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Electronic and vibrational spectra of gaspeite

Reddy, B. Jagannadha & Frost, Ray L. (2004) Electronic and vibrational spectra of gaspeite. Neues Jahrbuch fuer Mineralogie. Monatshefte, 2004(11), pp. 525-536.

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Abstract

Visible, near-infrared, IR and Raman spectra of magnesian gaspeite are presented. Nickel ion is the main source of the electronic bands as it is the principal component in the mineral where as the bands in IR and Raman spectra are due to the vibrational processes in the carbonate ion as an entity. The combination of electronic absorption and vibrational spectra (including near-infrared, FTIR and Raman) of magnesian gaspeite are explained in terms of the cation co-ordination and the behaviour of CO32– anion in the Ni–Mg carbonate. The electronic absorption spectrum consists of three broad and intense bands at 8130, 13160 and 22730 cm–1 due to spin-allowed transitions and two weak bands at 20410 and 30300 cm–1 are assigned to spin-forbidden transitions of Ni2+ in an octahedral symmetry. The crystal field parameters evaluated from the observed bands are Dq = 810; B = 800 and C = 3200 cm–1. The two bands in the near-infrared spectrum at 4330 and 5130 cm–1 are overtone and combination of CO32– vibrational modes. For the carbonate group, infrared bands are observed at 1020 cm–1(1 ), 870 cm–1 (2), 1418 cm–1 (3) and 750 cm–1 (4), of which3, the asymmetric stretching mode is most intense. Three well resolved Raman bands at 1571, 1088 and 331 cm–1 are assigned to 3, 1 and MO stretching vibrations.

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11 citations in Web of Science®

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ID Code: 23214
Item Type: Journal Article
DOI: 10.1127/0028-3649/2004/2004-0525
ISSN: 0028-3649
Divisions: Past > QUT Faculties & Divisions > Faculty of Science and Technology
Copyright Owner: Copyright 2004 E. Schweizerbartsche Verlagsbuchhandlung
Deposited On: 17 Jun 2009 23:45
Last Modified: 07 Mar 2012 01:25

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