print Print
Please select which sections you would like to print:
verifiedCite
While every effort has been made to follow citation style rules, there may be some discrepancies. Please refer to the appropriate style manual or other sources if you have any questions.
Select Citation Style
Feedback
Corrections? Updates? Omissions? Let us know if you have suggestions to improve this article (requires login).
Thank you for your feedback

Our editors will review what you’ve submitted and determine whether to revise the article.

This class is composed of a large number of minerals, but relatively few are common. All contain anionic (SO4)2– groups in their structures. These anionic complexes are formed through the tight bonding of a central S6+ ion to four neighbouring oxygen atoms in a tetrahedral arrangement around the sulfur. This closely knit group is incapable of sharing any of its oxygen atoms with other SO4 groups; as such, the tetrahedrons occur as individual, unlinked groups in sulfate mineral structures.

Common sulfates
Source: Modified from C. Klein and C.S. Hurlbut, Jr.,
Manual of Mineralogy, copyright © 1985 John Wiley
and Sons, Inc., reprinted with permission of John Wiley
and Sons.
barite group
barite BaSO4
celestite SrSO4
anglesite PbSO4
anhydrite CaSO4
gypsum CaSO4 · 2H2O

Members of the barite group constitute the most important and common anhydrous sulfates. They have orthorhombic symmetry with large divalent cations bonded to the sulfate ion. In barite (BaSO4), each barium ion is surrounded by 12 closest oxygen ions belonging to seven distinct SO4 groups. Anhydrite (CaSO4) exhibits a structure very different from that of barite since the ionic radius of Ca2+ is considerably smaller than Ba2+. Each calcium cation can only fit eight oxygen atoms around it from neighbouring SO4 groups. Gypsum (CaSO4 ∙ 2H2O) is the most important and abundant hydrous sulfate.