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Metallic bond coating

Sprayed ceramic coatings can be made chemically active by selection of the spray parameters, which result in metastable phases within the coating. Ceramic bond coats are useful for difficult to bond materials such as ceramic components, including carbide-containing parts and refractory metals. These materials may be used in combination with a metallic bond coat on metallic substrates to mitigate stress differentials between the metallic substrate and the ceramic bond coat due to thermal or mechanical stress. [Pg.542]

The test is shown schematically in Figure 8.17. The indenter penetrates the TBC and oxide layers, and plastically deforms the metallic bond coat and substrate below. As illustrated in Figure 8.18 (viewed from above), this induces an axisymmetric debonding of the TBC and oxide layers similar to that for a thermally induced failure by buckling. [Pg.230]

Usually, a TBC system has a four-layered structure the ceramic thermal barrier layer, the metallic bond coat layer, a thermally grown oxide (TGO) layer between the topcoat and bond coat, and substrate. Each layer has its own specific physical and chemical properties, which provide the required functions in TBC. [Pg.476]

The ceramic thermal barrier layer provides thermal protection to the underlying materials. Also, this layer works as a shield to protect the underlying metallic parts from erosion and corrosion. The metallic bond coat is to protect the underlying superaUoy substrate from oxidation, balance thermal mismatch between the topcoat and substrate, and prevent interdiffusion of elements in the substrate and bond coat. [Pg.476]

Great efforts have been invested in searching for new ceramic materials with better performance than the current YSZ. Investigation into new metallic bond coat materials, which will be oxidation-resistant at 1473 K and smartly adaptive to the environments, has been urged to keep in accordance with the new ceramic materials and the new-generation single crystal superalloys. [Pg.489]

The wide range of soHd lubricants can generally be classified as either inorganic compounds or organic polymers, both commonly used in a bonded coating on a matching substrate, plus chemical conversion coatings and metal films. Since solid-film lubricants often suffer from poor wear resistance and inabihty to self-heal any breaks in the film, search continues for improved compositions. [Pg.249]

Lap shear samples performed according to ASTM-D1002 or D3163. Oily metal was coated with hexadecane. All other substrates were bonded unprepared. [Pg.842]

The practical result of epitaxy is a very high degree of adhesion between coating and substrate. The force needed to separate the interface is similar to that needed to break the metals on either side. Where a true metallic bond forms at an epitaxial interface it is only possible to measure adhesion if the bond is the weakest of the three near the interface. An adhesion test based on breaking the joint indicates only which of the three is weakest. For practical purposes any epitaxial joint will have a strength more than adequate for service conditions. [Pg.357]

Good adhesion to the metal. The coating must have an excellent bond to steel. Priming systems are frequently used to assist adhesion. [Pg.658]

In reinforcing materials double-dipped polyesters for improved tire durability, plasma-treated yams for improved bonding in tire, and increased usage of aramid fabric as belt and application of PEN are the areas where manufacturers are showing interest. Introduction of new styles of steel wire geometry for improved mbber to metal adhesion and new steel wire coating formulations for improved mbber to metal bonding are other focused areas of development. [Pg.931]

All adhesion scientists will agree that water is a very destructive environment for metal/polymer adhesion systems (see Fig. 5). Since water is one of the most commoi environments encountered, the effectiveness of metal/polymer coating and structural bonding systems has been severely limited by this great loss of adhesion strength in the presence of water. [Pg.43]

In summary, LME in my view is due to the upsetting of the Ratio of covalent bond to metallic band and resulting in an increased difficulty in the creation of free radicals. This takes away the ductility and results in brittleness. In this context, one can venture to predict that if solid metal is coated with a liquid metal whose electron density is less than that in solid metal, solid metal may become free electrondeficient and may actually facilitate the creation of free radicals. In this case an enductilement may result in lieu of embrittlement. [Pg.172]


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See also in sourсe #XX -- [ Pg.371 ]




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