Please use this identifier to cite or link to this item: https://physrep.ff.bg.ac.rs/handle/123456789/113
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dc.contributor.authorStojadinović, Stevanen
dc.contributor.authorVasilić, Rastkoen
dc.contributor.authorPetković-Benazzouz, Marijaen
dc.contributor.authorKasalica, Bećkoen
dc.contributor.authorBelča, Ivanen
dc.contributor.authorŽekić, Andrijanaen
dc.contributor.authorZeković, Ljubišaen
dc.date.accessioned2022-06-30T15:20:55Z-
dc.date.available2022-06-30T15:20:55Z-
dc.date.issued2013-01-15en
dc.identifier.issn0169-4332en
dc.identifier.urihttps://physrep.ff.bg.ac.rs/handle/123456789/113-
dc.description.abstractPlasma electrolytic oxidation (PEO) of titanium in sodium metasilicate at 200 mA/cm 2 is investigated using real-time imaging and optical emission spectroscopy. It has been detected that during the PEO process the size of microdischarges becomes larger, while the number of microdischarges is reduced. The species and their ionization states present in PEO microdischarges are identified. The species originate both from titanium anode and from the electrolyte. The spectral line shape analysis of hydrogen Balmer line H β (486.13 nm) indicates the presence of two types of microdischarges during PEO. The discharges are characterized by relatively low electron number densities of N e = 3.8 × 10 15 cm -3 and N e = 4.5 × 10 16 cm -3 . For electron temperature (T e ) measurement we used Ti I lines at 398.18 nm and 501.42 nm and obtained T e in the range of 3700 ± 500 K. Surface coatings formed by PEO process were characterized by AFM, SEM-EDX and XRD. The main elemental components of PEO coatings are Ti, Si and O. The PEO coatings are partly crystallized and mainly composed of anatase, rutile, and amorphous SiO 2 . © 2012 Elsevier B.V. All rights reserved.en
dc.relation.ispartofApplied Surface Scienceen
dc.subjectOptical emission spectroscopyen
dc.subjectPlasma electrolytic oxidation (PEO)en
dc.subjectSodium metasilicateen
dc.subjectTitaniumen
dc.titleCharacterization of the plasma electrolytic oxidation of titanium in sodium metasilicateen
dc.typeArticleen
dc.identifier.doi10.1016/j.apsusc.2012.10.183en
dc.identifier.scopus2-s2.0-84871932844en
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84871932844en
dc.relation.volume265en
dc.relation.firstpage226en
dc.relation.lastpage233en
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
crisitem.author.orcid0000-0002-6589-6296-
crisitem.author.orcid0000-0003-2476-7516-
crisitem.author.orcid0000-0002-8300-6234-
crisitem.author.orcid0000-0001-6124-5333-
crisitem.author.orcid0000-0001-7720-5846-
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