Potassium Iodide, KI. It may be purchased nearly pure. It is used as a test and for dissolving iodine. It should be used in a 10 per cent. solution freshly made. The solution decomposes on exposure to light, with separation of iodine.

Potassium Nitrate (KNO3) can be purchased pure. It is used in the dry way as an oxidizing agent. It is very fusible. It decomposes at a low temperature into potassium nitrite (KNO2) and free oxygen; and at a higher temperature leaves potash (K2O). It oxidizes sulphur and carbon with explosive violence. This action may be moderated by mixing the nitre with carbonate of soda, common salt, or some other inert body.

Potassium Nitrite, KNO2.—The commercial article is not pure, but is sufficiently so for the purpose required. A saturated solution is used in the separation of cobalt; the solution is made when wanted.

Potassium Permanganate, KMnO4.—This salt can be purchased sufficiently pure. It is much used as an oxidizing agent.

Potassium Bisulphate (KHSO4) is used as a dry reagent for opening up minerals. It fuses; and at a much higher temperature is converted into potassium sulphate with loss of sulphuric acid.

Potassium Sulphocyanate (KCNS) is used for the detection and determination of traces of ferric iron; as also in the separation of silver and copper from some of the other metals. Make a 10 per cent. solution. It should show no colour on the addition of hydrochloric acid.

"Red Lead" (Pb3O4) is used in the dry assay as a flux instead of litharge, from which it differs in containing a little more oxygen. When acted on by nitric acid a brown residue of lead dioxide is left, nitrate of lead going into solution. Like litharge it always carries silver; about 2 milligrams in 100 grams.

Silver, Ag.—Pure silver in foil is required as a standard. It may be prepared as follows:—Dissolve scrap silver in dilute nitric acid and decant off from any residue; dilute the solution with hot water and add hydrochloric acid until there is no further precipitate, stir; allow the precipitate to settle; decant and wash; dry the precipitate, mix it with twice its bulk of carbonate of soda and fuse the mixture in a crucible until tranquil; clean the button and roll or hammer it into foil.

Sodium Acetate, NaC2H3O2.3H2O.—The crystals may be purchased sufficiently pure. Make a 20 per cent. solution in water. It is used for replacing mineral acids by acetic acid.[7]

Sodium Acetate and Acetic Acid.—A solution is used in the determination of phosphates and arsenates; 100 grams of the salt is dissolved in 500 c.c. of acetic acid, and diluted with water to one litre.