Oxidation of Metals 

About: Oxidation of Metals is an academic journal published by Springer Science+Business Media. The journal publishes majorly in the area(s): Oxide & Alloy. It has an ISSN identifier of 0030-770X. Over the lifetime, 2616 publications have been published receiving 71116 citations.

Experimental observations in support of the dynamic-segregation theory to explain the reactive-element effect

Abstract: The addition of reactive elements can have a significant effect on the oxidation behavior of alumina- and chromia-forming alloys. A model has been developed to explain the effects associated with the addition of reactive elements that is based on the segregation of reactive-element ions to scale grain boundaries and the metal-oxide interface. Reactive-element ions use these interaces as pathways for diffusion from the metal substrate to the gas interface of the scale. The driving force for this outward diffusion is the oxygen potential gradient across the scale. Doping of the scale grain boundaries results in scale growth primarily by inward oxygen diffusion, while doping at the metal-oxide interface slows the growth of interfacial voids and thus improves scale adhesion.

Low-temperature oxidation

Abstract: Low-temperature oxidation is a reaction, occurring at or below room temperature, between a solid and a gas. It usually involves the combination of oxygen with metals, and it has the greatest commercial impact in the presence of moisture, as in corrosion. Cabrera and Mott put forward a theory of low-temperature oxidation, based on the assumption that cation migration occurs under the influence of a potential built up across the growing oxide film. Recent experimental results require that this theory be expanded to explain recent observations such as anion migration during oxide growth and the transition from the initial chemisorbed monolayer to a bulk, threedimensional oxide. The additional ideas put forward in the present paper may be summarized as follows. Low-temperature oxidation is controlled by the nature of the oxide; whether it is a network former or a modifier. A period of fast, linear oxidation is followed by a slow logarithmic reaction whose rate, in turn, can increase if the oxide film crystallizes to form grain boundaries. The initial fast oxidation is a continuation of the chemisorption process. Place exchange (anions and cations interchanging positions) occurs when the energy due to the image force of an oxygen ion is greater than the bond energy holding the ion in place. A stable film forms when this bond energy is greater than the image force energy. The oxygen ions formed on the oxide surface then set up a potential across the film. This potential provides the driving force for continued reaction. Oxide growth during this later stage is a slow, logarithmic process. A barrier to ion transport exists at the gas-oxide interface in the case of anion migration and at the metal-oxide interface in the case of cation migration. In both cases, the field built up across the oxide lowers the barrier sufficiently so that ion migration can occur. Network modifiers allow cation migration. The reaction rate is sensitive to crystallographic orientation of the metal, but not to oxygen pressure. A constant voltage is maintained across the film, so that the Cabrera-Mott theory explains the logarithmic kinetics. Network-forming oxides allow onion migration. The number of anions, and hence, the rate of reaction, is sensitive to oxygen pressure, but not crystallographic orientation of the metal substrate. Since the potential is a result of the mobile anions, the film tends to grow under constant field. The logarithmic kinetics then must be explained by an increasing activation energy for ion transport, as proposed by Eley and Wilkinson. The logarithmic growth rate can be increased by the presence of water vapor if the water introduces “dangling” bonds into an oxide network structure. Crystallization of the oxide film also increases its rate of growth and results in the formation of oxide islands.

The influence of alloying elements on the development and maintenance of protective scales

Abstract: Some of the important principles that determine the establishment, growth and long-term maintenance of protective Cr2O3, Al2O3 and SiO2 scales on hightemperature iron-, nickel- and cobalt-base alloys are reviewed and discussed. Emphasis is placed on the effects of alloying elements and other additions, such as third elements and reactive elements or oxide dispersions, on each of these processes. Particular attention is paid to transport processes in the scales and the importance of short-circuit paths. Some of the important parameters that influence the long-term mechanical stability of such scales are considered and evaluated.

Review of the High-Temperature Oxidation of Iron and Carbon Steels in Air or Oxygen

Abstract: This paper reviews previous studies on iron and steel oxidation in oxygen or air at high temperatures. Oxidation of iron at temperatures above 700°C follows the parabolic law with the development of a three-layered hematite/magnetite/wustite scale structure. However, at temperatures below 700°C, inconsistent results have been reported, and the scale structures are less regular, significantly affected by sample-preparation methods. Oxidation of carbon steel is generally slower than iron oxidation. For very short-time oxidation, the scale structures are similar to those formed on iron, but for longer-time oxidation, because of the less adherent nature, the scale structures developed are typically much more complex. Continuous-cooling conditions, after very short-time oxidation, favor the retention of an adherent scale, suggesting that the method proposed by Kofstad for deriving the rate constant using continuous cooling or heating-oxidation data is more appropriate for steel oxidation. Oxygen availability has certain effects on iron and steel oxidation. Under continuous cooling conditions, the final scale structure is found to be a function of the starting temperature for cooling and the cooling rate. Different scale structures develop across the width of a hot-rolled strip because of the varied oxygen availability and cooling rates at different locations.

Microstructure, adhesion and growth kinetics of protective scales on metals and alloys

Abstract: Currentunderstanding of the complex interrelationships among growth kinetics, microstructure, and adhesion of protective Cr2O3 and Al2O3 scales is critically reviewed. Similarities and differences in the behavior of these two systems are highlighted. The morphology of the alloy-scale interface appears to be a critical factor. Recent ideas are advanced to interpret the effect of oxygen-active elements on the development of a tortuous interface conducive to improved scale tenacity.