Transport of K in PVC matrix membranes containing valinomycin

We report impedance measurements on PVC matrix membranes which contain KBPh₄ with varying proportions of valinomycin. In agreement with our earlier measurements the value of the bulk membrane resistance (R_b) is much larger in the presence of valinomycin, indicating that the mobility of K⁺ is greatly reduced by the valinomycin. R_b shows a linear variation with valinomycin/K⁺ ratio between 0 and 1, but it is invariant at higher valinomycin/K⁺ ratios. Thus there is no evidence for a special transport mechanism for K⁺ in these membranes.     

Drying cellulose triacetate in a dryer with a vibrational fluidized bed

Conclusions The process of drying cellulose triacetate in a vibrating bed has been studied.For final drying of cellulose triacetate before solution, it is recommended to use an industrial specimen of a unit with a vibrating bed having a capacity of 2700 kg/h.This assembly can be used to dry other fibre-forming disperse polymeric materials containing strongly bound moisture.Translated from Khimicheskie Volokna, No. 3, pp. 49–51, May–June, 1984.     

Chemical changes in polyvinyl fluoride during the process of fibre-spinning

Conclusions The change in some properties of polyvinyl fluoride during the process of fibre spinning has been investigated.It has been found that during the process of converting PVF powder into fibre, the degree of polymer crystallinity plus its resistance to thermal and thermooxidative degradation is increased; depending on the spinning regime, the densities and physicomechanical properties of PVF fibres are different.Translated from Khimicheskie Volokna, No. 4, pp. 34–35, July–August, 1984.     

Unsaturated polyesters. II. Structure and properties of polyester resins based on cinnamylsuccinic acid

Unsaturated Polyester resins were prepared by the reaction of cinnamylsuccinic acid with saturated diols, namely, ethylene, diethylene, propylene, dipropylene, tetramethylene, and hexamethylene glycols, and the unsaturated diols, namely, 1,4-butene- and 1,4-butynediols. All the polyester resins obtained have been characterized and were found to cure with styrene, with relatively low conversions. The properties of the cured polyesters in the form of films were determined. IR and ¹H-NMR spectroscopy were used for both qualitative and quantitative analyses of the polyesters and their hydrolyzate products, after curing with styrene.     

NMR Line Shape-Spin-Lattice Relaxation Correlation Study of Portland Cement Hydration

The proton free induction decay of a portland cement paste in an advanced stage of hydration can be roughly divided into three main components: (1) a component with a very short spin-spin relaxation time, T², representing the protons of the solid OH groups and the water of crystallization, (2) a component with an intermediate T, representing the bonded water in the gel phase, and (3) a third component with a relatively long T² representing the water in the micropores and layers. The dependences of the intensities, T²'s, and spin-lattice relaxation times (T¹'s) of these three components on the cement hardening time have been determined. The proton spin-lattice relaxation time of the "solid" component increases with hardening time whereas T¹ decreases for the other two components. The observed time dependence of the diffusion coefficient, D, of water in a tricalcium silicate paste supports the findings of the above correlation study.     

Spalling of Flat Plates by Thermal Shock

A model is presented for the thermal shock damage in plates subjected to a sudden rise in temperature. Spalling is assumed to follow localized buckling caused by the thermally induced compressive stresses above subsurface flaws. The minimum size o flaw required to cause spalling is determined as a function of the material properties of the plate, the temperature rise, the position of the paw, and the time after the thermal shock.     

Phase Studies Concerning Sintering in Aluminas Doped with Ti4+

Previous solid state analyses of sintering in Ti⁴⁺-doped-commercial alumina are shown to be in error because a liquid phase exists in the appropriate region of the Al₂O₃−TiO₃−Na₂Ophase diagram at least by 1350^°C, a temperature lower than that at which "solid state" studies were conducted. It is suggested that liquid-phase sintering is a much more common occurrence than was realized formerly.     

Physical and chemical characteristics of butterfat fractions obtained by crystallization from molten fat

Both summer and winter butterfats were fractionated using a laboratory procedure which was designed to simulate a commercial fractionation process. The process is based on a slow, controlled cooling of the melted fat, a short stabilization time at the fractionation temperature, and separation of the crystals from the liquid oil by vacuum filtration using a stainless steel perforated disc. Fractionation temperatures of 29, 26, 23 and 19 C for winter butterfat and 29 and 19 C for summer butterfat were used to obtain solid and liquid fractions at each temperature. Three replications at each temperature showed good reproducibility of results. The fractions were characterized by their fatty acid and triglyceride compositions, melting and crystallization behavior, iodine value, peroxide value and melting point. Presented at the AOCS meeting in Philadelphia in May 1985.