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Slurry coating technique, as one of the most popular deposition methods, is widely used to produce various material coatings. This method includes two processes: spraying, brushing or dipping of slurry, and sintering heat treatment of the coated specimen. Superalloys and stainless steels are the most common materials used as either coating materials or substrate materials because of their excellent corrosion, wear, high-temperature and mechanical properties. This research is aimed at investigating the influence of the sintering heat treatment in the slurry coating process developed at Kennametal Stellite Inc. on the microstructure, hardness and wear behavior of superalloys and stainless steels. Low-carbon Stellite 22, cobalt-based Tribaloy T-400C, martensitic AISI 420 and AISI 440C stainless steels are studied in this research. The microstructure, hardness and wear resistance of these alloys before and after the heat treatment are investigated, stressing the influence of the heat treatment on these material characteristics. The hardness and wear tested are conducted on these alloys at both room temperature and at elevated temperatures. The worn surfaces of each specimen are analyzed using a Scanning Electron Microscope (SEM) with backscatter electron imaging (BEI) and energy dispersive X ray (EDX) spectrum. It is demonstrated that the heat treatment alters the microstructures of these alloys differently; it increases the hardness but affects the wear resistance more complexly than hardness. At room temperature, the wear resistance of these alloys is governed by their microstructures. However, at high temperatures, oxidation, resulting in formation of oxide films on the specimen surface, influences the wear resistance significantly.

In this research, the corrosion performance of two austenitic stainless steels, namely 316L and 254SMO, in concentrated acetic acid solutions containing bromide ions has been investigated. In this research, the influence of two different electrochemical surface treatments (electropolishing and nitric acid passivation) on the corrosion behaviour of 316L stainless steel immersed in 15.3M HAc with 18.7mM bromide ions at 900°C was examined. Also, attemptswere made to study the performance of three organic inhibitors in the same conditions. Corrosion rates are assessed both by weight loss, and linear polarisation resistance. Interfacial corrosion chemistry is further characterised by open circuit potential and potentiodynamic polarization measurements. Substrate morphology is elucidated with optical microscopy, including 3D surface profiling, and scanning electron microscopy. Also, X-ray photoelectron spectroscopy is employed to gain further insight into the quite differentcorrosion performances of 316L and 254SMO in 15.3M acetic acid with 18.7mM Br ions.It was found that 316L and 254SMO steels have good corrosion resistance and low corrosion rates in 11.9M-HAc-Br-. Increasing acid concentration to 15.3 M led to a dramatic increase in corrosion rate of 316L with clear evidence of uniform and pitting corrosion proceeding simultaneously. Notably, the step increase in OCP for 316L steel and 254SMO during immersion in 15.3M-HAc-Br- solution indicates sudden changes in corrosion activity of the steels. The step seen for the 254SMO in 15.3M-HAc-Br- is indicative of passivation which is also supported by the XPS results, as a stable passive film was observed on the surface of alloy over the immersion time. However, the step increase in the OCP observed for 316L in 15.3MHAc-Br- is not associated with a significant decrease in corrosion rate. An alternative explanation is that the step coincides with an increase in the importance of pitting due to the evolving surface structure.From the attempts which were made to improve the corrosion resistance of the 316L stainless steel in 15.3M-HAc-Br-, both electropolishing and nitric acid passivation treatments were not sufficient to give any noticeable protection from the aggressive solution. Also, no corrosion inhibition was achieved when the three organic inhibitors, BTA, TU and 2MBI were utilised.

