Self oscillation phenomena of turbulent jets in a channel

A new method based on the Coanda effect for self oscillation of a circular jet bounded by rectangular enclosure is suggested. The experiments in both air and water reveal regions of stable oscillation wherein relationships are obtained between the Strouhal number and the shape factor of the channel. This oscillation method can also be used to mix different liquids in a vessel. For such applications, an improvement of mixing by oscillation is shown by means of a residual concentration diagram for a salt solution.     

High-strength–high-modulus polyimide fibers II. Spinning and properties of fibers

The polyimides based on 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA) described in Part I of this series were dissolved in p-chlorophenol and spun into fibers using a coagulating bath of ethanol. The fibers as spun had in general low tenacities and low moduli, but a heat treatment at 300–500°C under tension produced a remarkable increase in strength and modulus, and fibers with a tensile strength of 26 g/den (3.1 GPa) and an initial modulus higher than 1,000 g/den (120 GPa) could be obtained. Thus, the annealed fibers of polyimides are comparable to aramid fibers in mechanical properties. To heating in air and in the saturated steam, the polyimide fibers showed higher resistance than the aramid fibers. The polyimide fibers surpassed the aramid fibers in resistance to acid treatment and ultraviolet (UV) irradiation, but were inferior in resistance to alkali treatment. The annealed fibers of polyimides displayed distinct X-ray diffraction patterns. The chain repeat distance of 20.5 Å determined on the fibers of polyimide prepared from BPDA and o-tolidine, and 20.6 Å determined on the fibers of polyimide derived from BPDA and 3,4′-diaminodiphenyl ether are reasonable when the dimensions of monomeric units and the shapes of the molecular chains are considered. The X-ray reflections of both polyimide fibers were indexed satisfactorily on the basis of postulated unit cells.     

Characterization of acylmono-, mono-, di-, tri- and tetraglycosylsterol and saponin in Adzuki bean (Vigna angularis) seeds

Five sterylglycosides (acylmono-, mono-, di tri- and tetraglycosylsterol) and a saponin were isolated from Adzuki beans and characterized. In the glycosylsterols, the principal component sterols were sitosterol and stigmasterol; the major sugar component was glucose. The glucose units were shown to be linked by β1,6-bonds. The three oligoglycosylsterols were shown to be gentiobiosylsterol, gentiotriosylsterol and gentiotetraosylsterol; the latter two are novel sterylglycosides. The saponin was identified as glucopyranosyl-(β1→2)-glucopyranurosyl-(β1→3′)-soyasapogenol B (Azukisaponin I) which had previously been found in Adzuki beans.     

Preparation and Characterization of Superconducting B1-Type Mo1-xNbxN Thin Films

Solid-solution thin films, Mo_1−xNb_xN, with B1 (NaCl) structure have been deposited on substrates at 450°C by reactive sputtering of composite targets with Mo and Nb metals in an equimolar Ar and N₂ gas mixture. The lattice parameter of the solid solution increased linearly with an increase of Nb content, x . The superconducting transition temperature, T _c, of the Mo-rich films ( x ≦ 0.12) was around 6 K, which was lower than that expected from theoretical prediction. The residual resistivity ratio, r =ρ(300 K)/ρ(20 K), of the films varied with x , and a minimum value of r was observed in the vicinity of x = 0.5.     

Application of rigid polyurethane integral-skin foams to thermal insulating unit cases for car air conditioners

Integral-skin foams of rigid polyurethane are sandwich structures consisting of a core layer of closed cells enclosed in rigid surface layers on both sides. We examined the layer composition of integral-skin foam with the objective of maximum flexural strength, and then studied possibilities of reconciling the strength and thermal insulating properties in housings for evaporators in car air conditioners; i.e., unit cases. This examination showed that the most practical density range (250 ≦ ρ_pall ≦ 500 kg/m³) provides vibratile resistance and thermal insulating properties. In actual car-running tests, a maximum 0.1 MPa stress was generated on unit cases with overall densities of 350 kg/m³, We found this to be 0.4% of the flexural strength of an integral-skin foam and 2% of the fatigue strength. In the forcible vibratile test, a stress of 0.5 to 1.0 MPa was generated at the resonance point of a unit case with 250 to 500 kg/m³ overall density. We found that these values are 2 to 5% of integral-skin foam's flexural strength and 10 to 25% of its fatigue strength. These values are of the same level as the conventional unit case made of polypropylene blended with talc. An integral-skin foam with an overall density of 250 kg/m³, nearly equal to half the weight of polypropylene, has the same level of resistance to vibration.     

