2007
DOI: 10.1007/s10751-008-9646-4
|View full text |Cite
|
Sign up to set email alerts
|

Determination of quadrupole splitting for 57Fe in M1 and M2 sites of both olivine and pyroxene in ordinary chondrites using Mössbauer spectroscopy with high velocity resolution

Abstract: Study of 11 ordinary chondrites using Mössbauer spectroscopy with high velocity resolution revealed two crystallographically non-equivalent octahedral sites M1 and M2 in subspectra of olivine and pyroxene which were observed previously in pure natural or synthetic silicates only. Mössbauer hyperfine parameters related to M1 and M2 sites in olivine and pyroxene determined from Mössbauer spectra of ordinary chondrites were analyzed and compared with parameters of pure natural and synthetic silicates.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
4
0

Year Published

2010
2010
2022
2022

Publication Types

Select...
6
2
1

Relationship

2
7

Authors

Journals

citations
Cited by 17 publications
(5 citation statements)
references
References 16 publications
1
4
0
Order By: Relevance
“…4 ) show an asymmetric quadrupole doublet which can be fitted by using at least three independent spectral components. Comparing the experimental values of isomer shift, IS, and quadrupole splitting, QS (Table 1 ), with those reported in the literature [ 28 – 32 ], it is easy to attribute the two doublets with high intensities (red and blue lines in Fig. 3 ) to Fe 2+ located at M1 and M2 sites, respectively, confirming that also in this case, there is no cationic site preference for the iron ions.…”
Section: Resultssupporting
confidence: 80%
“…4 ) show an asymmetric quadrupole doublet which can be fitted by using at least three independent spectral components. Comparing the experimental values of isomer shift, IS, and quadrupole splitting, QS (Table 1 ), with those reported in the literature [ 28 – 32 ], it is easy to attribute the two doublets with high intensities (red and blue lines in Fig. 3 ) to Fe 2+ located at M1 and M2 sites, respectively, confirming that also in this case, there is no cationic site preference for the iron ions.…”
Section: Resultssupporting
confidence: 80%
“…The first studies of H and L ordinary chondrites using Mössbauer spectroscopy with a high velocity resolution were done in [75][76][77][78]. These results demonstrated the possibility to distinguish spectral components related to the M1 and M2 sites in olivine and orthopyroxene.…”
Section: H Ordinary Chondritesmentioning
confidence: 90%
“…It should be noted that the authors of [93,94] used the full static Hamiltonian to fit troilite component. Applications of Mössbauer spectroscopy with a high velocity resolution, as mentioned in the previous section, permitted to distinguish spectral components related to the 57 Fe in crystallographically non-equivalent M1 and M2 sites in silicate crystals as well as to the minor iron-bearing phases [75][76][77][78][79][80][81][82][83][84]. The difference between the Mössbauer spectra of L ordinary chondrites Mbale L5/6, Mount Tazerzait L5, and Saratov L4 measured with a low and high velocity resolution can be illustrated in Figure 26.…”
Section: Ordinary Chondritesmentioning
confidence: 98%
“…4. Based on our previous data for olivine study [4][5][6][11][12][13], we related the component 1 with the larger ǻE Q and S values to 57 Fe in the M1 sites while the component 2 with the smaller ǻE Q and S values was related to 57 Fe in the M2 sites in olivine. The component 3 had parameters which we cannot relate to any impurity.…”
Section: Mössbauer Spectroscopymentioning
confidence: 98%