A Kerr effect study of microwave behaviour of partially magnetised ferrites

Magneto-microwave Kerr effect has been experimentally studied on three ferrite samples in the Polder-Smit loss region. Experimental data have been compared with the theoretical values which were calculated on the basis that the real part of the permeability tensor element μ′ is given by Green and Sandy's expressions (IEEE Trans. Microwave Theory Tech. MTT-22, 641 (1974)). This has a term given by Schlomann for μ′₀, the permeability for the demagnetised state. No agreement is found between theoretical and experimental values hence the above expression for ν′₀ has been substituted by another one given by Sandy (Raytheon Tech. Memor. T-815 (1969)) which involves the average demagnetisation factor N. It is found that there is a good agreement between the theory and the experiment provided N is assumed to depend linearly on the magnetisation of the sample.     

Fourier transform 13C NMR analysis of benzodiazepines

The natural abundance carbon-13 nuclear magnetic resonance spectra of diazepam, clonazepam, flurazepam and chlordiazepoxide were recorded in suitable solvent using the Fourier transform technique on a JEOL FX-60 spectrometer. The relaxation time (T₁) of these compounds were also measured. The chemical shift of the various carbon resonances have been assigned on the basis of chemical shift theory, multiplicity generated in single-frequency off-resonance decoupled spectra, relaxation time and the chemical shifts of the model compounds.     

Anomalous permeability in Polder-Smit region of ferrites

A study of the magneto-microwave Kerr effect on two samples of ferrites lying in the Polder-Smit region gives a negative value of μ', the real part of the transverse diagonal term of permeability tensor. There is a negative peak for μ' at a d.c. magnetization approximately equal to $\text{3}\text{4}$ of the saturation magnetization.     

Michael Addition Reaction of Thioacetic Acid (AcSH) to Conjugated Alkenes Under Solvent- and Catalyst-Free Conditions

A new and convenient procedure has been developed for the Michael addition reaction of thioacetic acid (AcSH) to a variety of conjugated alkenes under solvent- and catalyst-free conditions. These reactions proceeded in 5–60 min and produced the desired products in good to high yields.     

Synthesis,Physicochemical and Optical Characterization of Novel Fluorescing Complex: <Emphasis Type="Italic">o</Emphasis>-Phenylenediamine—Benzoin

The complex of o-phenylenediamine (o-PDA) and benzoin (BN) was synthesized adopting solid state reaction by mixing of their melt together followed by chilling. The phase diagram study shows the formation of a complex in 1:1 molar ratio with congruent melting point and two eutectics lying on either side of complex. The formation of complex was confirmed using the FTIR, NMR, mass spectroscopy, powder XRD and DSC studies. The optical properties of the parent component, their complex and few other compositions nearby the complex were studied using absorption and laser luminescence techniques. The significantly higher green/yellow emission was noted with newly synthesized complex as compared to that of their parents as well as other compositions of o- PDA and BN.     

Effect of fuel content on formation of zinc aluminate nano and micro-particles synthesised by high rate sol–gel autoignition of glycine-nitrates

The autoignition technique using glycine as fuel and related nitrate salts as an oxidiser is able to produce zinc aluminate spinel. The precursors were synthesised with lean and rich fuel at pH of 7.0 and the materials so obtained were calcined at various temperatures ranging from 600–1200°C. The autoignition process of precursors was studied by the simultaneous thermo-gravimetric and differential thermal analyses to determine the ignition mechanism. The calcined powders were characterised by X-ray diffraction, Brunauer–Emmett–Teller technique and transmission electron microscopy. The product contains nano-sized particles with an average size of approximately 20 nm. The XRD patterns showed the formation of ZnO in the powder obtained by the fuel-rich precursor and calcined at 600 C which disappears at 800 C due to solid-state reaction and proper crystallisation after heat treatment. The results presented here can be useful in manufacturing nano and micro-sized ZnAl₂O₄ on an industrial scale using the combustion technique.     

