Thermodynamic properties and mixing thermodynamic parameters of Ba-Al, Mg-Al, Sr-Al and Cu-Al metallic melts

Application of equations of mixing thermodynamic parameters formulated on the basis of the coexistence theory of metallic melts in Ba-Al, Mg-Al, Sr-Al and Cu-Al melts leads to fruitful results that not only the evaluated mass action concentrations agree well with the measured activities, but also the calculated mixing thermodynamic parameters are quite coincident with the experimental values. Moreover, the calculated mass action concentrations strictly obey the mass action law. The evaluated mixing thermodynamic parameters have very fine regularity: the mixing free energy is composed of standard free formation energies of all compounds and chemical potentials of all structural units at equilibrium; the mixing enthalpy consists of standard formation enthalpies of all compounds; the mixing entropy is composed of standard entropies of all compounds and configuration entropies of all structural units at equilibrium. As the equations of mixing thermodynamic parameters formulated are widely applicable to metallic melts involving compound formation, they can be used as the second practical criterion to determine whether thermodynamic models of metallic melts are correctly formulated.     

Processing and oxidation of co-deposited Ni-Al coatings

Electrodeposited Ni matrix/Al microparticles or nanoparticles dispersed composite coatings (termed as EMCCs or ENCCs) are developed from a Ni-based electrolyte bath. The Al microparticles are in a size range of 1 -5 μm and the Al nanoparticles in an average size of 75 nm. The Al content in coatings increases with increase in the particle content in the bath. Particle size effect on the degree of codeposition is not significant. However, codeposition of Al nanoparticles instead of microparticles promotes more homogenous growth of Ni deposits on {111}, {200} and {220} planes. The oxidation at 1 050 ℃ of the as-deposited composite coatings shows that at a comparable Al content, ENCC of Ni-Al exhibits a better oxidation resistance than EMCC of Ni-Al due to the fast formation of an alumina scale during the transient stage of oxidation.     

Ce在铁基溶液中分别与Cu,P,Ti相互作用规律的研究SCIEI

Fe-Cu-Ce,Fe-P-Ce和Fe-Ti-Ce溶液的平衡产物是Ce_2O_2S,而不是Ce与Cu、P、Ti的金属间化合物。测定了Fe液中Ce_2O_2S=2[Ce]+[O]+2[S]反应的平衡常数和溶质之间的相互作用系数。Ce降低Cu和Ti在Fe液中的活度,增大其溶解度,同时增大P的活度,降低其溶解度。     

High-temperature oxidation of a rapidly solidified amorphous Ta-Ir alloy

The oxidation products formed at 500 and 700°C on an amorphous Ta-44.5 at% Ir alloy in an Ar-0.1% O₂ gas mixture were characterized using SEM, XRD, EPMA, TEM, STEM, AES, and XPS. Initially, a thin (3–4 nm) layer of Ta₂O₅ formed at the surface of the alloy. Continued growth of the Ta₂O₅, which occurred very rapidly, involved diffusion of oxygen anions from the Ta₂O₅/gas interface to the alloy/Ta₂O₅ interface, where tantalum was selectively oxidized. Because the oxide grew more quickly than iridium could diffuse back into the alloy, the iridium coalesced into platelets of crystalline iridium-rich alloy that were oriented approximately parallel to the oxide/alloy interface, and which became embedded in a matrix of Ta₂O₅. The unoxidized core remained in the glassy state. The oxidation process and/or the dissolution of oxygen into the unoxidized alloy caused the alloy to become embrittled.     

