We compare two different approaches to fitting the Fe-57 M6ssbauer spectra of paramagnetic state minerals: the widespread practice of using Lorentzian line doublets with adjustable F widths and a new method (Rancourt and Ping, 1991) based on quadrupole splitting distributions (QSDs). We argue that t
Mössbauer spectroscopy of minerals
✍ Scribed by D. G. Rancourt
- Publisher
- Springer-Verlag
- Year
- 1994
- Tongue
- English
- Weight
- 679 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0342-1791
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✦ Synopsis
We demonstrate by trade-off and error analysis of representative spectra that paramagnetic state M6ssbauer spectroscopy of 2:1 layer silicates cannot resolve the octahedral Fe 2+ cis (M2) and trans (M1) sites. We show that it is impossible to extract cis/trans population ratios from two Fe 2+ doublet analyses of the spectra and that, instead, one has a single continuous Fe 2+ quadrupole splitting distribution (QSD) that cannot reliably or uniquely be partitioned into its constituents. Whereas extracted cis/trans ratios do not contribute to evaluating site occupancies, the QSDs themselves in principle contain much local structural and chemical information that should be the focus of futur work.
📜 SIMILAR VOLUMES
We develop the methodology of quadrupole splitting distribution (QSD) analysis by evaluating the influences of absorber thickness, absorber texture, and the asumed Lorentzian width on the extracted QSD. We then present the first study to describe the M6ssbauer spectra of members of a mineral family