The crystal chemistry and crystal structure of the rare earth element phosphates, monazite-(Ce), Ce(PO4), and xenotime-(Y), Y(PO4), as well as the arsenates, gasparite-(Ce), Ce(AsO4), and chernovite-(Y), Y(AsO4), from the hydrothermal quartz-bearing fissures, related to pegmatites overprinted by amphibolite facies, cropping out at Mt. Cervandone, Western Alps, Piedmont, Italy, have been investigated by means of electron microprobe analysis in wavelength dispersion mode and single-crystal X-ray diffraction. The chemical data reveal the occurrence of a full solid solution among the isostructural chernovite-(Y) and xenotime-(Y) with tetragonal symmetry, whereas a wide miscibility gap is observed for the isostructural gasparite-(Ce) and monazite-(Ce) of Mt. Cervandone, with monoclinic symmetry. A significant chemical heterogeneity has been observed for several investigated samples, especially related to the Th content, which is locally enriched in ThSiO4 grains. The analysis of the refined structural models demonstrates the significant control played by the composition of the tetrahedrally-coordinated (As,P)-bearing sites on the bulk unit-cell volume, and on the size and shape of the (REE)-coordination polyhedra.

Crystal chemistry and miscibility of chernovite-(Y), xenotime-(Y), gasparite-(Ce) and monazite-(Ce) from Mt. Cervandone (Western Alps, Italy) / F. Pagliaro, P. Lotti, A. Guastoni, N. Rotiroti, T. Battiston, G. Diego Gatta. - In: MINERALOGICAL MAGAZINE. - ISSN 0026-461X. - 86:1(2022 Feb), pp. 150-167. [10.1180/mgm.2022.5]

Crystal chemistry and miscibility of chernovite-(Y), xenotime-(Y), gasparite-(Ce) and monazite-(Ce) from Mt. Cervandone (Western Alps, Italy)

F. Pagliaro
Primo
Writing – Review & Editing
;
P. Lotti
Secondo
Writing – Original Draft Preparation
;
N. Rotiroti
Membro del Collaboration Group
;
T. Battiston
Penultimo
Membro del Collaboration Group
;
G. Diego Gatta
Ultimo
Supervision
2022

Abstract

The crystal chemistry and crystal structure of the rare earth element phosphates, monazite-(Ce), Ce(PO4), and xenotime-(Y), Y(PO4), as well as the arsenates, gasparite-(Ce), Ce(AsO4), and chernovite-(Y), Y(AsO4), from the hydrothermal quartz-bearing fissures, related to pegmatites overprinted by amphibolite facies, cropping out at Mt. Cervandone, Western Alps, Piedmont, Italy, have been investigated by means of electron microprobe analysis in wavelength dispersion mode and single-crystal X-ray diffraction. The chemical data reveal the occurrence of a full solid solution among the isostructural chernovite-(Y) and xenotime-(Y) with tetragonal symmetry, whereas a wide miscibility gap is observed for the isostructural gasparite-(Ce) and monazite-(Ce) of Mt. Cervandone, with monoclinic symmetry. A significant chemical heterogeneity has been observed for several investigated samples, especially related to the Th content, which is locally enriched in ThSiO4 grains. The analysis of the refined structural models demonstrates the significant control played by the composition of the tetrahedrally-coordinated (As,P)-bearing sites on the bulk unit-cell volume, and on the size and shape of the (REE)-coordination polyhedra.
monazite; xenotime; chernovite; gasparite; rare earth elements; crystal chemistry; crystal structure; solid solution; X-ray diffraction
Settore GEO/09 - Georisorse Miner.Appl.Mineral.-Petrogr.per l'amb.e i Beni Cul
feb-2022
19-gen-2022
https://www.cambridge.org/core/journals/mineralogical-magazine/article/crystal-chemistry-and-miscibility-of-chernovitey-xenotimey-gasparitece-and-monazitece-from-mt-cervandone-western-alps-italy/B1E3DCA83E8A48F6FCB4BE3D02E1E203
Article (author)
File in questo prodotto:
File Dimensione Formato  
Pagliaro_REE_minerals_Cervandone_MinMag.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 1.67 MB
Formato Adobe PDF
1.67 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/903520
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 0
social impact