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Microstructure and High-Temperature Oxidation Behavior of Cold Gas-sprayed Ni-Al2O3 Coatings

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Abstract

Cermet coatings are widely used for high-temperature industrial applications. This study investigates the effect of high-temperature oxidation on cold gas dynamic-sprayed Ni-Al2O3 coatings. For this purpose, high-temperature oxidation tests were performed at 520 and 640 °C. The selected exposure times were 24, 48, 72, 168, and 336 h. The microstructural evolution during exposure at high temperature was analyzed by scanning electron microscopy (SEM), energy-dispersive x-ray spectroscopy (EDX), and x-ray diffraction (XRD). The oxidation kinetics was estimated by thickness measurements. The results show that the coatings protect the substrates against oxidation. In order to study possible changes in the mechanical properties of the system, Vickers microhardness experiments on the coatings and on the 10CrMo9-10 steel substrates were conducted. It was observed that hardness decreased by exposing the specimens to high temperature.

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TiCNT-Ni-based cermets are attractive cutting tools because of the combination of high hardness and wear resistance with improved toughness and thermal shock resistance. The present work reports the effect of WC addition (0-15 wt.%) on the machining performance of TiCN-20 wt.% Ni cermets against boiler steel. The cutting force was measured on-line using dynamometer, with respect to varying cutting speed and feed rate, in dry and orthogonal cutting conditions. The principal aim of the present investigation is to evaluate the dominant mechanisms, responsible for material removal on the rake face of cermets, using SEM-EDS. The cutting performance of TiCN-Ni cermet is observed to improve with the addition of WC content upto 10 wt.%. While, the adhesion of tribochemical layer is dominant with limited WC content, the presence of abrasive grooves and pull-outs are observed for TiCN-20Ni cermets containing higher amount of WC (>10 wt.%).
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Material degradation at high temperatures takes place due to loss in mechanical properties with increase in temperature as well as due to the chemical interaction of metal with the environment. This chemical interaction is further sub-divided into oxidation, sulfidation, and hot corrosion. While oxidation leads to the formation of oxide, which can be deleterious if the oxide is fast growing and spalls extensively, however, if the scale formed is adherent, thin and slow growing, it provides protection to the base metal or alloy. Sulfidation is a much severe degradation process and several times faster than the oxidation. In many industrial environments, it is a mixed gas environment, leading to oxidation and sulfidation simultaneously. Hot corrosion is another degradation mechanism which is even more severe than the oxidation and the sulfidation. Here, oxidation/sulfidation occurs in the presence of a molten salt on the surface of the substrate. Related issues, such as role of defect structure, active element effect and stress generation, during oxide growth process, have also been discussed. Finally, a guide to material selection for high temperature application is presented.
Article
Al-Al(2)O(3) composite coatings were produced on AZ91D magnesium alloy substrates using kinetic metallization (KM), which is a special type of cold spray using a convergent barrel nozzle to attain sonic velocity. The effect of the volume fraction of Al(2)O(3) particles and KM spray temperatures on the microstructure, hardness of the composite coatings, the deposition efficiency, and the bond strength between the coating and substrate was studied. Results show that addition of Al(2)O(3) particles not only significantly improves the density of the coating, but also enhances the deposition efficiency to an optimum value. The bond strength of the composite coatings with the substrate was found to be much stronger than the coating itself, measured using a specially designed lug shear method. Furthermore, based on bond strength data and SEM analysis, higher Al(2)O(3) content resulted in a failure mode transition from adhesive failure to cohesive failure. This is considered a result of a competition between the strengthening of the ceramic reinforcing particles at the coating/substrate interface, and the weakening of coating cohesive strength due to an increase in the proportion of weaker Al-Al(2)O(3) bonds compared with stronger Al-Al bonds. Characterisation of the composite coating in terms of hardness, porosity and microstructure was also conducted. Crown Copyright