Stress corrosion cracking of steels in industrial process environments

dc.contributor.advisorSandenbergh, R.F.
dc.contributor.postgraduateHeaver, Edward Ernest
dc.date.accessioned2013-12-10T08:44:05Z
dc.date.available2013-12-10T08:44:05Z
dc.date.created1994-11-05
dc.date.issued1994-11-20
dc.descriptionThesis (PhD (Metallurgy))--University of Pretoria, 1994.en_US
dc.description.abstractThe interactions between engineering materials and their environment which give rise to stress corrosion cracking are reviewed and industrial examples from the petrochemical industry are described. In one of the examples, cracking took place in carbon steel exposed to pressurised gas containing carbon monoxide, carbon dioxide and water. The crack morphology in this system was studied by metallography of samples from industrial gas processing plants and the crack growth rates were determined using precracked specimens. Constant extension rate tests, U-bend specimens and potentiodynamic studies were used to evaluate alternative materials and inhibitor additions in CO-C02-H20 environments. Electrochemical noise was accessed as a technique to monitor sec on line. It was found that the CO-C02-H20 system was characterised by a time dependent adsorption of carbon monoxide at anodic and cathodic sites. The adsorption produced a critical balance between crack tip corrosion rate and the repassivation process comparable to the behaviour at the active-passive transition zone in more conventional systems. The anodic passivation exhibited a breakdown potential near to -400 mV (Ag/ AgCI) that defined the zone of sec susceptibility. Inhibition by CO and hence sec was virtually independent of CO partial pressure provided there was a sufficient reservoir of CO. The addition of commercial film forming inhibitors did not greatly influence the system and sec was still observed in CO-C02-H20 environments to which inhibitors had been added. Steels containing alloy additions of more than 9 % chromium were found to be resistant to sec but austenitic-ferritic weld joints cracked. A low alloy 3% nickel steel performed well in the constant extension rate tests but was not wholly resistant to sec. The morphology of stress corrosion cracks in CO-C02-H20 mixtures was influenced by carbon monoxide partial pressure. More corrosion was observed on the crack walls at low carbon monoxide partial pressure and widened cracks resembling •mesa• corrosion were common. This increased corrosion was probably due to difficulty in maintaining passivity in the crevice formed by the growing crack. Similarly, crevicing in precracked specimens appeared to inhibit sec and no crack extension was observed. Electrochemical noise proved to be a useful tool for monitoring.en_US
dc.description.availabilityUnrestricteden_US
dc.description.degreePhD (Metallurgy)
dc.description.departmentMaterials Science and Metallurgical Engineeringen_US
dc.description.librariangm2013en_US
dc.identifier.citationHeaver, EE 1994, Stress corrosion cracking of steels in industrial process environments, PhD thesis, University of Pretoria, Pretoria, viewed yymmdd <http://hdl.handle.net/2263/32795>en_US
dc.identifier.otherD13/9/994/gmen_US
dc.identifier.urihttp://hdl.handle.net/2263/32795
dc.language.isoenen_US
dc.publisherUniversity of Pretoria
dc.rights© 1994 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.en_US
dc.subjectUCTDen_US
dc.subjectCarbon monoxide (CO)en_US
dc.subjectCarbon dioxideen_US
dc.subjectWateren_US
dc.subjectPrecracked specimensen_US
dc.subjectStress corrosion cracking
dc.titleStress corrosion cracking of steels in industrial process environmentsen_US
dc.typeThesisen_US

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