Special features in dyeing modacrylic fibre

Conclusions The possibility of dyeing freshly-spun modacrylic fibre with cationic dyes and in bulk with dyes or pigments of various classes has been investigated under laboratory conditions.It is recommended to use dyeing of modacrylic fibre in bulk with acetone-soluble dyes, which permits one to eliminate the energy-intensive process of pigment dispersion.Translated from Khimicheskie Volokna, No. 6, p. 36, November–December, 1988.     

Über die Bildung des Kakaoaromas aus seinen Vorstufen

Formation of Cocoa Aroma from Its Precursors Isolation and chemical composition of a highly purified mixture of aroma-precursors from raw cocoa were extensively studied and the alterations due to heating at roasting temperatures were followed quantitatively. Cocoa aroma is formed in the course of a Maillard reaction between amino acids and reducing sugars. Participation of oligopeptides in the alterations that are specific for the process of roasting could be detected for the first time. From the high-boiling components present in the reaction product, a fraction having the typical cocoa flavour could be isolated and resolved by gas chromatography. The consequences of these observations on the technology of roasting of cocoa are discussed.     

Use of cascade reduction potential for selective precipitation of Au,Cu, and Pb in hydrochloric acid solution

Optimization of reduction potential for electroseparation was studied for the recovery of gold, copper, and lead from acidic solution. A linear sweep voltammetric method enabled us to determine characteristic reduction potentials for each metal and the kinetics of the metal deposition indicated by current-voltage curves. In order to precipitate the metal species sequentially, reduction potentials were examined for the individual and mixed solutions of Au(III), Cu(II), and Pb(II). The three metals were reasonably well isolated from the mixed solutions such as Cu(II)/ Pb(II) and Au(III)/Cu(II)/Pb(II) in the order of the corresponding reduction potentials, in particular, the mass transfer controlled reduction potentials, obtained from linear sweep voltammetry (LSV) measurement.     

Gas absorption in laminar falling films of pseudoplastic liquids

Gas absorption into laminar falling films of power-law liquids was studied theoretically and experimentally. The convective-diffusion equation was solved by the method of separation of variables and the analytical solution for the average Sherwood number was obtained as a function of the Graetz number and the power-law index of the liquid. Experiments were carried out on the absorption of pure carbon dioxide, hydrogen and helium into aqueous kaolin slurries by using a long wetted-wall column and the average absorption rates were measured as a function of the mass flow rate of the liquid. The experimental results were in good agreement with the theoretical predictions.     

Volatilization of components from zirconia ceramics

Conclusions We investigated volatilization in isothermal conditions of solid solutions of oxides of calcium and yttrium in ZrO₂.The calcium oxide is intensely sublimited from the solid solution of zirconium dioxide, stabilized with CaO at 2000–2100°C. However, during soaking and rapid cooling, destabilization does not occur, even during sublimation of 70–75% CaO. With rise in temperature to 2400–2500°C and a 4 h soak, only 0.5% CaO is preserved in the solid solution, which leads to destabilization and conversion of a large part of the cubic form of ZrO₂ with calcium oxide by fusion, we note sublimation of part of the CaO, and the remaining quantity (3%) is adequate for complete conversion of the zirconia into the stable cubic form.Volatilization of the stabilizing additive occurs in the form of YO at substantially higher temperatures than volatilization of the calcium oxide from the solid solution of zirconium dioxide, stabilized with yttrium oxide. Simultaneously with this we note volatilization of zirconium dioxide in the form of ZrO and ZrO₂.For the use of zirconium dioxide at elevated service temperatures, we would recommend yttrium oxide as a stabilizing additive.Translated from Ogneupory, No. 1, pp. 49–52, January, 1968.     

Direct Observation of Triplet Reactions of Anthraquinone Vat Dyes Using Nanosecond Laser Photolysis

The triplet-triplet spectra of three commercial anthraquinone vat dyes (C.I. 67300, C.I. 59100 and C.I. 60515) were studied in solution at room temperature using laser photolysis. The triplet states of these dyes react with oxygen, and the rate constants for the quenching process were measured, together with the rates of energy transfer from the triplet state to anthracene. These observations are considered in relation to the photoreactivity of these dyes.     

A thermomechanical investigation of highly cold-drawn polycarbonate

A new technique detecting molecular motions in drawn polymers was applied to highly cold-drawn polycarbonate of bisphenol A. It is shown that the sample exhibits thermal shrinkage in three steps with the temperature increase up to above the glass transition temperature. The molecular relaxation at the highest temperature is due to the glass transition. The other two molecular motions at the lower temperature are those of main chain in the glassy state and they correspond to the molecular motions as revealed in dielectric measurement by Sacher.¹ By using the general theory of the thermal analysis by Ozawa,² the apparent activation energies of these molecular motions were obtained: for the highest temperature 110 kcal/mole, and for the lowest temperature, 33.5 kcal/mole. The impact strength and the cold workability of this polymer are also discussed in relation to these molecular motions.     

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.