Copper Complexes Obtained from the Schiff Base of Quinoline-2-Aldehyde and Aliphatic Diamines

Schiff base bis (2— quinolidene)- diamine gives a purple-red complex with copper ions with a λ_max at 530 mμ. The optimum pH for production of this complex is approximately 9.5. None of the metallic ions of the analytical groups II and III give rise to red complexes with the above Schiff base. Manganous (Mn²⁺) and stannous (Sn²⁺)ions as well as reducing agents such as hydrazine or hydroxylamine exert a catalytic effect on the rate of formation of these copper complexes. The thermal stability of the copper complex formed from the Schiff bases (2-quinoline-aldehyde with NH₂-(CH₂)_n-NH₂) is greater for diamine for which n = 4–6 than for n = 2–3.     

Non-markovian diffusion processes in polymers and a stretched exponential relaxation constitutive equation

Non-Markovian diffusion transport in polymers was studied. Applying the results of various researchers, a stretched exponential relaxation function was obtained and a linear viscoelastic constitutive equation formulated. Frequency dependent material functions, obtained from this constitutive equation were studied and the results successfully compared with experimental data for polyethylene oxide solutions. Sorption kinetics in a polymeric film were also studied. © 1994 John Wiley & Sons, Inc.     

Polyacrylic acid macromolecule—complexed zinc phosphate crystal conversion coatings

When water-soluble polyacrylic acid (PAA) macromolecules are introduced into zinc phosphating liquids, significant improvements in the yield of conventional zinc phosphate conversion films deposited on carbon steel surfaces are obtained. The improvements include controllability of crystal dimensions, degree of crystallinity, and coating weight. The conversion layer formed is a composite microstructure consisting of a bulk PAA polymer and complexed PAA continuously overlaying a uniform array of fine dense zinc phosphate crystals. Interfacial studies of the composite layer using infrared spectroscopy, energy-dispersive X-ray spectrometry associated with scanning electron microscopy, and X-ray photoelectron spectroscopy indicated that the functional carboxylic acid groups in the PAA molecules were strongly chemisorbed by the Zn atoms at the outermost surface sites of the crystal layers. The intermolecular bridging action of the surface Zn atoms which connect the PAA and the zinc phosphate crystal layers results in good adhesion at the PAA–crystal interfaces. In addition, the plasticized complex formation plays an essential role in increasing the stiffness and the ductility of the normally conventional crystal films. The flexibility of the complex coating surface and the thickness and surface roughness of the thin PAA overlayer all affect the adhesive force at the interface between the organic polymer topcoat and the complexed coating.     

Diels-alder adducts from safflower oil fatty acids: I. Maleic anhydride as dienophile

The Diels-Alder reaction between alkali conjugated and elaidinized safflower oil fatty acids and maleic anhydride was studied under various experimental conditions. The principal product which was obtained in 51–55% yields was a mixture of the adduct of maleic anhydride and maleic acid in 40∶60 proportions. The isolation and properties of this mixed adducts from the reaction mixture and their conversion to trimethyl, tributyl and triallyl esters are described. The trimethyl ester was also obtained in good yield from the methyl esters of the fatty acids and dimethyl maleate.     

Effect of casting conditions on the performance of porous cellulose acetate membranes in reverse osmosis

Several sets of porous cellulose acetate membranes were made using the same casting solution composition and gelation conditions but varying the casting solution temperature and solvent evaporation conditions. The films were tested in reverse osmosis experiments at 250 psig using aqueous feed solutions containing 3500 ppm NaCl. The results show that the product rate obtained at a given level of solute separation is independent of evaporation time in the range tested and, for a given casting solution composition, the temperature of the casting solution and conditions of solvent evaporation during film formation together constitute an important interconnected variable governing the porous structure of the resulting membranes. These results offer a new approach to the problem of developing more productive reverse osmosis membranes and have led to a new class of porous cellulose acetate membranes capable of giving product rates 100% to 150% higher than those of the best membranes reported, at any given level of solute separation under the experimental conditions used. These results are of practical importance in low-pressure reverse osmosis applications.     

