Sulfate Mineral
sulfate mineral, sulfate also spelled Sulphate, any naturally occurring salt of sulfuric acid. About 200 distinct kinds of sulfates are recorded in mineralogical literature, but most of them are of rare and local occurrence. Abundant deposits of sulfate minerals, such as barite and celestite, are exploited for the preparation of metal salts. Many beds of sulfate minerals are mined for fertilizer and salt preparations, and beds of pure gypsum are mined for the preparation of plaster of paris.
 
name
 
colour
 
lustre
 
Mohs hardness
 
specific gravity
 
 
alum
 
colourless; white
 
vitreous
 
2–2½
 
1.8
 
 
alunite
 
white; grayish, yellowish, reddish, reddish brown
 
vitreous
 
3½–4
 
2.6–2.9
 
 
alunogen
 
white; yellowish or reddish
 
vitreous to silky
 
1½–2
 
1.8
 
 
anglesite
 
colourless to white; often tinted gray, yellow, green, or blue
 
adamantine to resinous or vitreous
 
2½–3
 
6.4
 
 
anhydrite
 
colourless to bluish or violet
 
vitreous to pearly
 
3½
 
3.0
 
 
antlerite
 
emerald to blackish green; light green
 
vitreous
 
3½
 
3.9
 
 
barite
 
colourless to white; also variable
 
vitreous to resinous
 
3–3½
 
4.5
 
 
botryogen
 
light to dark orange red
 
vitreous
 
2–2½
 
2.1
 
 
brochantite
 
emerald to blackish green; light green
 
vitreous
 
3½–4
 
4.0
 
 
caledonite
 
deep verdigris green or bluish green
 
resinous
 
2½–3
 
5.8
 
 
celestite
 
pale blue; white, reddish, greenish, brownish
 
vitreous
 
3–3½
 
4.0
 
 
chalcanthite
 
various shades of blue
 
vitreous
 
2½
 
2.3
 
 
coquimbite
 
pale violet to deep purple
 
vitreous
 
2½
 
2.1
 
 
epsomite
 
colourless; aggregates are white
 
vitreous; silky to earthy (fibrous)
 
2–2½
 
1.7
 
 
glauberite
 
gray; yellowish
 
vitreous to slightly waxy
 
2½–3
 
2.75–2.85
 
 
gypsum
 
colourless; white, gray, brownish, yellowish (massive)
 
subvitreous
 
2 (a hardness standard)
 
2.3
 
 
halotrichite
 
colourless to white
 
vitreous
 
1.5
 
1.7 (pick) to 1.9 (halo)
 
 
jarosite
 
ochre yellow to dark brown
 
subadamantine to vitreous; resinous on fracture
 
2½–3½
 
2.9–3.3
 
 
kainite
 
colourless; gray, blue, violet, yellowish, reddish
 
vitreous
 
2½–3
 
2.2
 
 
kieserite
 
colourless; grayish white, yellowish
 
vitreous
 
3.5
 
2.6
 
 
linarite
 
deep azure blue
 
vitreous to subadamantine
 
2.5
 
5.3
 
 
mirabilite
 
colourless to white
 
vitreous
 
1½–2
 
1.5
 
 
plumbojarosite
 
golden brown to dark brown
 
dull to glistening or silky
 
soft
 
3.7
 
 
polyhalite
 
colourless; white or gray; often salmon pink from included iron oxide
 
vitreous to resinous
 
3.5
 
2.8
 
 
thenardite
 
colourless; reddish, grayish, yellowish, or yellow brown
 
vitreous to resinous
 
2½–3
 
2.7
 
 
name
 
habit
 
fracture or cleavage
 
refractive indices
 
crystal system
 
 
alum
 
columnar or granular massive
 
conchoidal fracture
 
n = 1.453–1.466
 
isometric
 
 
alunite
 
granular to dense massive
 
conchoidal fracture
 
omega = 1.572 
epsilon = 1.592
hexagonal
 
 
alunogen
 
fibrous masses and crusts
 
one perfect cleavage
 
alpha = 1.459–1.475 
beta = 1.461–1.478
gamma = 1.884–1.931
triclinic
 
 
anglesite
 
granular to compact massive; tabular or prismatic crystals
 
one good, one distinct cleavage
 
alpha = 1.868–1.913 
beta = 1.873–1.918
gamma = 1.884–1.931
orthorhombic
 
 
anhydrite
 
granular or fibrous massive; concretionary (tripestone)
 
