The Journal of Geology, May-June 1893: A Semi-Quarterly Magazone of Geology and Related Sciences — John Shaqi
The Journal of Geology, May-June 1893: A Semi-Quarterly Magazone of Geology and Related SciencesVarious
Science
The Journal of Geology, May-June 1893: A Semi-Quarterly Magazone of Geology and Related Sciences
Various
Geology -- Periodicals
THE FORMS OF IRON AND MANGANESE DEPOSITED AT ORDINARY TEMPERATURES.
The mineralogical forms in which iron and manganese are deposited from
solution in nature at ordinary temperatures depend on the conditions
of air and water, whether of an oxidizing or a reducing nature, and on
the character of the associated organic and inorganic matter either
in solution or on the floor of the sea, lagoon or bog in which the
deposition occurs.[18] There are four principal methods by which iron
and manganese are precipitated in nature from surface waters:
(1) By oxidation, as in the case of the precipitation of hydrous oxides
and in the precipitation of the carbonate by the partial oxidation of
more complex organic salts.[19]
(2) By reduction, as in the precipitation of sulphide of iron by the
reduction of sulphate of iron.
(3) By gaseous or soluble precipitants, as in the precipitation of
sulphide of iron by the action of sulphuretted hydrogen or a soluble
sulphide on a soluble salt of iron, and as in other cases to be
mentioned later.
(4) By replacement of carbonate of lime or some other substance.
Different forms are precipitated by these different methods.
Iron at ordinary temperatures is usually deposited from solution as
the hydrous sesquioxide, the carbonate, the sulphide or the hydrous
silicate of iron and potash known as glauconite. Manganese under
similar conditions is deposited as the hydrous oxide[20] or as the
carbonate, and possibly sometimes, though very rarely, as sulphide.
When solutions of organic or inorganic salts of iron and manganese are
freely exposed to the action of air, as in shallow or rapidly moving
streams, or in lakes and some bogs, they are quickly oxidized and
both may be deposited as more or less hydrous oxides. In many bogs,
however, the metals may be precipitated as hydrous oxide on the surface
where oxidizing agencies predominate, but when these oxides sink and
come into contact with decaying organic matter, free from the active
oxidizing influences of the air, they may be reduced to carbonates.
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