| Copper | 99.46 | per cent. |
| Bismuth | 00.30 | " |
| Iron | 00.14 | " |
| Arsenic | 00.10 | " |
| ——— | ||
| 100.00 |
The quantity of copper got in each assay was 0.175 gram, and consequently the bismuth averaged 0.00053 gram.
To separate the bismuth in such a case the deposit is dissolved off by warming it in the original solution. The bismuth is precipitated by the addition of ammonic carbonate, and the solution, after filtering and acidifying with nitric acid, is re-electrolysed.
Determination of Copper in Commercial Copper.—Take from 1 to 1.5 gram, weigh carefully, and transfer to a beaker; add 20 c.c. of water and 10 c.c. of nitric acid; cover with a clock glass, and allow to dissolve with moderate action; boil off nitrous fumes, dilute to 100 c.c., and electrolyse. The cylinder must be carefully weighed, and the electrolysis allowed to proceed for 24 hours. The weight found will be that of the copper and silver. The silver in it must be determined[53] and deducted.
Determination of Copper in Brass, German Silver, or Bronze.—Treat in the same manner as commercial copper. If nickel is present, the few milligrams of copper remaining in the electrolysed solution should be separated with sulphuretted hydrogen, the precipitated sulphide dissolved in nitric acid, and determined colorimetrically.
VOLUMETRIC PROCESSES.
There are two of these in use, one based on the decolorising effect of potassic cyanide upon an ammoniacal copper solution, and the other upon the measurement of the quantity of iodine liberated from potassic iodide by the copper salt. The cyanide process is the more generally used, and when carefully worked, "on certain understood and orthodox conditions," yields good results; but probably there is no method of assaying where a slight deviation from these conditions so surely leads to error. An operator has no difficulty in getting concordant results with duplicate assays; yet different assayers, working, without bias, on the same material, get results uniformly higher or lower; a difference evidently due to variations in the mode of working. Where a large number of results are wanted quickly it is a very convenient method. The iodide process is very satisfactory when worked under the proper conditions.
CYANIDE METHOD.
The process is based upon the facts—(1) that when ammonia is added in excess to a solution containing cupric salts, ammoniacal copper compounds are formed which give to the solution a deep blue colour; and (2) that when potassic cyanide is added in sufficient quantity to such a solution the colour is removed, double cyanides of copper and potassium or ammonium being formed.[54] In the explanation generally given the formation of cuprous cyanide is supposed[55]; but in practice it is found that one part of copper requires rather more than four parts of cyanide, which agrees with the former, rather than the latter, explanation.