High-temperature oxidation of directionally solidified Ni-Cr-Nb-AI (γ/γ′-δ) eutectic alloys

The oxidation of Ni-23.1Nb-4.4Al and Ni-19.7Nb-6 Cr-2.5Al alloys in air at temperatures in the range 870–1100°C has been studied for times up to 168 hr, in the as-cast, slowly cooled, and directionally solidified forms. The oxidation rate decreases with increasing temperature for the ternary alloy, and this appears to be due to the increasing tendency to establish a continuous Al₂O₃ layer at the metal surface, although at no temperature in this range is a complete layer established. At the lowest temperature the -Ni₃Nb lamellae are preferentially oxidized, with fingers of oxide extending into the metal, but at 900°C and above a continuous single-phase 8-free layer is established at the metal surface very early in the oxidation. The oxidation rate of the quaternary alloy increases with increasing temperature. At the lower temperatures a continuous Al₂O₃ layer is established at the metal surface, but at the highest temperature the aluminum oxidizes internally and a continuous layer is not established, internal oxidation penetrating down the lamellae. It appears that niobium, like chromium, is able to promote the formation of external Al₂O₃ layers; if this fact is accepted, the beneficial role of chromium in these alloys is difficult to explain.     

Oxidation behavior of copper at high temperatures under two different modes of direct-current applications

Oxidation kinetics of copper in the temperature range of 973–1173 K atP _{O 2}=21.27 kPa exhibit enhancement and deceleration in the rates with changing polarity compared to normal oxidation under interrupted mode of directcurrent application. These conditions are achieved by connecting the oxidizing copper covered with an initially formed thin oxide film to the positive and negative terminal of a dc source, respectively. However, the influence of direction of the current is found to be opposite under uninterrupted mode of impressed current flow in the same temperature range. The effect of short-circuiting the metal to the outer oxide/air interface on the reaction kinetics is also reported. The rate of oxide-scale growth under normal condition, and two different modes of current applications as well as with shorting circuitry attachment conform to the parabolic growth law. The results pertaining to the two different modes of impressed current have been discussed considering both the phenomena of electrolysis of the oxide electrolyte and the polarization at the two phase boundaries. The enhancement and the reduction in rates under uninterrupted impressed current conditions are explained on the basis of increased and decreased average defect concentrations, respectively, within the oxide layer. The acceleration and deceleration in the rates under interrupted mode of current flow have been explained in the light of sustenance of a steeper and flatter electrochemical-potential gradient of defects, respectively, across the growing-oxide layer. The possible different responses of the metal/oxide and oxide/air interfaces to the impressed current brought into play by two different modes of current application, have enabled to display a better insight on the mechanistic aspects of scale growth under the influence of an externally applied current.     

Al_2O_3/TiB_2和Al_2O_3/TiB_2/SiC_W陶瓷复合材料在1300℃的氧化行为

研究了热压烧结工艺制备的Al2O3/TiB2和Al2O3/TiB2/SiCW陶瓷复合材料在1300℃的氧化行为用XRD、SEM、TEM/EDSA分析了材料氧化后的相组成及显微结构.结果表明:两种材料在1300℃空气中氧化30h内的氧化增重符合抛物线规律,SiC晶须的加入可明显改善Al2O3/TiB2材料的高温抗氧化性.     

Microcrack generation and its healing in the oxide scale formed on Fe-Cr alloys

Fe -base alloys containing 5, 10, and 20 wt. % Cr were oxidized in a stream of O₂ at 750 and 900°C up to 264 hr. A sulfur decoration method was applied to detect the cracks generated in the scale during oxidation. This method revealed frequent crack generation and its healing in the scale. In the case of low-Cr alloys, the cracks are filled up with newly formed Fe-rich oxide but may be regenerated during further oxidation. Cracks are generated in the scale on an Fe-20Cr alloy also, although this alloy is not so severely attacked because of rapid healing.     

Structures of ceramics coatings on steel fabricated by hot-dipping and micro-arc oxidation

Firstly, an aluminum coating was produced metallurgically on mild steel by hot-dipping, then an aluminum oxide coating was formed self-growingly from the aluminum coating by micro-arc oxidation treatment. The structures of the composite coatings were investigated by means of SEM, TEM and XRD. The results show that the composite coating consists of three layers which are Fe-Al alloy, aluminum coating and aluminum oxide orderly outward from the steel substrate. There are amorphous phases, k-Al2O3 and θ-Al2O3 mainly in the aluminum oxide.