1H NMR‐based metabolomics exploring urinary biomarkers correlated with proteinuria in focal segmental glomerulosclerosis: a pilot study

Focal segmental glomerulosclerosis (FSGS) is a common glomerulonephritis, and its rates of occurrence are increasing worldwide. Proteinuria is a clinical defining feature of FSGS which correlates with the severity of podocyte injury in patients with nephrotic‐range protein excretion. Metabolite biomarkers corresponding with the level of proteinuria could be considered as non‐invasive complementary prognostic factors to proteinuria. The urine samples of 15 patients (n = 6 women and n = 9 men) with biopsy‐proven FSGS were collected and subjected to nuclear magnetic resonance (NMR) analysis for metabolite profiling. Multivariate statistical analyses, including principal component analysis and orthogonal projection to latent structure discriminant analysis, were applied to construct a predictive model based on patients with proteinuria >3000 mg/day and <3000 mg/day. In addition, random forest was performed to predict differential metabolites, and pathway analysis was performed to find the defective pathways responsible for proteinuria. Ten metabolites, significant in both statistical methods (orthogonal projection to latent structure discriminant analysis and random forest), were considered as prognostic biomarkers for FSGS: citrulline, dimethylamine, proline, acetoacetate, alpha‐ketoisovaleric acid, valine, isobutyrate, D‐Palmitylcarnitine, histidine, and N‐methylnicotinamide. Pathway analysis revealed impairment of the branched‐chain amino acid degradation pathways in patients with massive proteinuria. This study shows that metabolomics can reveal the molecular changes corresponding with disease progression in patients with FSGS and provide a new insight for pathogenic pathways. Copyright © 2016 John Wiley & Sons, Ltd.     

1-(1-aryl-3-ethylthiocarbamido)-4-arylaminothiocarbonyl)- piperazines as possible anticonvulsants

Several 1-(1-aryl-3-ethylthiocarbamido)-4-(arylaminothiocarbonyl)piperazines were synthesized as possible anticonvulsants. These 1,4-disubstituted piperazines were characterized by their sharp melting points and elemental and spectral analyses.     

Adhesion and interfacial interactions of BaO–SiO<Subscript>2</Subscript>–B<Subscript>2</Subscript>O<Subscript>3</Subscript>-based glass-ceramic seals and AISI430 interconnect for solid oxide fuel cell applications

In the present work, adhesion, leak rate, and chemical compatibility of a series of borosilicate-based glasses, belonging to the ternary BaO–SiO₂–B₂O₃ system, with AISI 430 alloys as interconnect were investigated for solid oxide fuel cell applications. Wetting angle and deformation behavior of the selected glasses with temperature and time were initially characterized with the hot-stage microscope. It was observed that the temperature ranges of wetting for all combinations were greater than 1000 °C. Significant deformation did not appear in the samples over soaking time at sealing temperature. In the next step, the leakage tests of AISI430/glass-ceramic couples were performed. The sample containing 32 % molar BaO (Ba32) had no gas leakage; a low leak rate of 10^?7to 10^?8 Pam³ s^?1 was obtained for the glass with 37 % molar BaO (Ba37) and big leak of the system (10^?3to 10^?4 Pam³ s^?1) for Ba42. Possible interfacial reactions between the as-received glass and cell ingredients and aging up to 100 h were studied by scanning electron microscopy in conjunction with energy-dispersive X-ray spectroscopy and X-ray dot mapping. The results showed that the Ba32 and Ba37 glasses coupled with AISI had fine adhesion, which remained stable under these conditions and were compatible with the interconnect. So, the use of these glass-ceramics will probably be successful in joining the ceramic electrolytes to the metallic interconnect.     

Extraction of Cu(II) with Acorga M5640 using hollow fibre liquid membrane

The extraction of copper from sulphuric/sulphate solutions using a hollow fibre module as contactor was studied. The aldoxime Acorga M5640 was used as an extractant. The effects on the extraction rate of the flow-rates, the concentrations of copper and extractant, pH, and the presence of Na₂SO₄ in the feed phase were investigated. The overall mass transfer coefficient for copper extraction was calculated from the experimental data and was compared with the value evaluated by the resistance in the series model. The extraction process was found to be governed by the diffusion in the boundary aqueous layer and also by the chemical reaction. The kinetic data obtained were used to simulate the extraction of copper with the pseudo-emulsion-based hollow fibre with strip dispersion technique. The accordance between the results thus calculated and the experimental data was found to be satisfactory, particularly for dilute feed solutions.