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dc.contributor.authorSolem, Cathrine Kyung Won
dc.contributor.authorVullum, Per Erik
dc.contributor.authorTranell, Gabriella
dc.contributor.authorAune, Ragnhild Elizabeth
dc.date.accessioned2022-04-21T08:11:56Z
dc.date.available2022-04-21T08:11:56Z
dc.date.created2022-03-22T15:08:35Z
dc.date.issued2022
dc.identifier.citationLight Metals. 2022, 587-593.en_US
dc.identifier.issn0147-0809
dc.identifier.urihttps://hdl.handle.net/11250/2991834
dc.description.abstractOxidation of liquid aluminum (Al) during processing is a widely known problem, and magnesium (Mg), as a common alloying element, increases the oxidation rate of the alloy. It has been established that small additions of CO2 (≥ 4%) in an oxidizing atmosphere have a significant inhibiting effect on the rate of oxidation of Al alloys 5182 (AlMg4.5Mn0.4) and 6016 (AlSi1.2Mg0.4) discs based on oxide layer thickness and mass gain when heat-treated at 750 °C for 7 h. The phases present in the oxide layers for each alloy have now been identified and compared with discs heated in synthetic air and argon (Ar) under the same experimental conditions. The XRD analyses revealed the presence of MgO for all Al alloy 5182 discs, in addition to MgAl2O4 and Al2O3 when heated in synthetic air, and Mg2C3 when heated in the mixed cover gas containing 4% CO2. The low Mg-containing Al alloy 6016 revealed the presence of MgAl2O4 for all discs, in addition to MgO when heat-treated in the mixed cover gas containing 4% CO2, as well as Al2O3 when heated in Ar. For both alloys, Transmission Electron Microscopy (TEM) combined with Energy Dispersive X-ray Spectroscopy and Electron Energy Loss Spectroscopy (EDS-EELS) analyses revealed that the mixed cover gas also resulted in a nanometer-thin amorphous C layer, never previously detected, on top of the thin nanocrystalline MgO layer, retarding the evaporation of Mg and inhibiting the oxidation rate for both alloys.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.titleHeat Treatment of Mg-Containing Aluminum Alloys 5182 and 6016 in an Oxidizing Atmosphere with 4% CO2en_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionacceptedVersionen_US
dc.source.pagenumber587-593en_US
dc.source.journalLight Metalsen_US
dc.identifier.doi10.1007/978-3-030-92529-1_77
dc.identifier.cristin2011769
dc.relation.projectNorges forskningsråd: 237738en_US
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode1


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