Grain refinement and superplasticity of pipes processed by high-pressure sliding

ABSTRACT

The high-pressure sliding (HPS) process was applied for grain refinement of a pipe form of an Al-3wt%Mg-0.2wt%Sc alloy by developing two types of straining techniques (called in this study anvil sliding and mandrel sliding). To achieve a homogeneous microstructure throughout the cross-section of the pipe, the sample is rotated around the longitudinal axis every after sliding operation by introducing multi-pass technique, named multi-pass HPS (MP-HPS) as developed earlier for rods. The MP-HPS-processed sample shows ultrafine-grained structures with an average grain size of ～260 and ～300?nm after the HPS processing using anvil sliding and mandrel sliding. The samples also exhibit superplasticity with total elongations well more than 400%, respectively. A finite-element method is used to simulate the evolution of strain in the HPS processing and demonstrates that the simulation well represents the experimental results.     

Determination of atomistic deformation of tricalcium silicate paste with high-volume fly ash

We examined the effect of incorporating high-volume fly ash on the atomic arrangement and interatomic deformation behavior of calcium silicate hydrates in tricalcium silicate paste upon exposure to external forces. The interatomic structural changes and strains under compressive load were assessed using synchrotron in situ high-energy X-ray scattering-based atomic pair distribution function analysis. Three different types of strains, which were (a) macroscopic strains from gauges on the surfaces of specimen, (b) strains in a reciprocal space (Bragg peak shift), and (c) strains in real space (PDF peak shift), were compared to each other. All monitored and calculated strains for tricalcium silicate-fly ash (50 wt% fly ash) paste were compared with the counterparts of the pure tricalcium silicate paste. Pair distribution function analysis in the range of r < 10 Å indicated that the atomic arrangement of tricalcium silicate-fly ash was similar to that of synthetic calcium silicate hydrates followed by that of pure tricalcium silicate paste. Moreover, the pair distribution function refinement results revealed that the calcium silicate hydrate structure in tricalcium silicate-fly ash paste was similar to tobermorite 11 Å, unlike that in pure tricalcium silicate paste. The interatomic strain of tricalcium silicate-fly ash in the real space (r < 20 Å) was smaller than that of tricalcium silicate under compression, which suggested that the incompressibility of calcium silicate hydrates at atomistic scale was enhanced by the incorporation of fly ash into it. This was likely to be caused by the increased silicate polymerization of calcium silicate hydrates, which was attributed to the increase in the amount of silicate in their structure via the addition of fly ash.     

Homogeneous Strain Introduction Using Reciprocation Technique in High-Pressure Sliding

Metallurgical and Materials Transactions A - This study examines strain distribution occurring in the high-pressure sliding (HPS) processing for rods of pure Al and an AZ61 alloy. The strain...     

Effect of Zn, Ni and Fe Impurities on Bi2Sr1.6La0.4CuO6+��

We measured the change of T _c with the doping of the magnetic and nonmagnetic impurity in Bi₂Sr_1.6La_0.4CuO_6+?? (Bi2201). The reduction of T _c is about 20% in samples with Zn (1.1%), Ni (1.0%), and Fe (1.2%), and a slight difference was observed among these samples. We also observed the resonance peak at the Zn-impurity site by scanning tunneling spectroscopy at 4.2 K. The observed resonance peak showed the four-fold symmetry, and appeared at approximately ?1.5 meV.     

Effect of alkali and alkaline-earth chloride addition on electrolytic reduction of UO2 in LiCl salt bath

The electrolytic reduction process of actinide oxides in a LiCl salt bath at 923 K has been developed for nuclear fuel reprocessing. Since some salt-soluble fission products, such as Cs, Sr and Ba, accumulate in the LiCl salt bath, their effect on UO₂ reduction was investigated. In the experiments, UO₂ specimens were reduced by potential- or current-controlled electrolysis in various LiCl salt baths containing up to 30 mol% of KCl, CsCl, SrCl₂ or BaCl₂. The rate of UO₂ reduction in a LiCl salt bath was considerably decreased by the addition of alkali metal chlorides (KCl and CsCl) and slightly decreased by BaCl₂ addition. SrCl₂ addition had no appreciable effect. It was suggested that the diffusion of O²⁻ ions from the inside of UO₂ specimens to the bulk salt determined the reduction rate during the electrolysis and that the effect of salt composition was related to the solubility of O²⁻ ions in the salt bath.     

Experimental investigation on self-leveling behavior in debris beds

During a hypothetical core-disruptive accident in a sodium-cooled fast breeder reactor, degraded core materials can form debris beds on the core-support structure and/or in the lower inlet plenum of the reactor vessel from rapid quenching and fragmentation of core material pool. Coolant boiling may lead ultimately to leveling of the debris bed that is crucial to the relocation of molten core and heat-removal capability of the debris bed. In the present study, we elected to use depressurization boiling to simulate an axially increasing void distribution in the debris bed. Bottom-heating boiling was also chosen to confirm that characteristics of the self-leveling process do not depend on the boiling mode. Particle size (between 0.5 and 6 mm), shape (spherical and non-spherical), bed volume (between 5 and 8 l) and density (namely of alumina, zirconia, lead and stainless steel) along with boiling intensity and total volume were taken as experimental parameters to obtain the general characteristics of the self-leveling process. A series of experiments with simulant materials were conducted and analyzed in detail. The good concordance of the transient processes obtained from the different boiling methods sufficiently demonstrates that the present results obtained using the depressurization boiling method exhibit these general self-leveling characteristics. Detailed comparisons of deduced time variations of the inclination angle provides qualitative tendencies based on the experimental parameters considered influential to self-leveling behavior. The rationale behind the definition introduced for equivalent power density is also presented.     

Scanning Tunneling Spectroscopy on Overdoped Bi2Sr2?xLaxCuO6+δ

We have performed low-temperature scanning tunneling spectroscopy on overdoped Bi₂Sr_2−x La _x CuO_6+δ (x=0.1 and 0.2) at 4.2 K. The tunneling spectra in both samples obviously exhibit two energy gaps: one has clear gap structure with sharp gap edge peaks, and another is observed as kinks inside the larger gap. Both the energy gaps inhomogeneously vary on the surface at nanometer scale, and their values positively correlate each other. The distributions of both gaps normalized to the mean values are identical independent of the doping level. These results suggest that the two gaps are commonly affected by the source of the electronic disorder.