Fatigue performance is one of the important mechanical properties which is hindering some of the additive manufacturing build structures. The main objective of this study is to investigate the fatigue life dependence of the 21-6-9 austenitic stainless-steel build using the laser powder bed fusion (LPBF) technique. The study is mainly focused on the fracture surface based on defects and the micro constituents, how they are related to the fatigue performance of the samples. 21 samples were build using optimized process parameters in which 9 of the samples were built-in vertical direction and the remaining 12 were built in the horizontal direction. Low cycle fatigue (LCF) testing was carried out with the samples with 2 conditions i.e., room temperature 24⁰C and 750 ⁰C. Before the specimens were subjected to testing the samples were stress relived at 600⁰C for 2 hours. Fractography was carried out on the fracture surface to pinpoint the initiation sites (concluded by analyzing the striations) and the cause of failure. Microstructural characterization was carried out in both the vertical and the horizontal direction of the build. The fatigue crack growth initiated from the surface where defects were present, when the cyclic loads were applied the stress concentration at these regions caused the crack initiation to take place. In some cases, the defect size was smaller at the initiation site, and that correlated to increased fatigue life. To optimize the fatigue life of LPBF built 21-6-9 is important to minimize the grain size. However, the absence of defects is crucial as well, as those typically are the weakest link. Therefore, minimizing those during the manufacturing is essential.

The feasibility of in-situ alloying of AISI 410L martensitic stainless steel with nitrogen during Nd-YAG laser cladding was investigated with the aim of achieving a nitrogen content of at least 0.08 wt% and fully martensitic microstructures in the final clad deposit. Two in-situ nitrogen alloying techniques were studied. In the first set of experiments, the absorption of nitrogen from nitrogen-rich gas atmospheres was studied. Laser cladding with commercially available AISI 410L powder was performed using nitrogen-rich shielding and carrier gas. A marginal increase in deposit nitrogen content was observed, with the clad deposit displaying low hardness and mostly ferritic microstructures. Poor nitrogen absorption from nitrogen-containing atmospheres during Nd-YAG laser cladding is generally attributed to the short thermal cycle and to suppression of plasma formation above the weld pool. In the remaining experiments, Si3N4 powder was investigated as an alternative source for nitrogen during cladding. The addition of Si3N4 to the AISI 410L powder feed resulted in clad microstructures consisted of columnar -ferrite grains with martensite on the grain boundaries, higher hardness and an increase in deposit nitrogen content (to a maximum of 0.064 wt% nitrogen). Higher nitrogen contents in the clad deposit, however, significantly increased the volume percentage porosity in the clad layer. This prompted an investigation into the feasibility of raising the nitrogen solubility of the alloy through additions of manganese and nickel to the powder feed. Thermodynamic modelling revealed that the addition of manganese to AISI 410L powder increases the nitrogen solubility limit due to its negative interaction parameter with nitrogen. The addition of up to 3.5 wt% manganese to AISI 410L powder containing Si3N4 significantly increased the nitrogen solubility in the deposit. A martensitic microstructure with 0.12 wt% nitrogen and a peak hardness of 410 HV was achieved without any adverse increase in porosity in the clad layer. The clad nitrogen content easily exceeded the minimum requirement of 0.08 wt%. High nickel concentrations in AISI 410L stainless steel expand the austenite phase field at the expense of -ferrite and alter the solidification mode from ferritic to austenitic-ferritic. The addition of up to 5.5 wt% nickel, or combinations of nickel and manganese, to the nitrogen-alloyed AISI 410L powder feed raised the deposit nitrogen content, but not to the same extent as those deposits alloyed with manganese only. Since more austenite is present on cooling in nickel-alloyed AISI 410L deposits, less nitrogen is rejected to the liquid phase on solidification, resulting in higher nitrogen contents and less porosity in the room temperature microstructures. The amount of dilution during single-track laser cladding is mainly influenced by the specific energy per unit mass delivered by the laser beam. The clad height is strongly influenced by the powder deposition rate, whereas the bead width is influenced by the wettability of the deposits during laser cladding. During multi-track cladding, the observed percentage porosity is a function of the aspect ratio of the individual beads making up the clad layer, the deposition rate and the clad height. High deposition rates result in thicker layers, increasing the distance that N2 gas bubbles have to travel to escape to the atmosphere, while a high aspect ratio favours interbead porosity. The results suggest that in-situ nitrogen alloying during laser cladding should preferably be performed at low deposition rates to ensure higher clad nitrogen contents and hardness, lower clad heights, less dilution and less porosity. / Dissertation (MEng)--University of Pretoria, 2016. / Materials Science and Metallurgical Engineering / MEng / Unrestricted