Measurement of Gibbs energies of formation of CoF2 and MnF2 using a new composite dispersed solid electrolyte

Gibbs energies of formation of CoF₂ and MnF₂ have been measured in the temperature range from 700 to 1100 K using Al₂O₃-dispersed CaF₂ solid electrolyte and Ni+NiF₂ as the reference electrode. The dispersed solid electrolyte has higher conductivity than pure CaF₂ thus permitting accurate measurements at lower temperatures. However, to prevent reaction between Al₂O₃ in the solid electrolyte and NiF₂ (or CoF₂) at the electrode, the dispersed solid electrolyte was coated with pure CaF₂, thus creating a composite structure. The free energies of formation of CoF₂ and MnF₂ are (± 1700) J mol⁻¹; {fx37-1} The third law analysis gives the enthalpy of formation of solid CoF₂ as ΔH° (298·15 K) = −672·69 (± 0·1) kJ mol⁻¹, which compares with a value of −671·5 (± 4) kJ mol⁻¹ given in Janaf tables. For solid MnF₂, ΔH°(298·15 K) = − 854·97 (± 0·13) kJ mol⁻¹, which is significantly different from a value of −803·3 kJ mol⁻¹ given in the compilation by Barinet al.     

Epoxy/poly(methyl methacrylate) interpenetrating polymer networks—morphology,mechanical and thermal properties

Full and semi-IPNs were prepared from epoxy and poly methyl methacrylate (PMMA), by the sequential mode of synthesis and were characterized by measurements of ultimate tensile strength (UTS), elongation at break, modulus, and toughness. Aromatic polyamine adducts and ethylene glycol dimethacrylate were used as the crosslinkers for epoxy and comonomer/crosslinker for methyl methacrylate monomer, respectively. Higher UTS and modulus of the semi-IPNs over full IPNs were attributed to the higher probability of interpenetration. The weight retention in the thermal decomposition of the IPNs and semi-IPNs were higher than the epoxy homopolymer. This enhancement was presumably related to the presence of the unzipped methyl methacrylate monomer which acted as radical scavangers in the epoxy degradation. © 1994 John Wiley & Sons, Inc.     

Copper(II)‐Catalyzed Aerobic Oxidative Coupling between Chalcone and 2‐Aminopyridine via C?H Amination: An Expedient Synthesis of 3‐Aroylimidazo[1,2‐a]pyridines

A simple and efficient protocol has been developed for the synthesis of 3‐aroylimidazopyridines via copper(II) acetate‐catalyzed aerobic oxidative amination. A library of 3‐aroylimidazopyridines was synthesized from readily accessible chalcones and 2‐aminopyridines with high yields and regioselectivity. The reaction proceeds through a tandem Michael addition followed by an intramolecular oxidative amination. The successful application of this methodology for a gram‐scale reaction indicates its potential for bulk synthesis.

     

The effect of temperature on the surface tension and adsorption functions of the Fe-S-O melts – an analysis based on interaction parameters

The present investigation analyses the thermodynamic behaviour of the surfaces and adsorption as a function of temperature and composition in the Fe-S-O melts based on the Butler's equations. The calculated values of the surface tensions exhibit an elevation or depression depending on the type of the added solute at a concentration which coincides with that already present in the system. Generally, the desorption of the solutes as a function of temperature results in an initial increase followed by a decrease in the values of the surface tension. The observations are analyzed based on the surface interaction parameters which are derived in the present research.     

Quantification,characterization and fatty acid composition of lysophosphatidic acid in different rat tissues

The amount and composition of lysophosphatidate present in different rat tissues have been estimated by an internal standard method in which a synthetic unnatural isomer (1-heptadecanoyl-rac-glycerol-3-phosphate) was added to the total lipid extracts, and the fatty acid composition of purified lysophosphatidate was determined. Lipids from tissues were extracted under acidic conditions, and the lysophosphatidate was purified by solvent partitions followed by thin-layer chromatography in multiple solvent systems. The purified lipid was shown to be 1-acyl-sn-glycerol-3-phosphate by chromatographic and chemical analysis, by its resistance to hydrolysis when treated with phospholipase A₂ and also by its complete conversion to 1-acyl-sn-glycerol when treated with alkaline phosphatase. The fatty acid consituents of this lipid were determined by gas-liquid chromatography of the derived methyl esters. The concentrations (nmol/g of tissue) of lysophosphatidate in various tissues were: 86.2±4.2 in brain, 60.3±6.3 in liver, 46.4±6.5 in kidney, 30.6±5.0 in testis, 22.3 in heart and 19.3 in lung. Mostly (80%) saturated fatty acids were found to be present in this lyso lipid. A significantly high level of stearic acid was present in this lipid from all the tissues (50–60% in liver, kidney, brain and testis, and about 40% in heart and lung) compared to plamitic acid (10–15% in liver, kidney and brain and 25–30% in testis, heart and lung). The fatty acid compositions of phosphatidic acid, the putative product of lysophosphatidate acylation, from different tissues were also determined and palmitate was found to be the major saturated fatty acid. These results suggest that tissue lysophosphatidic acid is not only formed byde novo biosynthesis but is also generated via the breakdown of phospholipids such as phosphoinositides.     

