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Compacted oxide layer glaze
Additional recommended knowledge
A not often used definition of 'glaze' is the highly sintered compacted oxide layer formed due to the sliding of either two metallic surfaces (or sometimes a metal surface and ceramic surface) at very high temperatures (normally several hundred degrees Celsius) in oxidizing conditions. The sliding or tribological action generates oxide debris that can be compacted against one or both sliding surfaces and under the correct conditions of load, sliding speed and oxide chemistry as well as (high) temperature, sinter together to form a 'glaze' layer. The 'glaze' formed in such cases is actually a crystalline oxide, with a very small crystal or grain size having been shown to approach nano-scale levels. Such 'glaze' layers were originally thought to be amorphous oxides of the same form as ceramic glazes, hence the name 'glaze' is still currently used.
Such 'glazes' have attracted limited attention due to their ability to protect the metallic surfaces on which they may form, from wear under the high temperature conditions in which they are generated. This high temperature wear protection allows potential use at temperatures beyond the range of conventional hydrocarbon-based, silicone-based or even solid lubricants such as molybdenum disulfide (the latter useful up to about 450 °C short term). Once they form, little further damage occurs unless there is a dramatic change in sliding conditions.
Such 'glazes' work by providing a mechanically resistant layer, which prevents direct contact between the two sliding surfaces. For example, when two metals slide against each other, there can be a high degree of adhesion between the surfaces. The adhesion may be sufficient to result metallic transfer from one surface to the other (or removal and ejection of such material) - effectively adhesive wear. With the 'glaze' layer present, such severe adhesive interactions cannot occur and wear may be greatly reduced. The continued generation of oxidized debris during the more gradual wear that results can sustain the 'glaze' layer and maintain this low wear regime.
However, their potential application has been hampered as they have only successfully been formed under the very sliding conditions where they are meant to offer protection. A limited amount of sliding damage (referred to as 'run in wear') needs to occur before the oxides are generated and such 'glaze' layers can form. Efforts at encouraging their early formation have met with very limited success and the damage inflicted during the 'run in' period is one factor preventing this technique being used for practical applications.
As oxide generated is effectively the result of the tribochemical decay of one or both of the metallic (or ceramic) surfaces in contact, the study of compacted oxide layer glazes is sometimes referred to as part of the more general field of high temperature corrosion.
The generation of oxides during high temperature sliding wear does not automatically lead to the production of a compacted oxide layer 'glaze'. Under certain conditions (potentially due to incorrect conditions of sliding speed, load, temperature or oxide chemistry / composition), the oxide may not sinter together and instead the loose oxide debris may assist or enhance the removal of material by abrasive wear. A change in conditions may also see a switch from the formation of a loose, abrasive oxide to the formation of wear protective compacted oxide glaze layers and vice versa.
Due to the potential for wear protection at high temperatures beyond which conventional lubricants can be used, possible uses have been speculated in applications such as car engines, power generation and even aerospace, where there is an increasing demand for ever higher efficiency and thus operating temperature.
Compacted oxide layers at low temperature
Compacted oxide layers can form due to sliding at low temperatures and offer some wear protection, however, in the absence of heat as a driving force (either due to frictional heating or higher ambient temperature), they cannot sinter together to form more protective 'glaze' layers.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Compacted_oxide_layer_glaze". A list of authors is available in Wikipedia.|