11B MAS NMR spectra of BO3/2-TeO2 glasses
dc.bibliographicCitation.firstPage | 15 | |
dc.bibliographicCitation.journalTitle | Glastechnische Berichte | |
dc.bibliographicCitation.lastPage | 20 | |
dc.bibliographicCitation.volume | 66 | |
dc.contributor.author | Sekiya, Takao | |
dc.contributor.author | Mochida, Norio | |
dc.contributor.author | Ohtsuka, Atsushi | |
dc.contributor.author | Soejima, Ayako | |
dc.contributor.author | Yasumori, Atsuo | |
dc.contributor.author | Yamane, Masayuki | |
dc.date.accessioned | 2024-08-27T15:17:22Z | |
dc.date.available | 2024-08-27T15:17:22Z | |
dc.date.issued | 1993 | |
dc.description.abstract | 11B Magic Angle Spinning Nuclear Magnetic Resonance (MAS NMR) spectra of BO3/2-TeO2 glasses have been used to determine the compositional dependence of the fraction of 4-coordinated boron atoms, N4 = BO4/(BO3+BO4). In 1 BO3/2 ∙ 99 TeO2 (mol%) glass, almost all boron atoms form BO4 tetrahedra. The fraction N4 decreases with increase of BO3/2 content. The authors propose a glass structural model in which the TeO3 trigonal pyramids formed by a part of the tellurium atoms are connected with the BO4 tetrahedra by vertex-sharing. An excess and a deficiency of local charges of a TeO3 trigonal pyramid and a BO4 tetrahedron compensate each other. The conversion of a BO3 triangle to a BO4 tetrahedron is concurrent with the formation of a TeO3 trigonal pyramid. | ger |
dc.description.version | publishedVersion | |
dc.identifier.uri | https://oa.tib.eu/renate/handle/123456789/14967 | |
dc.identifier.uri | https://doi.org/10.34657/13989 | |
dc.language.iso | eng | |
dc.publisher | Offenbach : Verlag der Deutschen Glastechnischen Gesellschaft | |
dc.relation.issn | 0017-1085 | |
dc.rights.license | CC BY 3.0 DE | |
dc.rights.uri | https://creativecommons.org/licenses/by/3.0/de/ | |
dc.subject.ddc | 660 | |
dc.title | 11B MAS NMR spectra of BO3/2-TeO2 glasses | ger |
dc.type | Article | |
dc.type | Text | |
tib.accessRights | openAccess |
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