Geologic Features

The antimony sulphide, stibnite, is the source of most of the world's production of this metal. Antimony oxides, including senarmontite, cervantite, and others, are formed near the surface, and in some of the deposits of Mexico and Algeria they supply a large part of the values recovered. Jamesonite, bournonite, and tetrahedrite (sulphantimonides of lead and copper), when found in lead-silver deposits, are to some extent a source of antimony in the form of antimonial lead.

Stibnite is found in a variety of associations and is present in small quantities in many types of deposits. In the commercial antimony deposits, it is in most cases accompanied by minor quantities of other metallic sulphides—pyrite, cinnabar, sphalerite, galena, arsenopyrite, etc.—in a gangue of quartz and sometimes calcite. Many of the deposits contain recoverable amounts of gold and silver.

The deposits of the Hunan Province of southern China occur as seams, pockets, and bunches of stibnite ore in gently undulating beds of faulted and fissured dolomitic limestone. In the vicinity of the most important mines no igneous rocks have been observed, and the origin of the ores has not been worked out.

In the Central Plateau of France the numerous antimony deposits are stibnite veins cutting granites and the surrounding schists and sediments. An origin related in some way to hot ascending solutions seems probable.

The deposits of the National district of western Nevada, the most important war-developed antimony deposits of the United States, consist of stibnite veins with a gangue of fine-grained drusy quartz, cutting through flows of rhyolite and basalt. They are intimately related to certain gold- and silver-bearing veins, and all are closely associated with dikes of rhyolite, which were the feeders to the latest extrusion in the district. The wall rocks have undergone alteration of the propylitic type. These relations, and the presence of the mercury sulphide, cinnabar, in some of the ores (see pp. 258-259), suggest an origin through the work of ascending hot waters or hot springs. These waters probably derived their dissolved matter from a magmatic source, and worked up along vents near the rhyolite dikes soon after the eruption of this rock.

In the weathering of antimony deposits, the stibnite usually alters to form insoluble white or yellowish oxides, which are sometimes called "antimony ocher." These tend to accumulate in the oxide zone through the removal of the more soluble accompanying minerals. Secondary sulphide enrichment of antimony deposits, if it occurs at all, is negligible.

ARSENIC ORES

Economic Features

About two-thirds of the arsenic consumed in recent years has been used in agriculture, where various arsenic compounds—arsenic trioxide or "white arsenic," Paris green, lead arsenate, etc.—are used as insecticides and weed killers. Arsenic compounds are also used in "cattle-dips" for killing vermin. The only other large use of arsenic is in the glass industry, arsenic trioxide being added to the molten glass to purify and decolorize the product. Small quantities of arsenic compounds are used in the preparation of drugs and dyeing materials, and metallic arsenic is used for hardening lead in shot-making.

The principal arsenic-producing countries are the United States, Germany, France, Great Britain, Canada, and Mexico. Spain, Portugal, Japan, and China are also producers, and recent trouble with the "prickly-pear" pest in Queensland, Australia, has led to local development of arsenic mining in that country. For the most part, European production has been used in Europe and American production in the United States.

Arsenic is recovered almost wholly as a by-product of smelting ores for the metals. The potential supply is ample in most countries where smelting is conducted, but owing to the elaborate plant required to recover the arsenic, apparatus is not usually installed much in advance of the demand for production. Rapid expansion is not possible.

Before the war the arsenic needs of the United States (chiefly agricultural) were supplied by a few recovery plants in the United States, Mexico, and Canada. Several large smelters had not found it profitable to install recovery plants, as the market might have been oversupplied and prices were low. During the war, with the extensive demand for insecticides for gardening, there was a considerable deficiency of arsenic supplies. With rising prices production was stimulated, but was still unable to meet the increased demand. This situation resulted in regulation of the prices of white arsenic by the Food Administration.

Production of arsenic in the United States comes chiefly from smelters in Colorado, Washington, Utah, Montana, and New Jersey. Small amounts are produced by arsenic mines in Virginia and New York. A Mexican plant at Mapimi has been shipping important quantities to the United States. The plant at Anaconda, Montana, is expected to produce an ample supply in the future.

The United States is entirely independent in arsenic supplies and will probably soon have an exportable surplus. Export trade, after the reconstruction period, will probably meet competition from France and Germany where production was formerly large.