In 1866 the great Calumet and Hecla mine at Lake Superior commenced operations, and speedily became one of the most important sources of copper in the world; the Moonta and Wallaroo mines in Australia opened about the same time, and in 1873 the Arizona mines started producing. In 1876 the enormous Spanish mines at Rio Tinto were re-opened, and soon rendered available large quantities of ore. Later, the Tasmanian supplies entered the markets.

In 1880 a remarkable development in copper mining occurred with the discovery of the Butte camp in Montana; this is now the greatest producer in the world.

The later extensions of the copper mining industry occurred in Utah, Tennessee, and Queensland, whilst within recent years the most important work on a large scale has been commenced in Tanganyika, in Nevada, and in Siberia.

The developments in the smelting industry in most of these localities have proceeded, until the last few years, on very similar lines. During the first periods following the opening up of mines and works, ore was shipped to the custom smelters, most often to Swansea; where, in the early days, many of those connected with the smelting works had some sort of financial interest in the foreign mines. Later, the ore underwent its first smelting to matte in the mining district itself, the matte product being then shipped East for treatment, thus saving much of the freight-charge on useless gangue, as well as smelters’ heavy returning charges, etc. At a later period the smelting operation was carried to a still further stage in the mining district, crude blister copper only being sent to Swansea or elsewhere to be refined.

Gradually, electrolytic refineries were established somewhat nearer to the mining districts, and in the natural course of events, and where local conditions are not prohibitive, the probability is that the whole cycle of operations from mining to the production of refined market metal will be carried out at the great camps themselves.

At present, however, this is not generally the case, since the conditions under which the enormous refineries in the Eastern States of New York, New Jersey, and in Baltimore, etc., operate, allow of the cheaper production of electrolytic copper at points nearer to the distributing markets. At Anaconda, indeed, the fully-equipped electrolytic plant was shut down, owing to the commercial conditions such as have just been indicated, having rendered the refining of the anode copper at the Eastern refineries more profitable than electrolytic treatment on the spot.

The Chief Features in the Development of Modern Copper Smelting Practice.—In the early days of copper smelting, the reduction of the oxidised ores, which were then chiefly available, was not a problem of very great difficulty, although losses in slag were likely to be very high, and the operation generally wasteful. When, however, mines became deeper and sulphide ores had to be smelted, the problem became rather more complicated. In the first stages of development, such ores were probably roasted until as much sulphur as possible had been driven off, leaving practically an oxide charge to be treated by the older reduction methods involving the attendant extravagance in fuel consumption and large losses of copper in the slag.

From these crude and wasteful methods the Welsh process was gradually worked out, and it will ever rank as one of the finest examples of highly developed smelting practice in the history of metallurgy, particularly when the times and working conditions are borne in mind. The process having received such full treatment from most of the common text-books, it is not proposed to review it in detail here, since, moreover, it has been largely superseded by more modern processes.

As will be explained later, copper smelting of sulphide ores is essentially a fractional oxidation—chiefly of iron and sulphur—followed by the slagging or elimination of extraneous constituents of the ore. The Welsh process embodied a series of roastings and slaggings which, though most admirably adjusted for a substantial concentration of the copper in each succeeding product, allowed of the formation of slags in the first stages which carried but comparatively little copper, on account of the low tenor of the matte; whilst the slags in the later stages of the process, containing more copper on account of their association with higher grade matte, were made in such relatively small quantity that their re-treatment for the recovery of these values did not involve very much loss of efficiency in the furnace operations.

Later modifications of the process were chiefly devised with the view to reducing the number of operations, by eliminating the successive roasting stages, for which purpose oxidised materials, such as roasted or oxidised ores, were added to the charge.