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41.
Effect of vanadium and chromium on the microstructural features of V–Cr–Mn–Ni spheroidal carbide cast irons 总被引:2,自引:0,他引:2
V.G.Efremenko ;K.Shimizu ;A.P.Cheiliakh ;T.V.Kozarevskaya ;K.Kusumoto ;K.Yamamoto 《北京科技大学学报(英文版)》2014,(11):1096-1108
The objective of this investigation is to study the influence of vanadium(5.0wt%–10.0wt%) and chromium(0–9.0wt%) on the microstructure and hardness of Cr-V-Mn-Ni white cast irons with spheroidal vanadium carbides. The alloys' microstructural features are presented and discussed with regard to the distribution of phase elements. The structural constituents of the alloys are spheroidal VC, proeutectoid cementite, ledeburite eutectic, rosette-shaped carbide eutectic(based on M7C3), pearlite, martensite, and austenite. Their combinations and area fraction(AF) ratios are reported to be influenced by the alloys' chemical composition. Spheroidized VC particles are found to be sites for the nucleation of carbide eutectics. Cr and V are shown to substitute each other in the VC and M7C3 carbides, respectively. Chromium alloying leads to the formation of a eutectic(γ-Fe + М7С3), preventing the appearance of proeutectoid cementite in the structure. Vanadium and chromium are revealed to increase the total carbide fraction and the amount of austenite in the matrix. Cr is observed to play a key role in controlling the metallic matrix microstructure. 相似文献
42.
A mechanism of formation of copper nanoparticles is proposed for alkaline etching of a sputtering-deposited Al-30 at.%Cu alloy, simulating the equilibrium θ phase of 2000 series aluminium alloys. Their formation involves enrichment of copper in the alloy beneath a thin alumina film, clustering of copper atoms, and occlusion of the clusters, due to growth of alumina around the clusters, to form nanoparticles. The proposed mechanism is supported by medium energy ion scattering, Rutherford backscattering spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscopy of the alloy following immersion in the sodium hydroxide solution, which disclose the enrichment of copper and the generation of the nanoparticles in the etching product of hydrated alumina. The generation of the nanoparticles is dependent upon the enrichment of copper in the alloy in a layer of a few nanometres thickness, with no requirement for bulk de-alloying of the alloy. 相似文献
43.
Anodizing of solid-solution Al-1at.%Cu alloy in ammonium pentaborate electrolyte is shown to develop two distinct types of amorphous film. On alloy grains of {1 0 0} orientation, the alumina film is of uniform thickness and relatively featureless. For other grains, the film is of non-uniform thickness and contains oxygen bubbles. In both cases, copper species are distributed throughout the film. Copper is enriched in the alloy to ∼5.8×1015 Cu atoms cm−2 for bubble-free grains, with similar or slightly lower levels for other grains. Evidently, copper enrichment alone does not lead to generation of oxygen. Other factors suggested to be involved, each dependent upon grain orientation, are the structure of the enriched alloy layer, the cyclic nature of the oxidation of copper, and the generation of modulated film compositions. 相似文献
44.
Initial stages of plasma electrolytic oxidation of titanium 总被引:1,自引:0,他引:1
T. H. Teh A. Berkani S. Mato P. Skeldon G. E. Thompson H. Habazaki K. Shimizu 《Corrosion Science》2003,45(12):2757-2768
The initial stages of oxide growth on titanium are examined in a recently developed commercial alkaline pyrophosphate/aluminate electrolyte of interest for plasma electrolytic oxidation of light metal alloys. Constant current anodizing was employed, with resultant films examined by scanning and transmission electron microscopies and Rutherford backscattering spectroscopy. The initial film is relatively uniform and composed of TiO2, with low concentrations of aluminium and phosphorus species incorporated from the electrolyte. With increase in voltage the film breaks down locally, and regions of original and modified film develop simultaneously, with the latter occupying more of the surface as the voltage rises. Porous regions due to dielectric breakdown also become increasingly evident. At 240 V, sparking commences, and the surface reveals extensive, relatively uniform porosity, with the coating now containing much enhanced concentrations of aluminium and phosphorus species compared with the coating at lower voltages. The films develop at low efficiency due to generation of oxygen. The oxygen is produced within the original film material and at sites of dielectric breakdown. The former type of film develops a two-layered morphology, with an outer layer of amorphous TiO2 and an inner layer with numerous fine and course cavities. The cavities are due to the generation of oxygen that may be associated with the formation of anatase in the inner layer. 相似文献
45.
