Metals high-temperature oxidation

Metallurgy. The strong affinity for oxygen and sulfur makes the rare-earth metals useflil in metallurgy (qv). Mischmetal acts as a trap for these Group 16 (VIA) elements, which are usually detrimental to the properties of steel (qv) or cast iron (qv). Resistance to high temperature oxidation and thermomechanical properties of several metals and alloys are thus significantly improved by the addition of small amounts of mischmetal or its siUcide (16,17). 

N. Birks and G. H. Meir, Introduction to High Temperature Oxidation of Metals, E. Arnold, London, 1983. 

Today, the air oxidation of toluene is the source of most of the world s synthetic benzaldehyde. Both vapor- and Hquid-phase air oxidation processes have been used. In the vapor-phase process, a mixture of air and toluene vapor is passed over a catalyst consisting of the oxides of uranium, molybdenum, or related metals. High temperatures and short contact times are essential to maximize yields. Small amounts of copper oxide maybe added to the catalyst mixture to reduce formation of by-product maleic anhydride. 

P. Kofstad. High Temperature Oxidation of Metals. J. Wiley Sons. New York (1966) TA 462. K57. 

In an ionizing solvent, the metal ion initially goes into solution but may then undergo a secondary reaction, combining with other ions present in the environment to form an insoluble molecular species such as rust or aluminum oxide. In high-temperature oxidation, the metal ion becomes part of the lattice of the oxide formed. 

Kofsted, P., High Temperature Oxidation of Metals, John Wiley, New York 0965) Kubaschewski, O. and Hopkins, B. F., Oxidation of Metals and Alloys, Butterworths, London... 

Harwood, J. J. (Ed.), The Metal Molybdenum (the protection of molybdenum against high temperature oxidation), American Society for Metals, Cleveland, Ohio (1958)... 

Since the paper by Pilling and Bedworth in 1923 much has been written about the mechanism and laws of growth of oxides on metals. These studies have greatly assisted the understanding of high-temperature oxidation, and the mathematical rate laws deduced in some cases make possible useful quantitative predictions. With alloy steels the oxide scales have a complex structure chromium steels owe much of their oxidation resistance to the presence of chromium oxide in the inner scale layer. Other elements can act in the same way, but it is their chromium content which in the main establishes the oxidation resistance of most heat-resisting steels. 

Scale a thick visible oxide film formed during the high-temperature oxidation of a metal (the distinction between a film and a scale cannot be defined precisely). 

Thermal treatment—Processes in which vapor-phase contaminants are destroyed via high-temperature oxidation the primary categories of thermal treatment used to treat MTBE and other oxygenates include thermal oxidation, which employs a flame to generate the high temperatures needed to oxidize contaminants, and catalytic oxidation, which employs lower temperatures in the presence of a catalyst (typically platinum, palladium, or other metal oxides) to destroy contaminants. 

Such hybrid molecules and supramolecular solids offer the promise of systems with the flexibility, strength, toughness, and ease of fabrication of polymers, with the high temperature oxidative stability of ceramics, and the electrical or catalytic properties of metals. Polyphosphazene chemistry provides an illustration of what is possible in one representative hybrid system. 

In the broadest sense, coordination chemistry is involved in the majority of steps prior to the isolation of a pure metal because the physical properties and relative stabilities of metal compounds relate to the nature and disposition of ligands in the metal coordination spheres. This applies both to pyrometallurgy, which produces metals or intermediate products directly from the ore by use of high-temperature oxidative or reductive processes and to hydrometallurgy, which involves the processing of an ore by the dissolution, separation, purification, and precipitation of the dissolved metal by the use of aqueous solutions. 4... 

His research interests are generally in high-temperature and solid-state chemistry of materials, including electrochemical devices (e.g., chemical sensors and fuel cells) and the chemical stability of materials (e.g., high-temperature oxidation). Dr. Fergus is an active member of the Electrochemical Society, the Metals, Minerals and Materials Society, the American Ceramics Society, the Materials Research Society, and the American Society for Engineering Education. 

Yttrium alloys have many applications. The metal doped with rare earths such as europium is used as phosphor for color television receivers. When added to iron, chromium, vanadium, niobium, and other metals it enhances resistance of these metals and their alloys to high temperature oxidation and recrystallization. It is a deoxidizer for vanadium and other nonferrous metals. Yttrium-aluminum garnets are used in lasers and in jewelery gemstones. Yttrium-iron garnets are used as transmitters and as transducers of acoustic energy. 

The conventional preparative routes to anionic, neutral, or cationic complexes of indium start with the metal, which is dissolved in a suitable mineral acid to give a solution from which hydrated salts can be obtained by evaporation. These hydrates react with a variety of neutral or anionic ligands in nonaqueous solvents, and a wide range of indium(III) complexes have been prepared in this manner.1 Alternatively, the direct high-temperature oxidation of the metal by halogens yields the anhydrous trihalides, which are again convenient starting materials in synthetic work. In the former case, the initial oxidation of the metal is followed by isolation, solution reaction, precipitation, and recrystallization. 

Gloom for Oxide Superconductors Dismayed at the progress through the years, even with the most promising room-temperature metallic, binary oxides, many scientists abandoned the search for new high temperature oxide superconductors. Also, it should be mentioned that a deep-rooted prejudice had developed which claimed that the BCS theory had imposed a maximum transition temperature limit of 25 K for all superconducting materials, and that this temperature had already been achieved in certain alloys of niobium. Some scientists, however, were steadfast in their determination to break this barrier, optimistic in their outlook, and they continued their search for this unusual phenomenon in other metallic oxide systems. 

In this edition, we have incorporated new material in all the chapters and updated references to the literature. New sections dealing with porous solids, fullerenes and related materials, metal nitrides, metal tellurides, molecular magnets and other organic materials have been added. Under preparative strategies, we have included new types of synthesis reported in the literature, specially those based on soft chemistry routes. We have a new section covering typical results from empirical theory and electron spectroscopy. There is a major section dealing with high-temperature oxide superconductors. We hope that this edition of the book will prove to be a useful text and reference work for all those interested in solid state chemistry and materials science. 

Finally, there are two special cases in which the rectilinear law is observed when the rate-controlling factor is the rate of supply of O2 and when the metal oxide is volatile at the temperature of oxidation. The latter case occurs in the high temperature oxidation of molybdenum, since M0O3 is quite volatile, and in this case dw/dt is negative. 

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