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The parisite–(Ce) enigma: challenges in the identification of fluorcarbonate minerals

Manuela Zeug; Lutz Nasdala; Martin Ende; Gerlinde Habler; Christoph Hauzenberger; Chutimun Chanmuang N.; Radek Škoda; Dan Topa; Manfred Wildner; Richard Wirth
Mineralogy and Petrology · Vol. 115, Issue 1 · pp. 1-19 · 2021

Abstract

A multi-methodological study was conducted in order to provide further insight into the structural and compositional complexity of rare earth element (REE) fluorcarbonates, with particular attention to their correct assignment to a mineral species. Polycrystals from La Pita Mine, Municipality de Maripí, Boyacá Department, Colombia, show syntaxic intergrowth of parisite–(Ce) with röntgenite–(Ce) and a phase which is assigned to B 3 S 4 (i.e., bastnäsite-3–synchisite-4; still unnamed) fluorcarbonate. Transmission electron microscope (TEM) images reveal well-ordered stacking patterns of two monoclinic polytypes of parisite–(Ce) as well as heavily disordered layer sequences with varying lattice fringe spacings. The crystal structure refinement from single crystal X-ray diffraction data – impeded by twinning, complex stacking patterns, sequential and compositional faults – indicates that the dominant parisite–(Ce) polytype M 1 has space group Cc . Parisite–(Ce), the B 3 S 4 phase and röntgenite–(Ce) show different BSE intensities from high to low. Raman spectroscopic analyses of parisite–(Ce), the B 3 S 4 phase and röntgenite–(Ce) reveal different intensity ratios of the three symmetric CO 3 stretching bands at around 1100 cm −1 . We propose to non-destructively differentiate parisite–(Ce) and röntgenite–(Ce) by their 1092 cm −1 / 1081 cm −1 ν 1 (CO 3 ) band height ratio.

Bibliographic Information

JournalMineralogy and Petrology
PublisherSpringer
Publication Date2021-02-01
Publication Year2021
Volume115
Issue1
Pages1-19
Document TypeJournal Article
Print ISSN0930-0708
eISSN1438-1168
DOI10.1007/s00710-020-00723-x

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NARA Access Coverage1948-01-01~Current
Journal Homepagehttps://www.springer.com/journal/710
Publisher PageOpen Publisher Page
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