Trays for gas-liquid contacting

A type of tray for gas-liquid contacting is described, in which the free area for gas flow through the tray is variable with and controlled by the gas flowrate. The property through which control of the free area is effected is the surface tension of the liquid phase. The advantages are the same as those of ballast and valve trays; namely, reduced pressure drop at high gas rates resulting in increased column capacity, and reduced free space at lower gas rates resulting in high mass transfer efficiency at low and medium vapor loadings as well. Tooling and production costs for the trays of the present investigation, however, are considerably lower than for ballast or valve trays or any other types which require machining operations in their fabrication, and are as low or lower than for sieve trays. Initial experimental comparisons with conventional trays demonstrated that the trays of the present investigation, although designed primarily for operation at high vapor loadings, were indeed capable of yielding high mass transfer efficiencies in the low-to-medium range of vapor loading     

Lipids in soil

As much as 20% of soil humus occurs in the form of lipids. High values are characteristic of Podzol soils and highmoor peats. Lipids of the following types are known to be present: paraffin hydrocarbons, phospholipids, fats, waxes, fatty acids, and terpenoids. A long list of compounds have been reported; the identification of many of them require confirmation using modern analytical techniques. Some of the lipids known to occur in soil have phytotoxic properties; these may have a depressing effect on seed germination and on root and shoot growth. Waxes and similar materials may be responsible for the difficultly wettable condition of certain sands.     

Adsorption isotherms of sesame oil in a concentrated miscella system

The adsorption of peroxides, unsaturated carbonyls, free fatty acids and carotenoids from unrefined sesame oil on vegetable carbon (5%, w/w) in a miscella system was studied. Three different solvent conditions (hexane/ethanol, 100:0, 95:5 and 75:25, vol/vol), combined in a factorial design with five levels of solvent (0, 10, 20, 30 and 40%, w/w), were used to develop the miscella. Equilibrium adsorption was not achieved during the 100 min of adsorption, mainly because the oil components were involved in oxidation reactions during the adsorption process. However, for a given solvent concentration, adsorption of the oil components showed a significant linear regression on their respective initial concentration in the miscella (C_i). Peroxides and carbonyls showed, at all solvent levels investigated, an affinity for the carbon more independent of their C_i than free fatty acids and carotenoids. In general, at the same C_i, a higher adsorption was achieved as solvent concentration increased. The results indicated that free fatty acid adsorption may depend on competitive adsorption based on molecule hydrophobicity. However, in spite of the higher hydrophobicity of carotenoids, compared with free fatty acids, they might not be competing for the same adsorbing sites. Ethanol showed a prooxidant effect that increased peroxide production during adsorption but did not affect the reaction involved in carbonyl production.     

Arylidene polymers. XVIII. Synthesis and thermal behavior of organometallic arylidene polyesters containing ferrocene derivatives in the main chain

A new interesting category of organometallic polyesters based on diarylidenecycloalkanones containing ferrocene derivatives in the polymer main chain has been prepared by interfacial polycondensation of 1,1′-dichlorocarbonyl ferrocene or 1,1′-dichlorocarbonyl-4,4′-diiodoferrocene with 2,5-bis(p-hydroxybenzylidene)cyclopentanone, 2,5-divanillylidenecyclopentanone, 2,6-bis(p-hydroxybenzylidene)cyclohexanone, 2,6-divanillylidenecyclohexanone, and 2,7-bis(p-hydroxybenzylidene) cycloheptanone. The resulting polyesters were characterized by elemental analyses, infrared spectroscopy, solubility, and viscometry measurements. The thermal behavior of the synthesized polymers was evaluated by thermal gravimetric analysis and correlated with their structures. The crystallinity of all polymers were examined by x-ray diffraction analysis. Moreover, the electrical conductivity of a selected example of polymer was investigated above the temperature range (300–500 K) and showed that it followed an Arrhenius-type equation with activation energy 2.09 eV. © 1993 John Wiley & Sons, Inc.     

Tensile properties of CaCO3-filled polyethylenes

Tensile stress–strain behavior and dilatation behavior of CaCO₃-filled linear polyethylenes with differing molecular weight was found to be dependent upon filler content, polymer filler interface, and polymer molecular weight. Electron microscopy of samples undergoing deformation revealed the presence of craze type deformation.     

Glass transition temperature and critical properties

In a preceding paper it was shown that for high molecular weight polymers, the volume of the repeating unit at T_g is proportional to the total free space defined as V_c?V₀ where V_c is the volume of the repeating unit at the critical temperature and V₀ is the volume of the repeating unit at absolute zero. Here it will be demonstrated that this proportionality is also true for a host of low molecular weight liquids. In addition, an empirical method of estimating T_c for a high molecular weight polymer is proposed which provides values of T_c which are consistent with those for low molecular weight liquids.     

Deposition of dense isotropic carbon from acetylene in fluidized bed

Pyrolytic carbon was deposited from acetylene in a fluidized bed at 1100°C on alumina microspheres. In case when only argon was used as the diluent gas, density and BAF of the deposit decreased and deposition yield increased with increasing acetylene concentration. Hydrogen sypply suppressed carbon formation and, consequently, caused an increase in density and Lc. BAF was relatively independent of hydrogen concentration. It was found that high density, isotropic carbon can be deposited from acetylene at 1100°C, if an appropriate proportion of hydrogen is added.     

Tensile strength of polyurethane exposed to nitrogen dioxide

Polyurethane prepared from tetramethylene glycol and diisocyanate was exposed in the form of films to small pressures of NO₂ and to NO₂ plus air. Tensile strength was measured as a function of exposure time and temperature with an apparatus especially constructed for the purpose of measuring mechanical properties in different environmental “atmospheres.”