Representation of thermodynamic properties of quaternary systems using interaction parameters

Integral excess free energy of a quaternary system has been expressed in terms of the MacLaurin infinite series. The series is subjected to appropriate boundary conditions and each of the derivatives correlated to the corresponding interaction coefficients. The derivation of the partial functions involves extensive summation of various infinite series pertaining to the first order and quaternary parameters to remove any truncational error. The thermodynamic consistency of the derived partials has been established based on the Gibbs-Duhem relations. The equations are used to interpret the thermodynamic properties of the Fe-Cr-Ni-N system.     

Applicability of butler’s equation in interpreting the thermodynamic behavior of surfaces and adsorption in Fe-S-O melts

Expressions for various second-order derivatives of surface tension with respect to composition at infinite dilution in terms of the interaction parameters of the surface and those of the bulk phases of dilute ternary melts have been presented. A method of deducing the parameters, which consists of repeated differentiation of Butler’s equations with subsequent application of the appropriate boundary conditions, has been developed. The present investigation calculates the surface tension and adsorption functions of the Fe-S-O melts at 1873 and 1923 K using the modified form of Butler’s equations and the derived values for the surface interaction parameters of the system. The calculated values are found to be in good agreement with those of the experimental data of the system. The present analysis indicates that the energetics of the surface phase are considerably different from those of the bulk phase. The present research investigates a critical compositional range beyond which the surface tension increases with temperature. The observed increase in adsorption of sulfur with consequent desorption of oxygen as a function of temperature above the critical compositional range has been ascribed to the increase of activity ratios of oxygen to sulfur in the surface relative to those in the bulk phase of the system.     

A Green Metal–Organic Framework-Cyclodextrin MOF: A Novel Multifunctional Material Based Triboelectric Nanogenerator for Highly Efficient Mechanical Energy Harvesting

The naturally available cyclodextrin has opened up a wide range of research avenues because of its superior characteristics such as being non-toxic, biocompatible, and edible. The cyclodextrin is the green multifunctional material that can add to the triboelectric series and extend its self-powered applications. The ultrasonic synthesized cyclodextrin metal–organic framework (CD-MOF) designed using sodium as a metal ion and cyclodextrin as a ligand for the triboelectric nanogenerator is reported. The various detailed characterizations of the CD-MOFs give an insight into the properties of the synthesized material. The Kelvin probe force microscopy suggests three types of CD-MOFs, exhibiting a positive potential. As per the surface potential, the output of the various CD-MOF based TENG is varied as alpha CD MOF/Teflon > gamma CD-MOF/Teflon > beta CD-MOF/Teflon. The alpha CD MOF/Teflon TENG produces an electrical output of 152 V, 1.2 μA, and 14.3 nC, respectively. The fabricated device output is utilized for powering numerous low-power electronics through a capacitor and bridge rectifier circuit. The multiunit Z-shaped TENG device is attached to various surfaces such as the shoe heel and the backside of the school bag, and the corresponding energy harvesting response is demonstrated.     

Phase Transformation Studies in U–xZr (x = 2, 5, 10 wt%) Alloys Using Dynamic Calorimetry

The thermo-kinetics aspects of phase transformations in U rich U–xZr binary alloys, with x = 2, 5 and 10 wt% Zr have been investigated using dynamic calorimetry. The on-heating and cooling transformations at controlled scan rates in the range, 1–99 K min^?1, have been monitored and the following transformation sequence is obtained at slow heating (3 K min^?1) of a U–2Zr alloy: (i) α or α′ (distorted orthorhombic martensite) + δ(UZr₂) → α + γ₂ (bcc phase enriched in Zr); (ii) α + γ₂ → β (tetragonal) + γ₂; (iii) β + γ₂ → β + γ₁ (bcc phase enriched in U); (iv) β + γ₁ → γ; (v) γ (bcc) → liquid (melting). Similar transformation sequence for other compositions with varying enthalpy effects has been witnessed for 5 and 10 Zr alloys. The observed transformation characteristics are rationalized for the effect of Zr content and heating/cooling rate variations.