Characterisation of Ni carbonate-bearing minerals by UV-Vis-NIR spectroscopy

被引:10
|
作者
Reddy, B. Jagannadha [1 ]
Keeffe, Eloise C. [1 ]
Frost, Ray L. [1 ]
机构
[1] Queensland Univ Technol, Inorgan Mat Res Program, Sch Phys & Chem Sci, Brisbane, Qld 4001, Australia
关键词
NEAR-INFRARED SPECTROSCOPY; NATURAL HYDROTALCITES CARRBOYDITE; ROSASITE GROUP; RAMAN-SPECTROSCOPY; ABSORPTION-SPECTRA; CRYSTAL-STRUCTURES; TAKOVITE; NICKEL; MALACHITE; HYDROHONESSITE;
D O I
10.1007/s11243-009-9324-7
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four nickel carbonate-bearing minerals from Australia have been investigated to study the effect of Ni for Mg substitution. The spectra of nullaginite, zaratite, widgiemoolthalite and takovite show three main features in the range of 26,720-25,855 cm(-1) (nu(1)-band), 15,230-14,740 cm(-1) (nu(2)-band) and 9,200-9,145 cm(-1) (nu(3)-band) which are characteristic of divalent nickel in six-fold coordination. The Crystal Field Stabilization Energy (CFSE) of Ni2+ in the four carbonates is calculated from the observed (3)A(2g)(F-3) -> T-3(2g)(F-3) transition. CFSE is dependent on mineralogy, crystallinity and chemical composition (Al/Mg-content). The splitting of the nu(1)- and nu(3)-bands and non-Gaussian shape of nu(3)-band in the minerals are the effects of Ni-site distortion from regular octahedral. The effect of structural cation substitutions (Mg2+, Ni2+, Fe2+ and trivalent cations, Al3+, Fe3+) in the carbonate minerals is noticed on band shifts. Thus, electronic bands in the UV-Vis-NIR spectra and the overtones and combination bands of OH and carbonate ion in NIR show shifts to higher wavenumbers, particularly for widgiemoolthalite and takovite.
引用
收藏
页码:279 / 287
页数:9
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