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Corrosion Studies of Duplex Stainless Steels with Micrometer Resolution
KTH, Skolan för kemivetenskap (CHE), Kemi, Korrosionslära.
KTH, Skolan för kemivetenskap (CHE), Kemi, Korrosionslära.ORCID-id: 0000-0002-4431-0671
KTH, Skolan för kemivetenskap (CHE), Kemi, Korrosionslära.ORCID-id: 0000-0002-9453-1333
2004 (Engelska)Ingår i: Journal of Corrosion Science & Engineering, ISSN 1466-8858, E-ISSN 1466-8858, Vol. 6, s. paper 28-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The local corrosion behavior of duplex stainless steel (DSS) is affected by a wide variety of factors. Localized corrosion of DSS frequently starts at micrometer scale inclusions or precipitates, which are often segregated in the austenite-ferrite boundary regions. Moreover, due to the partitioning of the key alloying elements of ferrite (Cr and Mo) and austenite (N and Ni), the local interactions between the phases must also be considered. The aim of this doctoral study was to increase the knowledge about the local dissolution behavior of DSS in acidic-chloride environments. The recent developments of new local probing techniques have opened a new frontier in corrosion science, providing valuable local information not accessible in the past. The local techniques used include electrochemical scanning tunneling microscopy (EC-STM), scanning probe force microscopy (SKPFM), magnetic force microscopy (MFM), and scanning Auger electron Spectroscopy (SAES), all with micrometer or sub-micrometer resolution. With EC-STM, it was possible to monitor local dissolution processes on DSS in situ, and in real time. MFM was capable of imaging the phase distribution in DSS without the need of the traditional surface etching, while SKPFM revealed that the Volta potential difference between the two phases was measurable and significant. SAES showed that the composition gradient at the phase boundaries is narrower than 2 µm. Different types of DSSs have been studied, from low-alloyed DSS to superduplex. Higher contents of Cr, Mo and N strengthened both phases as well as the phase boundaries, resulting in phases having similar corrosion resistance that showed a more uniform dissolution behavior. However, the Volta potential difference between the phases proved to be of the same order for all the DSSs studied. Austenite was in general associated to regions displaying a more noble Volta potential than ferrite, resulting in a higher dissolution rate of the ferrite next to the austenite phase.

Ort, förlag, år, upplaga, sidor
2004. Vol. 6, s. paper 28-
Nationell ämneskategori
Annan kemi Kemiteknik Kemi Kemi
Identifikatorer
URN: urn:nbn:se:kth:diva-78005OAI: oai:DiVA.org:kth-78005DiVA, id: diva2:492279
Anmärkning
QC 20120217Tillgänglig från: 2012-02-07 Skapad: 2012-02-07 Senast uppdaterad: 2017-12-08Bibliografiskt granskad

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Femenia, MarcPan, JinshanLeygraf, Christofer
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