z-logo
Premium
Raman spectroscopic study of the mineral gerstleyite Na 2 (Sb,As) 8 S 13 ·2H 2 O and comparison with some heavy‐metal sulfides
Author(s) -
Frost Ray L.,
Bahfenne Silmarilly,
Keeffe Eloise C.
Publication year - 2010
Publication title -
journal of raman spectroscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.748
H-Index - 110
eISSN - 1097-4555
pISSN - 0377-0486
DOI - 10.1002/jrs.2627
Subject(s) - stibnite , raman spectroscopy , chemistry , antimony , realgar , analytical chemistry (journal) , cinnabar , sulfide , mineralogy , inorganic chemistry , sphalerite , optics , physics , pyrite , hematite , organic chemistry , chromatography
The mineral gerstleyite is described as a sulfosalt as opposed to a sulfide. This study focuses on the Raman spectrum of gerstleyite Na 2 (Sb,As) 8 S 13 ·2H 2 O and makes a comparison with the Raman spectra of other common sulfides including stibnite, cinnabar and realgar. The intense Raman bands of gerstleyite at 286 and 308 cm −1 are assigned to the SbS 3 E antisymmetric and A 1 symmetric stretching modes of the SbS 3 units. The band at 251 cm −1 is assigned to the bending mode of the SbS 3 units. The mineral stibnite also has basic structural units of Sb 2 S 3 and SbS 3 pyramids with C 3 v symmetry. Raman bands of stibnite Sb 2 S 3 at 250, 296, 372 and 448 cm −1 are assigned to SbS stretching vibrations and the bands at 145 and 188 cm −1 to SSbS bending modes. The Raman band for cinnabar HgS at 253 cm −1 fits well with the assignment of the band for gerstleyite at 251 cm −1 to the SSbS bending mode. Raman bands in similar positions are observed for realgar AsS and orpiment As 2 S 3 . Copyright © 2010 John Wiley & Sons, Ltd.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom