Authentication of the AR-51 stony meteorite with physical techniques for characterization

Descripción del Articulo

There is evidence for the authentication of the meteoritic sample Ar-51 as a stone meteorite, found in the Arequipa Region, Peru. The analytical techniques used for this study were X-ray fluorescence (XRF), X-ray diractometry (XRD) and room temperature (RT) transmission Mössbauer spectroscopy (TMS),...

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Detalles Bibliográficos
Autores: Cerón, María, Bravo, Jorge
Formato: artículo
Fecha de Publicación:2021
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/20320
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/fisica/article/view/20320
Nivel de acceso:acceso abierto
Materia:Ar-51 meteorite
transmission Mössbauer spectroscopy
X-ray difractometry
X-ray fluorescence
albite
pyroxene
magnetite
maghemite
Meteorito Ar-51
espectroscopia Mössbauer de transmisión
difractometría de rayos X
fluorescencia de rayos X
albita
piroxeno
magnetita
maghemita
Descripción
Sumario:There is evidence for the authentication of the meteoritic sample Ar-51 as a stone meteorite, found in the Arequipa Region, Peru. The analytical techniques used for this study were X-ray fluorescence (XRF), X-ray diractometry (XRD) and room temperature (RT) transmission Mössbauer spectroscopy (TMS), The results pertaining the structural phases found by XRD include mainly albite, pyroxene, clinopyroxene, augite, maghemite and magnetite. TMS reveals that its mineralogical composition includes three magnetic sextets and two paramagnetic doublets. Two of the sextets are assigned to cation sites in magnetite: the sextet with the higher hyperne magnetic eld is assigned to an Fe3+ cation A site (tetrahedral position) and the second one is assigned to the B site, which is occupied evenly by Fe3+ and Fe2+ cations (octahedral position); and the third magnetic sextet is assigned to maghemite. The presence of both sites (octahedral and tetrahedral layers) along the (111) direction induces plane superposition which is considered more stable. Two of the paramagnetic doublets are associated with structural Fe2+ cations that could be assigned to subgroups of the pyroxene silicates, and the third doublet is associated to a Fe3+ cation site.
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