MINERALS INDEX

Actinolite

Albite

Allactite

Allanite

Amphibole Group

Andradite

Anglesite

Anhydrite

Anorthite

Apatite

ApatiteGroup

Apophyllite

Aragonite

Arsenates

Arsenides

Arseniosiderite

Arsenopyrite

Aurichalcite

Axinite

Azurite

Barite

Barylite

Barysilite

Bementite

Biotite

Borates

Bornite

Boroarsenates

Bustamite

Cahnite

Calamine

Calcite

Calcium larsenite

Carbonates

Celestite

Cerusite

Chalcocite

Chalcophanite

Chalcopyrite

Chloanthite

Chlorite

Chlorophoenicite

Chondrodite

Chysolite Group

Clinohedrite

Copper

Corundum

Corundum Group

Crocidolite

Cummingtonite

Cuprite

Cuspidine

Cyprine

Datolite

Desaulesite

Descloizite

Diopside

Dolomite

Edenite

Epidote

EpidoteGroup

FeldsparGroup

Ferroaxinite

Ferroschallerite

Fluoborite

Fluorite

Franklinite

Friedelite

Friedelite Group

Gageite

Gahnite

Galena

Ganophyllite

Garnet

Glaucochroite

Goethite

Graphite

Greenockite

Gypsum

Halloysite

Haloids

Hancockite

Hardystonite

Hastingsite

Hedyphane

Hematite

Hetaerolite

Heulandite

Hodgkinsonite

Holdenite

Humite Group

Hyalophane

Hydrohetaerolite

Hydrozincite

Ilmenite

Jeffersonite

Kentrolite

Larsenite

Lead

Leucaugite

Leucophoenicite

Limonite

Lollingite

Loseyite

Magnesium- chlorophoenicite

Magnetite

Malachite

Manganbrucite

Manganite

Manganosite

Marcasite

Margarosanite

Mcgovernite

Mica Group

Microcline

Millerite

Molybdenite

Mooreite

Muscovite

Nasonite

Native Elements

Neotocite

Niccolite

Norbergite

Oxides

Pargasite

Pectolite

Phlogopite

Phosphates, Arsenates and Vanadates

Prehnite

Psilomelane

Pyrite

Pyrochroite

Pyroxene Group

Pyrrhotite

Quartz

Rhodochrosite

Rhodonite

Roeblingite

Roepperite

Rutile

Scapolite

Schallerite

Schefferite

Serpentine

Serpentine Group

Siderite

Silicates

Silver

Smithsonite

Sphalerite

Spinel

Spinel Group

Stilbite

Sulphates

Sulphides and Arsenides

Sussexite

Svabite

Talc

Tennantite

Tephroite

Thomsonite

Thorite

Titanite

Tourmaline

Tremolite and Actinolite

Unconfirmed Species

Vanadates

Vesuvianite

Willemite

Xonotlite

Zeolites

Zinc schefferite

Zincite

Zircon

Zoisite

 

Chalcophanite

(Mn,Zn,Fe)O.2MnO2.2H2O
Hexagonal-rhombohedral

Forms
c(0001), r(1011)

Habit
Chalcophanite forms minute crystals tabular parallel to the base, or with the base and rhombohedron in equal development, giving an octahedral habit.

fig55.gif (3869 bytes) Figure 55
Hexagonal tabular crystal of chalcophanite showing the c(0001) and r(1011). Sterling Hill.

It is commonly in lamellar aggregates, either crusts or stalactites, the plates being nearly perpendicular to the surface of attachment. Much of it is deposited on botryoidal surfaces of hydrohetaerolite or limonite or lines cavities with drusy surfaces. Such drusy crusts have a peculiar bluish-black color and a brilliant metallic luster, especially on freshly broken surfaces, owing to the perfect basal cleavage. The specific gravity is 3.903 (Moore, 108), and that of hydrofranklinite is 4.01 to 4.09 (Penfield and Kreider, 157). The mineral is uniaxial, negative, nearly opaque, and strongly pleochroic— e = deep red, w = nearly opaque; w > 2.7 (Larsen).

Composition
The following analyses show the composition of chalcophanite:

Analyses of chalcophanite
 

1

2

3

 

Percent

Ratio

Percent

Ratio

Percent

Ratio

MnO2

59.94

2

61.57

2

58.48

2

MnO

6.58

1.04*

4.41

0.9*

   
ZnO

21.70

 

20.80

 

18.25

1.07†

FeO        

10.00

 
H2O

11.58

1.87

12.66

2

11.85

1.94

Fe2O3

0.25

         
Insoluble        

0.25

 
 

100.05

 

99.44

 

99.83

 
[* figures represent combined MnO + ZnO]
[* figure represents combined ZnO + FeO]
1. Crystals. G. E. Moore (108), analyst.
2. Stalactitic masses, after deducting 1.27 percent for limonite. G. E. Moore (108), analyst.
3. Hydrofranklinite, minute crystals. Penfield and Kreider (157), analysts.

Analysis 3 differs from the others in the presence of much FeO, but all three approximate closely in ratios the same expression: RO : MnO2 : H2O = 1 : 2 : 2, giving the formula as adopted.

Occurrence
Chalcophanite is known only from Sterling Hill, where it was discovered and described by Moore (108), then chemist for the Passaic Zinc Company. He states that it was found in cavities and fissures in a mass of debris made up of waterworn fragments of quartz and other rocks and of more or less decomposed franklinite, willemite, and zincite. This mass of material was commonly called the "stripping" of the calamine deposit at the Passaic mine and was used to some extent as an ore of manganese.

In 1882 Roepper (124) announced a new hydrous oxide of zinc, iron, and manganese, found at Sterling Hill in the form of octahedrons, and gave to it the name "hydrofranklinite." His investigation was unfinished at his death, but Penfield and Kreider (157), on analyzing similar material, found it to be the same as chalcophanite, its apparent octahedral form being due to the habit of the rhombohedral crystals (figure 56).

Figure 56
Rhombohedral crystal of chalcophanite of octahedron-like habit, showing the forms c(0001) and r(1011). Sterling Hill.
fig56.gif (6414 bytes)

Its composition and mode of occurrence indicate clearly that chalcophanite is an alteration product of franklinite. Moore believed that franklinite was first changed to hydrohetaerolite—2ZnO.2Mn2O3.H2O, the iron being partly eliminated as limonite—and then by oxidation and further hydration the hydrohetaerolite was in turn changed to chalcophanite.4 The facts that chalcophanite is invariably found surrounding hydrohetaerolite where the two occur together and that some franklinite crystals, deeply etched, have been found coated in turn by hydrohetaerolite and chalcophanite give strength to Moore's theory of the origin of those peculiar and very local minerals.

4 From a note by Moore, appended to a specimen of hydrohetaerolite In the Roebling collection.

 


 
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