Evaluation for the curing characteristics of phenolic molding compounds by rockwell hardness test at an elevated temperature

Rockwell hardness measurement at an elevated temperature has been proposed as an evaluation method for the curing characteristics of thermosetting molding compounds. This method is convenient and has a high accuracy over a wide range of curing, Using a cone indenter, the following advantages are brought about: a good correspondence with acetone extraction test, in showing the degree of cure of the internal part of a molding rather than that of the skin layer, and a higher sensitivity in measuring higher degrees of cure. On examining curing behavior of commercial phenolic molding compounds by this method, an inflection point was observed on a plot of the hardness vs log curing time. This critical point has been called “the minimum cure time”, beyond which the molding exhibits good physical properties.     

Radiation-induced graft copolymerization of butadiene to polyethylene and polypropylene

Polyethylene and polypropylene films were irradiated by γ-irradiation from a Co⁶⁰ source in butadiene gas flow and in liquid butaidne. Irradiating in the butadiene gas flow is particularly convenient because the gas state monomer is available directly and little homopolymer is produced. In this case, there is a retardative effect on the grafting near the surface of the film and the grafting rate shows the maximum values at 50–60°C. for high-density PE (PEH) and PP. Irradiating in the liquid butadiene decreases the retardative effect near the surface. The effect of dose rate I on the grafting rate Rp is represented by R_p ∞ I^1/4 in this case. The grafting rate is always higher in PEH than in low-density PE (PEL). Results of x-ray diffractometry and electron microscopy indicate that the grafting reaction occurs predominantly near the surface of the crystallite (lamella) of PE and the grafting rate is not affected by the overall crystallinity of the trunk polymer but by the configurational structure, such as the degree of branching or side-chain length.     

Metabolism of 12-ketooctadecanoic acid byEscherichia coli K-12 andCandida tropicalis

The mode of degradation of long chain keto acids by two microorganisms was investigated.Escherichia coli K-12 converted 12-ketooctadecanoic acid to 4-ketodecanoic acid, accumulating some amounts of intermediates, 10-ketohexadecanoic, 8-ketotetradecanoic and 6-ketododecanoic acids. In contrast,Candida tropicalis completely metabolized the keto acid with transient accumulation of the metabolites mentioned above. The difference between the metabolism byE. coli of hydroxy acid and keto acid is that 12-hydroxyoctadecanoic acid is degraded as far as 6-hydroxydodecanoic acid, while 12-ketooctadecanoic acid can be degraded as far as 4-ketodecanoic acid.     

Anion-induced conformational transition of poly(l-arginine) and its two homologues

The interaction of various anions with poly(l-arginine) and its two homologues, poly(l-homoarginine) and poly(l-α-amino-γ-guanidinobutyric acid), has been studied in the neutral pH region. These polypeptides were found to change their conformations from coil to helix due to I^?, ClO^?₄ and SCN^?, and among them poly(l-homoarginine) and poly(l-arginine) were found to change conformation at smaller concentrations of the anions than poly(l-lysine). The helix of poly(l-homoarginine) was induced in the lyotropic series of the counteranions. Using the van't Hoff enthalpies for the transition of the polypeptides and the transition enthalpies obtained from calorimetry, the various thermodynamic parameters of the transitions were calculated by use of a theory based on the non-specific and the specific binding interactions of the anions with the charged sites on the polypeptides. The binding constants of ClO^?₄ and SCN^? with poly(l-homoarginine) and poly(l-arginine) were found to be four times as large as those with poly(l-lysine). The free energy changes of the transitions from coil to helix of poly(l-homoarginine) and poly(l-arginine) were found to be more negative than that of poly(l-lysine). From these results, the guanidinium ion can be concluded to form easily the ion pair with the anions on the polymer surface, thus allowing poly(l-homoarginine) and poly(l-arginine) to change their conformations at smaller concentrations of the anions than poly(l-lysine).