dc.contributor.author |
Borgheresi M. |
|
dc.contributor.author |
Di Benedetto F. |
|
dc.contributor.author |
Romanelli M. |
|
dc.contributor.author |
Reissner M. |
|
dc.contributor.author |
Lottermoser W. |
|
dc.contributor.author |
Gainov R. |
|
dc.contributor.author |
Khassanov R. |
|
dc.contributor.author |
Tippelt G. |
|
dc.contributor.author |
Giaccherini A. |
|
dc.contributor.author |
Sorace L. |
|
dc.contributor.author |
Montegrossi G. |
|
dc.contributor.author |
Wagner R. |
|
dc.contributor.author |
Amthauer G. |
|
dc.date.accessioned |
2018-04-05T07:09:20Z |
|
dc.date.available |
2018-04-05T07:09:20Z |
|
dc.date.issued |
2017 |
|
dc.identifier.issn |
0342-1791 |
|
dc.identifier.uri |
http://dspace.kpfu.ru/xmlui/handle/net/129667 |
|
dc.description.abstract |
© 2017 Springer-Verlag GmbH Germany The Mössbauer spectra of a nearly stoichiometric natural bornite, Cu 5 FeS 4 , specimen were reinvestigated between 295 and 4.2 K. There is no difference between the Neél temperature T N as determined by the Mössbauer effect or by the susceptibility measurements (T N = 67.5 K). No additional paramagnetic doublet can be observed in the low-temperature MS spectra. The valence state of Fe is Fe (3−x)+ caused by a partial electron transfer from the Cu + ions to the Fe 3+ ions which increases the shielding of the s-electrons by the d-electron density and by this increases the isomer shift to a value intermediate between tetrahedral high-spin Fe 2+ and tetrahedral high-spin Fe 3+ . |
|
dc.relation.ispartofseries |
Physics and Chemistry of Minerals |
|
dc.subject |
Bornite |
|
dc.subject |
Chemical bond in sulphides |
|
dc.subject |
Magnetic properties |
|
dc.subject |
Mössbauer spectroscopy |
|
dc.title |
Mössbauer study of bornite and chemical bonding in Fe-bearing sulphides |
|
dc.type |
Article in Press |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1 |
|
dc.source.id |
SCOPUS03421791-2017-SID85024494773 |
|