High-temperature strength and thermal stability of a unidirectionally solidified Al2O3/YAG eutectic composite 总被引:1,自引:0,他引:1
Y Waku N Nakagawa T Wakamoto H Ohtsubo K Shimizu Y Kohtoku 《Journal of Materials Science》1998,33(5):1217-1225
A unidirectional solidification method was investigated to manufacture Al2O3/YAG eutectic composites with high-temperature resistance that would make them usable at very high temperatures. We were successful in manufacturing a single-crystal Al2O3/single-crystal YAG eutectic composite with a dimension of 40 mm in diameter and 70 mm in length containing no colonies or pores. This composite also displayed excellent high-temperature strength characteristics. The flexural strength was in the range 350400 MPa from room temperature up to 2073 K (just below its melting point of about 2100 K) with no apparent temperature dependence. During tensile tests above 1923 K, the eutectic composite showed evidence of plastic deformation occurring by dislocation motion, and a yield phenomenon similar to many metals was observed. In addition, the microstructure of the composite was extremely stable: after 1000 h of heat treatment at 1973 K in an air atmosphere there was no growth. The above superior high-temperature characteristics are caused by such factors as the eutectic composite having a single-crystal Al2O3/single-crystal YAG structure, the formation of a compatible interface with no amorphous phase and thermal stability, and the combined effect of a YAG phase with superior high-temperature characteristics. © 1998 Chapman & Hall 相似文献
46.
Oda T. Kato T. Takahashi T. Shimizu K. 《Industry Applications, IEEE Transactions on》1998,34(2):268-272
Catalyst (copper-coated zeolite catalyst, i.e., Cu-ZSM-5) was used to enhance NOx removal plasma chemical reactions. Two kinds of hydrocarbons (2-propane-1-ol, 2-propanol) were added to the synthesized flue gas before the nonthermal plasma process, and their effects on NOx removal characteristics were investigated. Enhancement effects of NOx removal by the nonthermal plasma process with hydrocarbons as the additives were confirmed. Usually, the catalyst's working temperature is much higher than the room temperature. A catalytic reactor was installed after the plasma reactor. Catalytic effects on NOx removal characteristics disappeared when the synthesized flue gas temperature was increased (~250°C). When the synthesized flue gas temperature was at room temperature, about 90% NO x removal efficiency was realized with a combination of hydrocarbons, the catalytic reactor, and the pulsed discharge plasma 相似文献
47.
A theory recently developed by the present authors is applied to the study of the effect of elastic energy due to atomic size factor on the transformation behaviour of binary solid solutions. lt is found that elastic interaction energy (EIE), which is a part of the total elastic energy plays a key role in both ordering elastic interaction ordering (EIO) and spinodal decomposition. The present study gives a reasonable explanation to the historical dilemmas, "elastic energy paradox" and "atomic size factor paradox . By solving these confusing problems, the coexistence of ordering (EIO) and decomposition, which has been regarded as impossible by conventional theories. can be well understood. The mechanism is as follows: lowering of elastic energy demands EIO, and such an ordering provides a driving force for spinodal decomposition. Therefore, in alloys with large atomic size factor, spinodal decomposition is preceded and induced by ordering. Ordering and spinodal decomposition are thus closely related processes to each other 相似文献
48.
49.
Peculiar dendritic deposits of mercury were obtained galvanostatically from the mercurous nitratemethanol-water system at –50° C. These deposits could not be maintained at a constant shape because, when the current was interrupted, they transformed and shrank immediately to a spherical shape with hydrogen evolution. It seems that when the electrical potential was removed, the mercury deposits liquefied and the hydrogen stored in them was released during the period of shrinking. 相似文献
50.
Electron and nuclear transitions in the nuclear excitation by electron transition (NEET) process have been investigated. The NEET transitions for nuclei are presented in a table in which the electron and nuclear transitions, their transition energies, transition multipoles, and nuclear spin angular momentum are given. The elements are listed for which the difference between the electron and nuclear transition energy is <5 keV, because the NEET probability will be appreciable if the electron transition energy is close to the nuclear transition one. As both the experimental and theoretical studies for NEET are at an early stage, only the elements and their parameters related to NEET are listed here. The present compilation, however, provides a useful direction for future studies of NEET and its applications to nuclear science. 相似文献