Effect of boron nitride addition on some properties of aluminosilicate refractories

Conclusions An addition of 10–60 wt.% of boron nitride significantly alters the thermal conductivity, thermal expansion, and the elastic modulus of aluminosilicate refractories.As the boron nitride content is increased from 1–60% the strength of specimens heated in a nitrogen atmosphere with an oxygen content of 0.02% decreases.During cyclic heat treatment in an oxidizing atmosphere between 900 and 20°C additional bonds develop between the particles of the aluminosilicate and the oxygen-free additive. As a result the strength of the specimen increases.The thermal shock resistance of the specimens increases with an increase in the amount of boron nitride addition. Specimens with 40–50% boron nitride addition are in practice insensitive to temperature drops in the range 20–2400°C.Aluminosilicate refractories with the addition of 30–40 wt.% of boron nitride can be used as lining material in high temperature systems with brief nonsteady or cyclic work schedules.Translated from Ogneupory, No. 4, pp. 36–39, April, 1968.     

HYDRODYNAMIC MODELLING IN AN AIR-LIFT LOOP REACTOR

A simple hydrodynamic model is proposed for use in the design, scale-up and characterization of external loop air-lift reactors. The approach is based upon a momentum balance for the flow loop coupled with a drift-flux equation for the reactor riser and establishes a rational basis for a predictive model relating gas throughput to induced liquid flow and gas hold-up in a range of air-lift reactors. The effective resistance of the reactor, k, defined in terms of the total loss coefficients of the reactor and the aerated height of the two-phase riser, was identified to allow for the quantification of the influence of reactor design on the hydrodynamic variables. An extensive body of data for the air-water system, collected on two reactors with active volumes of 0·055 m³ and 0·3 m³, is presented and used, in conjunction with literature data encompassing a wide range of reactor geometries and flow conditions, to define a unique relationship between flow behaviour and reactor configuration. The model, which accounts for the prevailing flow regime in the reactor, provides a direct method of predicting hydrodynamic behaviour in relatively non-viscous systems.     

Liquid Immiscibility in the Systems X2O-MO-B2O3-SiO2 (X=Na, K; M=Mg, Ca, Ba) and Na2O-MgO-BaO-B2O3-SiO2

The limits of miscibility at 650°C were determined for compositions with the mole ratio SiO₂/B₂O₃=1.07 in the systems X₂O-MO-B₂O₃-SiO₂ (X = Na,K; M = Mg,Ca,Ba) and Na₂O-MgO-BaO-B₂O₃-SiO₂. The form of the miscibility gaps in the quaternary systems is similar to that previously described for the system Na₂O-ZnO-B₂O₃-SiO₂. The topography of miscibility gaps in systems of this type is discussed in detail. The extent of the miscibility gap is correlated with the polarizing power of each cation, X and M (Na > K and Zn ≅ Mg > Ca > Ba) both among the seven quaternary systems and within the single five-component system examined. The possibility of using empirical correlations observed among the quaternary systems to predict the behavior of other compositions, or of more complex systems, is explored.     

Solvent extraction of metals from chloride solutions

A review is presented of a series of investigations into the extraction of copper, iron, zinc and cadmium into kerosene solutions of Lix or Kelex reagents from aqueous solutions containing chloride ions. The effects of chloride ions on the extraction of copper and iron were smaller than might have been expected to result from the formation of inextractable metal chlorocomplexes, and the extractants retained their selective properties. Extraction with Kelex 100 from chloride solution increased the separation between zinc and cadmium, in comparison with sulphate solutions.     

Boundary layer model for char combustion and gasification

A non-steady boundary layer model is developed for numerical simulation of combustion and gasification of a single shrinking char particle. The model considers mass and energy conservation coupled with heterogeneous char reactions producing CO and homogeneous oxidation of CO to CO₂ in the boundary layer surrounding the char particle. Mass conservation includes accumulation, molecular diffusion, Stefan flow and generation by chemical reaction. Energy conservation includes radiation transfer at the particle surface and heat accumulation within the particle. Simulation results predict experimentally measured conversion and temperature profiles of a burning Spherocarb particle in a laminar flow reactor. Effects of bulk oxygen concentration and particle size on the combustion process are addressed. Predicted particle temperature is significantly affected by boundary layer combustion of CO to CO₂. With increasing particle size, char gasification to char combustion ratio increases, resulting in decreasing particle temperature and increasing peak boundary layer temperature.