Minerals associated with economically recoverable metals Elemental forms Sulfides Oxides Carbonates Sulfate salt Elemental copper Chalcocite, Cu 2 SChalcanthite,

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Minerals associated with economically recoverable metals Elemental forms Sulfides Oxides Carbonates Sulfate salt Elemental copper Chalcocite, Cu 2 SChalcanthite, CuSO 4 *5H 2 O Malachite, Cu 2 CO 3 (OH) 2 Cuprite, Cu 2 O

Wand, nicknamed ‘Fat Albert’ contains 2 electrodes and a thermistor

Voltammetry at 7,500 ft depth Black Smoker chemistry – Scans up to 220º C  lots of Fe 2+, HS -, FeS (aq), tens to hundreds of millimolar Fe and S Riftia field chemistry – Scans up to 20º C  little/no Fe 2+, FeS (aq), few mM HS -,

Sulfides Part 1 Substitution into sulfides is very common As and Se substitute for S very easily Au can substitute in cation sites (auriferrous minerals) Different metals swap in and out pretty easily  Cu and Fe for instance have a wide range of solid solution materials

Sulfide Minerals Minerals with S - or S 2- (monosulfides) or S 2 2- (disulfides) as anionic group Transition metals bonded with sulfide anion groups

Iron Sulfides Mackinawite – FeS Greigite – Fe x S y Pyrite – FeS 2 (cubic) Marcasite – FeS 2 (orthorhombic) Troilite – FeS end member Pyrrhotite – Fe 1-x S (slightly deficient in iron) Arsenopyrite – FeAsS Chalcopyrite – CuFeS 2

Other important sulfides Galena – PbS Sphalerite/wurtzite – ZnS Cinnabar – HgS Molybdenite – MoS Covellite – CuS Chalcocite – Cu 2 S Acanthite or Argenite – AgS Stibnite – Sb 2 S 3 Orpiment – As 2 S 3 ; Realgar – AsS

Sulfides are reduced minerals  what happens when they contact O 2 ? This is the basis for supergene enrichment and acidic mine drainage

Actively Oxidizing Pyrite FeS O 2 + H 2 O  Fe SO H + FeS Fe H 2 O  15 Fe SO H + 14Fe O H +  14 Fe H 2 O Sulfur species and H + generation: –FeS Fe 3+  3 Fe 2+ + ¼ S H + –FeS Fe H 2 O  8 Fe S 4 O H +

AMD neutralization Metals are soluble in low pH solutions – can get 100’s of grams of metal into a liter of very acidic solution HOWEVER – eventually that solution will get neutralized (reaction with other rocks, CO 2 in the atmosphere, etc.) and the metals are not so soluble  but oxidized S (sulfate, SO 4 2- ) is very soluble A different kind of mineral is formed!

Ely Mine

Oxides - Oxyhydroxides FeOOH minerals  Goethite or Limonite (FeOOH)  important alteration products of weathering Fe-bearing minerals Hematite (Fe 2 O 3 )  primary iron oxide in Banded Iron Formations Boehmite (AlOOH)  primary mineral in bauxite ores (principle Al ore) which forms in tropical soils Gibbsite (Al(OH) 3 ) – common Al oxide forming in aqueous sysems Mn oxides  form Mn nodules in the oceans (estimated they cover 10-30% of the deep Pacific floor) Many other oxides important in metamorphic rocks…

Al oxides Aluminum occurs in economic deposits principally as bauxite Bauxite is a mixture of Al oxides and oxyhydroxides: – Diaspore - AlO(OH) – Gibbsite - Al(OH)3 – Böhmite - AlO(OH) Al is a residual phase and bauxite occurs where weathering is extreme and thick layers of aluminum oxyhydroxide are left over

Mn oxides - oxyhydroxides Mn exists as 2+, 3+, and 4+; oxide minerals are varied, complex, and hard to ID – ‘Wad’  soft (i.e. blackens your fingers), brown-black fine- grained Mn oxides – ‘Psilomelane’  hard (does not blacked fingers) gray-black botroyoidal, massive Mn oxides XRD analyses do not easily distinguish different minerals, must combine with TEM, SEM, IR spectroscopy, and microprobe work

Romanechite Ba.66 (Mn 4+,Mn 3+ ) 5 O 10 *1.34H 2 O  Psilomelane Pyrolusite MnO2 Ramsdellite MnO2 Nsutite Mn(O,OH)2 Hollandite Bax(Mn4+,Mn3+)8O16 Cryptomelane Kx(Mn4+,Mn3+)8O16 Manjiroite Nax(Mn4+,Mn3+)8O16 Coronadite Pbx(Mn4+,Mn3+)8O16 Todorokite (Ca,Na,K)X(Mn4+,Mn3+)6O12*3.5H2O Lithiophorite LiAl2(Mn2+Mn3+)O6(OH)6 Chalcophanite ZnMn3O7*3H2O Birnessite (Na,Ca)Mn7O14*2.8H2O Vernadite MnO2*nH2O Manganite MnOOH Groutite MnOOH Feitknechtite MnOOH Hausmannite Mn 2+ Mn 2 3+ O4 Bixbyite Mn2O3 Pyrochroite Mn(OH)2 Manganosite MnO Mn Oxide minerals (not all…) Wad

Iron Oxides Interaction of dissolved iron with oxygen yields iron oxide and iron oxyhyroxide minerals 1 st thing precipitated  amorphous or extremely fine grained (nanocrystaliine) iron oxides called ferrihydrite Fe 2+ O2O2

Ferrihydrite Ferrihydrite (Fe 5 O 7 OH*H 2 O; Fe 10 O 15 *9H 2 O  some argument about exact formula) – a mixed valence iron oxide with OH and water

Goethite Ferrihydrite recrystallizes into Goethite (  - FeOOH) There are other polymorphs of iron oxyhydroxides: – Lepidocrocite  -FeOOH – Akaganeite  -FeOOH

Iron Oxides Hematite (Fe 2 O 3 ) – can form directly or via ferrihydrite  goethite  hematite Red-brown mineral is very common in soils and weathering iron-bearing rocks

Magnetite (Fe 3 O 4 ) – Magnetic mineral of mixed valence  must contain both Fe 2+ and Fe 3+  how many of each?? ‘Spinel’ structure – 2/3 of the cation sites are octahedral, 1/3 are tetrahedral

Banded Iron Formations (BIFs) HUGE PreCambrian formations composed of hematite-jasper- chalcedony bands Account for ~90% of the world’s iron supply Occur only between 1.9 and 3.8 Ga  many sites around the world  Hammersley in Australia, Ishpeming in Michigan, Isua in Greenland, Carajas in Brazil, many other sites around the world…

BIFs and bacteria Early earth did not have free O 2, as microbial activity became widespread and photosynthetic organisms started generating O 2, the reduced species previously stable (without the O 2 ) oxidized – for Fe this results in formation of iron oxide minerals

Other important oxides Periclase, MgO – Met. mineral from dolomite Brucite, Mg(OH) 2 – weathering product Rutile, Anatase, brooksite- TiO 2 polymorphs Corundum, Al 2 O 3 – sapphire and ruby Ilmenite, FeTiO 3 – common in igneous/met. rx Cuprite, Malachite, Azurite – copper oxides Uraninite, UO 2 – important U ore Spinel, MgAl 2 O 4 – High-P met. mineral