Redox chemistry of iron-manganese and iron-chromium interactions in soda-lime-silica glass melts

dc.bibliographicCitation.firstPage1
dc.bibliographicCitation.journalTitleGlass Science and Technologyeng
dc.bibliographicCitation.lastPage5
dc.bibliographicCitation.volume71
dc.contributor.authorNölle, Günther
dc.date.accessioned2024-01-08T07:36:13Z
dc.date.available2024-01-08T07:36:13Z
dc.date.issued1998
dc.description.abstractGlass melts are mostly not in a chemical equilibrium with a coexisting gas phase, it does not adjust before maintaining the melt at a constant temperature and a constant gas phase for hours. But the one-phase equilibrium between several polyvalent Clements in a melt above the glass transition temperature always exists, it adjusts spontaneously. Below the transition temperature the redox State is invariably frozen-in. The calculation of redox states must be based on the matter and Charge balance (stoichiometric equations) and equilibrium relations (mass-action law). Such a calculation of Schreiber's experimental results was consistently possible. Accordingly cooled glasses are free from Cr⁶⁺, if the glass contains Fe²⁺. To achieve this one has to melt oxidized chromium-containing glasses with sufficient iron content.eng
dc.description.versionpublishedVersion
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/14156
dc.identifier.urihttps://doi.org/10.34657/13186
dc.language.isoeng
dc.publisherOffenbach : Verlag der Deutschen Glastechnischen Gesellschaft
dc.relation.issn0946-7475
dc.rights.licenseCC BY 3.0 DE
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/de/
dc.subject.ddc660
dc.titleRedox chemistry of iron-manganese and iron-chromium interactions in soda-lime-silica glass meltseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
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