No description available.

An electrochemical investigation of the corrosion of iron and Fe18Cr based stainless steel alloys was undertaken with particular emphasis on the nucleation and growth of surface films. Chronoamperometry was shown to be a sensitive technique to investigate the initial stages of film formation and growth. In a variety of acidic (pH < 7), alkaline and alkaline cyanide electrolytes, providing dissolution of the substrate metal could occur rising current transients, similar to those reported in electrocrystallisation studies, were observed when the electrode was stepped to the appropriate potential. This indicated that at these potentials the surface film formed via the nucleation and growth of discrete nuclei. A significant aspect of this study was visual evidence of this nucleation and subsequent growth of the film provided by scanning electron microscopy which supported the electrochemical data and interpretation thereof. Existing electrocrystallisation models were used to evaluate the experimental rising current transients. While these models gave an indication as to the prevailing nucleation and growth mechanism, they were found to be inadequate in describing anodic oxide formation on an oxidising substrate. A qualitative model was proposed. In acidic electrolytes, rising chronoamperometric transients were observed for Fe, Cr and Fe18Cr at passive potentials and for FexCr (x = 16,18, 20,23% Cr) and alloys 444, 4732, 4733, 304L and 316L at transpassive potentials. The transients were shown to be sensitive to variations of potential, temperature, electrolyte and alloy composition. A systematic investigation of the influence of temperature (20 0 C - 1200 C) on the chronoamperometric, cyclic voltammetric and rotating ring - disc electrode behaviour of Fe in O.5M and 1.0M NaOH was also undertaken. In alkaline electrolytes, the formation of a duplex surface film was proposed, with x-ray photoelectron spectroscopy indicating that the protective base layer consisted of FeO while Fez03 and FeOOH constituted the upper layer. Base layer formation was favoured with increasing temperature and increasing hydroxide ion concentration of the electrolyte. Addition of OAM NaCN to O.5M and 1.0M NaOH had a marked effect on the electrochemistry of the system, with CN- inhibiting surface film formation, particularly of the upper layer. A mechanism for the oxidation of Fe in alkaline and alkaline cyanide electrolytes was proposed. / Thesis (Ph.D.)-University of Natal, 1994.

No description available.

No description available.

No description available.

Duplex stainless steels (DSS) with roughly equal amount of austenite and ferrite phases are being used in industries such as petrochemical and pulp and paper mills. However, many DSS grades have been reported to undergo corrosion and stress corrosion cracking in some aggressive environments such as chlorides and sulfide-containing caustic solutions. Although stress corrosion cracking of duplex stainless steels in chloride solution has been investigated and well documented in the literature, SCC mechanisms for DSS in caustic solutions were unknown. Microstructural changes and environmental factors, such as pH of the solution, temperature, and resulting electrochemical potential also influence the SCC susceptibility of duplex stainless steels. In this study, the role of material and environmental parameters on corrosion and stress corrosion cracking of duplex stainless steels in caustic solutions were investigated. Results showed that the austenite phase in the DSS is more susceptible to crack initiation and propagation in caustic environment, which is different from that in the low pH chloride environment where the ferrite phase is the more susceptible phase. This study also showed that alloy composition and microstructural changes in duplex stainless steels due to different heat treatments could affect their SCC susceptibility. Moreover, corrosion rates and SCC susceptibility of DSS was found to increase with addition of sulfide to caustic solutions. Corrosion films on DSS indicated that the metal sulfide compounds formed along with oxides at the metal surface in the presence of sulfide containing caustic environments made the steel susceptible to SCC initiations. The overall results from this study helped in understanding the mechanism of SCC in caustic solutions. Favorable slip systems in the austenite phase of DSS favors slip-induced local film damage thereby initiating a stress corrosion crack. Repeated film repassivation and breaking, followed by crack tip dissolution results in crack propagation in the austenite phase of DSS alloys. Result from this study will have a significant impact in terms of identifying the alloy compositions, fabrication processes, microstructures, and environmental conditions that may be avoided to mitigate corrosion and stress corrosion cracking of DSS in caustic solutions.

This research investigates the mechanism of transgranular stress corrosion cracking (TGSCC) on fuel transmission pipelines. This research proposes that in near-neutral pH environments, hydrogen can be generated by the dissociation of carbonic acid and the reaction of metal ions with bicarbonate solutions, significantly increasing the available hydrogen for diffusion into the pipeline steel. This research has shown that TGSCC of pipeline steels is possible in simple groundwater solutions containing bicarbonate ions and carbon dioxide. Microstructural characterization coupled with hydrogen permeation indicates that the level of strain in the microstructure has the most influence on hydrogen diffusivity. Hydrogen accumulation occurs preferentially in at high energy discontinuous interfaces such as inclusion interfaces. It was determined that a stress concentration is required to facilitate sufficient hydrogen accumulation in the pipeline steel in order to initiate TGSCC. It was discovered that these stress concentrations develop from inclusions falling out of the pipeline surface. Slow strain rate tests found that TGSCC occurred in a wide range of compositions and temperatures as long as near-neutral conditions were maintained. Microcracks ahead of the crack tip provide evidence of hydrogen in these cracking processes. Morphology of these microcracks indicates that cracks propagate by the coalescence of microcracks with the main crack tip. Further research findings, scientific impact, and potential future work are also discussed.

Thesis (Ph. D.)--Ohio State University, 2008. / Title from first page of PDF file. Includes bibliographical references (p. 160-164).

Mémoire (M. Sc.A.)--Université du Québec à Chicoutimi, 1991. / Document électronique également accessible en format PDF. CaQCU

Thesis (M.Sc. in Applied Science(Metallurgical Engineering))--University of Pretoria, 2008. / Abstract in English. Includes bibliographical references (leaves 67-69).