Conductivity and viscosity studies of ethylene carbonate based solutions containing lithium perchlorate

Specific conductivities and viscosities of lithium perchlorate at four different concentrations (0.5, 1.0, 1.5 and 2.0 M) in ethylene carbonate (EC) based binary mixed solvent systems at 25°C are reported. The co-solvents chosen were tetrahydrofuran (THF), 1,2-dimethoxyethane (DME) and 1,3-dioxolane (DOL). Viscosity variations in all the three mixed solvent systems without electrolyte showed negative deviation from ideal behaviour thereby indicating the occurrence of a structure breaking effect in these three different binary systems. The increase in viscosity with increase in concentration of LiClO₄ is attributed to the structural enhancement through the formation of a solvated complex which occupies interstitials in the solvent mixtures. 1 M LiClO₄ solution shows maximum specific conductivity at 30 vol % EC for EC + DME and EC + DOL mixtures and at 50 vol % EC for EC + THF mixtures. Conductivity variations are explained on the basis of preferential solvation of lithium perchlorate by co-solvents (THF, DME and DOL) in their respective mixtures with ethylene carbonate.     

Simulation of molecular weight distribution and cyclic oligomer formation in the polymerization of nylon 6

The reversible polymerization of nylon 6 including ring opening, polycondensation, polyaddition, and cyclization reactions as well as the reaction with monofunctional acids was simulated for an isothermal batch reactor at 235°C. The cyclic oligomer concentrations, the molecular weight distributions, and its moments have been computed using a chain length-dependent equilibrium constant for the cyclization reaction. Even though the cyclization step does not influence the monomer conversion considerably, it does effect the molecular weight distribution and its moments.     

Prediction of surface tension of athabasca bitumen

Athabasca bitumen was characterized by dividing it into sixteen pseudo components. Using mean boiling point, molecular weight and specific gravity data, the critical properties of the pseudo components were estimated from available correlations. Two approaches for the prediction of bitumen surface tension were investigated. It was found that the surface tensions predicted by the principle of corresponding states and the Rice-Teja correlations were in general agreement with the published experimental data. In addition, these models successfully predicted the effect of temperature on surface tension at temperatures greater than about 60°C.     

Solution of mass transfer in step growth polymerization in films with bulk in equilibrium

We have analyzed step growth polymerization in a flat film with finite mass transfer resistance. We have shown rigorously that the molecular weight distribution (MWD) at equilibrium is given by the Flory distribution, and under reaction the form of the MWD does not change if the feed is either pure monomer or in equilibrium initially. Extensive computations have shown that it is possible to split the film into growing interfacial and shrinking bulk regions. It is possible to obtain similarity transformations of concentrations of condensation product, and polymer as time invariant profiles. Based on this finding, we have determined a solution for step growth polymerization with finite mass transfer in films. The results lie within 5% of the “exact” numerical computations, for all possible variations of parameters.     

Gas hold-up in non-newtonian solutions in a bubble column with internals

Bubble characteristics and gas hold-up were studied in a two phase (air-aqueous CMC solution) bubble column provided with helical coils and straight tubes as internals. The effects of superficial gas velocity, rheological properties, and volume fraction covered by the internals, on gas hold-up were studied. Hold-up values determined directly and by simultaneous pressure drop measurements matched well. Enhancement of gas hold-up values up to 55 per cent was achieved in systems using internals. The gas hold-up results were also compared with the values obtained from correlations reported in the literature.     

A simple correlation for estimating viscosities of solutions of salts in aqueous,non-aqueous and mixed solvents applicable to high concentration,temperature and pressure

A new correlation is proposed to correlate the viscosities of salt solutions in aqueous, non-aqueous solvents and their mixtures. The correlation involves two parameters i.e. solvation number and ion-solvent interaction coefficient, which are well-documented quantities in the literature. The proposed correlation has been examined on the experimental viscosity data of salt solutions in aqueous, non-aqueous and their mixtures up to 473 K and 31 MPa pressure. The salts with various ionic charges were employed for testing the proposed correlation. Several non-aqueous solvents like dimethyl sulphoxide, alcohols and formamide were included for the data regression. The viscosities of these solutions can be correlated to within 0.7%.     

Thermodynamic and Kinetic Effects of Oxygen Removal on the Thermal Conductivity of Aluminum Nitride

High thermal conductivity, low dielectric constant, high electrical resistivity, low density, and a thermal expansion coefficient that matches well with that of silicon are the principal attributes of AIN that have attracted much attention over the past decade. It is also now well established that oxygen as an impurity lowers the thermal conductivity of AIN. Processing techniques have been developed which not only facilitate pressureless densification of AIN but also enhance its thermal conductivity. The present work explores the thermodynamics and the kinetics of oxygen removal and the resultant enhancement of thermal conductivity. Polycrystalline AIN ceramics were fabricated with Y₂O₃, Dy₂O₃, Yb₂O₃, CaO, BaO, or MgO as additives. Samples were sinter/annealed at 1850°C for up to 1000 min. The AIN grain size of sintered samples ranged between 2 and 9 μm. The samples typically contained two or three phases with the predominant phase being AIN. Secondary phases in Y₂O₃-doped AIN consisted of yttrium aluminates which were along three grain junctions and along grain facets. The presence of Y₃Al₅O₁₂, YAIO₃, and Y₄Al₂O₉, as well as Y₂O₃, depending upon the Y₂O₃/Al₂O₃ ratio, was revealed by X-ray diffraction. Thermal conductivity increased with the amount of additive and annealing time. Thermal conductivity also depended on the type of additive. Samples with thermal conductivity up to 200 W/(m · K) were fabricated. The variation in thermal conductivity with the type and the amount of the additive is explained on the basis of the thermodynamics of oxygen removal. In particular, the higher thermal conductivity of CaO-doped, in comparison with MgO-doped, samples is rationalized on the basis that the free energy of formation, ΔG°, of CaAl₂O₄ is less than that of MgAl₂O₄. It is proposed that the higher the |ΔG°|, with ΔG° < 0, the higher is the resultant thermal conductivity. An increase in the thermal conductivity with annealing time is attributed to the kinetics of oxygen removal from AIN grains.     

Viscosity of compressed cold lake bitumen

Viscosity data over a temperature range of 37-115°C and a pressure range of 0-10 MPa gauge are presented for a Cold Lake bitumen sample. These data show that the compression of Cold Lake bitumen results in a significant increase in its viscosity. Results are compared with those from a similar study on an Athabasca bitumen sample. Also presented are two correlations for the effects of pressure and temperature on the viscosity of Cold Lake bitumen.