonaqueous solvents with acid as well as base. The titration curves indicated a large number of additional breaks before the complete neutralization of COOH or NH₂ groups. These observations have been interpreted in terms of degree of polymerization and the structure of the polymer.     

Electrophoretic and viscometric studies of the interactions of polymethacrylamide and polyacrylamide with electrolytes in aqueous solutions

Free electrophoresis and viscometry were used to study the effects of salts (perchlorates, thiocyanates, chlorides and sulphates of uni- and bivalent metals) on the properties of polyacrylamide and polymethacrylamide in aqueous solutions. In salt solutions, in the electric field both polymers behave as polyanions. It may be inferred from electrophoretic measurements that both anions and cations are bound on the polymer chain; the degree of binding depends on the nature of the ions. The viscometric data show that there is a pronounced salting-in effect of cations (increasing with increasing surface charge density); the effect of anions is either secondary (for polyacrylamide) or rather unfavourable to dissolution (for polymethacrylamide).     

Anwendung der Massenspektrometrie zur Strukturaufklärung von Alkaloiden. 4. Mitt.: Zur Struktur des Rhazidins

Rhazidin kann durch LiAlH₄-Reduktion in Quebrachamin übergeführt werden. Für den basischen Bestandteil des Alkaloides ergibt sich daher Formel V. Umgekehrt ist die Verbindung V durch Oxydation von Quebrachamin mit Peressigsäure in guter Ausbeute zugänglich.

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Use of ultrasonics in shear layer cavitation control

In this paper we report results from some investigations on the use of ultrasonics in controlling hydrodynamic cavitation in the shear layer downstream of a sudden expansion. Control of this type of cavitation has been achieved by modulating the local pressure that was experienced by a nucleus present in the shear layer. This modulation was made possible by using a piezoelectric device, termed as Ultrasonic Pressure Modulator (UPM). The performance of UPM has been studied at different dissolved gas concentrations with electrolysis bubbles as nuclei. Control of cavitation due to natural nuclei has also been attempted. Efficiency of UPM, in reducing cavitation, was seen to be dependent on the driving frequency employed. Experimental and numerical studies have been conducted to bring out the physics behind this approach of cavitation control. Different measures of cavitation control have been identified and some possible applications of this method have also been outlined.     

Transfer Thermodynamics of Protein in Denaturing and Stabilizing Media

Free energies of transfer (ΔG_t) of RibonucleaseA (RNaseA) from water to aqueous solutions of urea (4 M, 6 M and 8 M), a protein denaturing solvent as well as ΔG_t of RibonucleaseA, β‐Lactoglobulin, α‐Chymotripsin and ChymotrypsinogenA from water to aqueous glycerol (10%, 20%, 30% and 40%), a protein stabilizing solvent has been dissected into cavity term [ΔG_t(cav)] and interaction term [ΔG_t(int)]. The interaction free energy includes all types of interactions like hard‐soft, hydrogen bonding, electrostatic, etc. The cavity forming free energies have been calculated using the standard version of scaled particle theory (SPT) with well‐reported SPT parameters. It has been found that transfer free energies of cavity terms ΔG_t(cav) for native protein from water to urea‐water and water to aqueous glycerol follow almost opposite trends. This primarily indicates there may be some correlation between cavity creation energies and protein denaturing and stabilizing ability of a solvent. The results are in agreement with those obtained from preferential binding coefficient studies in these media.     

A simple mathematical model for seasonal planktonic blooms

We show how the inclusion of the defense strategy by different species can alter the prediction of simple models. One of the defense strategy by the phytoplankton population against their grazer is the release of toxic chemicals. In turn the zooplankton population reduces there predation rate over toxin producing phytoplankton (TPP) to protect themselves from those toxic chemicals. Thus, when the level of toxicity is high, the grazing pressure is low and when the level of toxicity is low or when the toxin is absent, the grazing pressure is high. Here we have considered a TPP–zooplankton system where the rate of toxin liberation and the predation rate vary with zooplankton abundance. We observe that our proposed model has the potential to show different dynamical behaviour that are similar to that seen in real‐world situations. Further, we consider three different functional forms for the distribution of the toxins and compare them using latin hypercube sampling technique and found that the functional forms seem to have no effect in determining the final outcome of the system. Copyright © 2009 John Wiley & Sons, Ltd.