Microstructures and Vickers hardness of rapidly solidified Al-Cu alloys near the Al-Al2Cu equilibrium eutectic composition

Al-Cu alloys near the Al-Al₂Cu equilibrium eutectic composition were rapidly solidified by the single-roller method. Two-zone structures were observed in transverse sections of Al-24.8, 30.0, 32.7, 33.2, 37.0 and 40.3 mass % Cu alloy ribbons, which were interpreted on the basis of the difference in cooling rates and of the temperature gradients between the chilled and free-surface sides of the ribbons. Non-equilibrium eutectic structures, cellular and irregular lamellar, were seen at the chilled side because the alloy liquids were directionally solidified with coupled eutectic growth. The coupled zone of the Al-Cu alloy expanded over the composition range 24.8–40.3 mass % Cu by rapid solidification. Dendritic structures were formed at the unchilled side of Al-24.8, 30.0, 37.0 and 40.3 mass % Cu alloys. Vickers hardness values at the chilled side differed from those at the unchilled side due to the difference in the microstructure.     

Catalytic performance of K-promoted Rh/USY catalysts in preferential oxidation of CO in rich hydrogen

K-promoted Rh/USY (molar ratio: K/Rh=3) catalyst was found to exhibit high performance in preferential oxidation of CO in rich hydrogen. Such high performance was maintained in the presence of steam and CO₂. The CO oxidation activity of the K-Rh/USY catalyst was independent of the partial pressure of H₂, while the activity of the unpromoted Rh/USY catalyst was decreased significantly in hydrogen-rich stream. The effect of potassium addition on the catalyst structure was investigated and is discussed in terms of the differences in the catalytic performance.     

A new type of nanocomposite in tetragonal zirconia polycrystal-molybdenum system

A ceramic/metal nanocomposite in tetragonal zirconia-molybdenum system possesses a novel microstructural feature composed of a mutual intragranular nanostructure, in which either nanometer sized Mo particles or equivalent sized zirconia particles are located within the zirconia grains or Mo grains, respectively. It achieves a simultaneous improvement in strength and toughness that overcomes the strength-toughness tradeoff relation.     

Tactic poly(crown ether)s with pendant benzocrown ethers

Summary Tactic and atactic poly(crown ether)s, poly(methacryloyloxymethylbenzo-15-crown-5), were synthesized by polymer reaction of the respective poly(methacrylic acid) with chloromethylbenzo-15-crown-5 and radical polymerization of methacryloyloxymethylbenzo-15-crown-5. By solvent extraction of alkali metal picrates with these poly(crown ether)s, the isotactic poly(crown ether) was found to be a little more selective for K⁺ and Rb⁺ than the syndiotactic and atactic ones.     

Electron spin resonance study of Langmuir-Blodgett films of N-docosylpyridinium- di(tetracyanoquinodimethane)

An electron spin resonance (ESR) investigation is performed on Langmuir-Blodgett films consisting of a surface-active 1:2 complex of N-docosylpyridinium and tetracyanoquinodimethane (TCNQ), whose temperature-dependent spin susceptibility has been so far found to be consistent with the random-exchange Heisenberg antiferromagnetic chain (REHAC) model of Soos and Bondeson. An out-of-plane anisotropy in the ESR spectra shows that the long axes of TCNQ molecules are preferentially oriented along the plane normal to the sample, where the negligible in- plane anisotropy indicates the random distribution of the short and the pπ orbital axes in the film plane. A heat treatment applied to the samples results in an increase in the concentration of disorder, showing the possibility of controlling it in the present REHAC system.     

Redox reaction of tri(2-deoxy-2-L-ascorbyl)amine. Formation of a persisting free radical species in water

Electrochemical studies showed that tri(2-deoxy-2-L-ascorbyl)amine ($\text{1}$), a new compound isolated as one of the products of reaction of dehydro-L-ascorbic acid with phenylalanine (with added L-ascorbic acid) in ethanol, is oxidized in aqueous solution in two reversible one-electron transfer steps, on mercury or platinum electrode. The first step occurs through the dianion, and its product is an unusually stable blue anion radical giving a characteristic ESR signal. The product of the second step of oxidation is labile and is slowly converted into the oxidized form of di(2-deoxy-2-L-ascorbyl)amine, presumably by hydrolysis with splitting of L-ascorbic acid.     

Repetition bend properties of Cu-Cr and Cu-Cr-Sn alloys

Repetition numbers of bending of Cu-0.81 wt% Cr, Cu-0.81 wt% Cr-0.14 wt% Sn and Cu-0.26 wt% Cr-0.10 wt% Sn alloys were investigated. After solution treatment, the first two types of copper alloys have a primary chromium phase; this is not so in the last alloy. The primary chromium phase does not influence the repetition numbers of bending of cold-rolled specimens; the repetition numbers of bending of specimens aged at 723 K for 1.8 × 10³ sec after cold rolling are higher than those of cold-rolled specimens. The cause of this is considered to be a recovery of work-hardening during ageing.