MINERALS INDEX
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.
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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:
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1 |
2 |
3 |
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|
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* |
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| ZnO |
21.70 |
20.80 |
18.25 |
1.07 |
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| FeO |
10.00 |
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| H2O |
11.58 |
1.87 |
12.66 |
2 |
11.85 |
1.94 |
| Fe2O3 |
0.25 |
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| Insoluble |
0.25 |
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|
100.05 |
99.44 |
99.83 |
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| [* 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. |
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Its composition and mode of occurrence indicate clearly that chalcophanite is an alteration product of franklinite. Moore believed that franklinite was first changed to hydrohetaerolite2ZnO.2Mn2O3.H2O, the iron being partly eliminated as limoniteand 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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Website
© by Herb Yeates 1997-2001.
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page created: January 12, 2001 5:52 PM
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