two perfect, one good cleavage
 
alpha = 1.567–1.580 
beta = 1.572–1.586
gamma = 1.610–1.625
orthorhombic
 
 
antlerite
 
thick tabular crystals
 
one perfect cleavage
 
alpha = 1.726 
beta = 1.738
gamma = 1.789
orthorhombic
 
 
barite
 
usually in tabular crystals; rosettes (desert roses); massive
 
one perfect, one good cleavage
 
alpha = 1.633–1.648 
beta = 1.634–1.649
gamma = 1.645–1.661
orthorhombic
 
 
botryogen
 
reniform, botryoidal, or globular aggregates
 
one perfect, one good cleavage
 
alpha = 1.523 
beta = 1.530
gamma = 1.582
monoclinic
 
 
brochantite
 
prismatic to hairlike crystal and crystal aggregates; granular massive; crusts
 
one perfect cleavage
 
alpha = 1.728 
beta = 1.771
gamma = 1.800
monoclinic
 
 
caledonite
 
coating of small elongated crystals
 
one perfect cleavage
 
alpha = 1.815–1.821 
beta = 1.863–1.869
gamma = 1.906–1.912
orthorhombic
 
 
celestite
 
tabular crystals; fibrous massive
 
one perfect, one good cleavage
 
alpha = 1.618–1.632 
beta = 1.620–1.634
gamma = 1.627–1.642
orthorhombic
 
 
chalcanthite
 
short prismatic crystals; granular masses; stalactites and reniform masses
 
conchoidal fracture
 
alpha = 1.514 
beta = 1.537
gamma = 1.543
triclinic
 
 
coquimbite
 
prismatic and pyramidal crystals; granular massive
 
 
omega = 1.536 
epsilon = 1.572
hexagonal
 
 
epsomite
 
fibrous or hairlike crusts; woolly efflorescences
 
one perfect cleavage
 
alpha = 1.430–1.440 
beta = 1.452–1.462
gamma = 1.457–1.469
orthorhombic
 
 
glauberite
 
tabular, dipyramidal, or prismatic crystals
 
one perfect cleavage
 
alpha = 1.515 
beta = 1.535
gamma = 1.536
monoclinic
 
 
gypsum
 
elongated tabular crystals (some 5 ft long; others twisted or bent); granular or fibrous masses; rosettes
 
one perfect cleavage
 
alpha = 1.515–1.523 
beta = 1.516–1.526
gamma = 1.524–1.532
monoclinic
 
 
halotrichite
 
aggregates of hairlike crystals
 
conchoidal fracture
 
alpha = 1.475–1.480 
beta = 1.480–1.486
gamma = 1.483–1.490
monoclinic
 
 
jarosite
 
minute crystals; crusts; granular or fibrous massive
 
one distinct cleavage
 
omega = 1.82 
epsilon = 1.715
hexagonal
 
 
kainite
 
granular massive; crystalline coatings
 
one perfect cleavage
 
alpha = 1.494 
beta = 1.505
gamma = 1.516
monoclinic
 
 
kieserite
 
granular massive, intergrown with other salts
 
two perfect cleavages
 
alpha = 1.520 
beta = 1.533
gamma = 1.584
monoclinic
 
 
linarite
 
elongated tabular crystals, either singly or in groups
 
one perfect cleavage; conchoidal fracture
 
alpha = 1.809 
beta = 1.839
gamma = 1.859
monoclinic
 
 
mirabilite
 
short prisms; lathlike or tabular crystals; crusts or fibrous masses; granular massive
 
one perfect cleavage
 
alpha = 1.391–1.397 
beta = 1.393–1.410
gamma = 1.395–1.411
monoclinic
 
 
plumbojarosite
 
crusts, lumps, compact masses of microscopic hexagonal plates
 
one fair cleavage
 
omega = 1.875 
epsilon = 1.786
hexagonal
 
 
polyhalite
 
fibrous to foliated massive
 
one perfect cleavage
 
alpha = 1.547 
beta = 1.560
gamma = 1.567
triclinic
 
 
thenardite
 
rather large crystals; crusts, efflorescences
 
one perfect, one fair cleavage
 
alpha = 1.464–1.471 
beta = 1.473–1.477
gamma = 1.481–1.485
orthorhombic
 
All sulfates possess an atomic structure based on discrete insular sulfate (SO42-) tetrahedra, i.e., ions in which four oxygen atoms are symmetrically distributed at the corners of a tetrahedron with the sulfur atom in the centre. These tetrahedral groups do not polymerize, and the sulfate group behaves as a single negatively charged molecule, or complex. Thus, sulfates are distinct from the silicates and borates, which link together into chains, rings, sheets, or frameworks.
Sulfate minerals can be found in at least four kinds: as late oxidation products of preexisting sulfide ores, as evaporite deposits, in circulatory solutions, and in deposits formed by hot water or volcanic gases. Many sulfate minerals occur as basic hydrates of iron, cobalt, nickel, zinc, and copper at or near the source of preexisting primary sulfides. The sulfide minerals, through exposure to weathering and circulating water, have undergone oxidation in which the sulfide ion is converted to sulfate and the metal ion also is changed to some higher valence state. Noteworthy beds of such oxidation products occur in desert regions, such as Chuquicamata, Chile, where brightly coloured basic copper and ferric iron sulfates have accumulated. The sulfate anions generated by oxidation processes may also react with calcium carbonate rocks to form gypsum, CaSO4·2H2O. Sulfates formed by the oxidation of primary sulfides include antlerite [Cu3(SO4)(OH)4], brochantite [Cu4(SO4)(OH)6], chalcanthite [Cu2+(SO4)·5Η2Ο], anglesite (PbSO4), and plumbojarosite [PbFe3+6(SO4)4(OH)12].
Soluble alkali and alkaline-earth sulfates crystallize upon evaporation of sulfate-rich brines and trapped oceanic salt solutions. Such brines can form economically important deposits of sulfate, halide, and borate minerals in thick parallel beds, as the potash deposits at Stassfurt, Ger., and the southwestern United States. Many of the sulfate minerals are salts of more than one metal, such as polyhalite, which is a combination of potassium, calcium, and magnesium sulfates.
Sulfate minerals common in evaporite deposits include anhydrite, gypsum, thenardite (Na2SO4), epsomite (MgSO4·7H2O), glauberite [Na2Ca(SO4)2], kainite (MgSO4·KCl·3H2O), kieserite (MgSO4·H2O), mirabilite (Na2SO4·10H2O), and polyhalite [K2Ca2Mg(SO4)4·2H2O].
Groundwater carrying sulfate anions reacts with calcium ions in muds, clays, and limestones to form beds of gypsum. The massive material is called alabaster or plaster of paris (originally found in the clays and muds of the Paris basin). If such beds become deeply buried or metamorphosed (altered by heat and pressure), anhydrite may form by dehydration of the gypsum.
Numerous sulfates, usually simple, are formed directly from hot aqueous solutions associated with fumarolic (volcanic gas) vents and late-stage fissure systems in ore deposits. Noteworthy examples include anhydrite, barite, and celestine.
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