- portion of a hundredth it prevents the action of the water almost entirely;
but if the proportion be diminished to a 160th, the loss sustained by the lead is fully a third of the loss in distilled water.
When lead has been exposed for a few weeks to a solution of a protecting salt and has acquired a thin film over its surface, it not only is not acted on by the solution, but is even also rendered incapable of being acted on by distilled water.
The preservative power depends on the acid, not on the base of the salt. The acetate, muriate, arseniate, and phosphate of soda differ exceedingly in power. On the other hand, the sulphates of soda, magnesia, and lime, as well as the triple sulphate of alumina and potass, preserve as nearly as can be determined in the same proportion.
When we attempt to ascertain the relative preserving power of the neutral salts, it will appear that those whose acid forms with the lead a soluble salt of lead are the least energetic; while those whose acid forms an insoluble salt of lead are most energetic. The protecting powers of acetate of soda, nitrate of potass, muriate of soda, sulphate of lime, arseniate of soda, and phosphate of soda, are inversely as the solubility of the acetate, nitrate, muriate, sulphate, arseniate, and phosphate of lead. The existence of this ratio might naturally lead to the inference that the protecting power depends simply on the salt in solution being decomposed, so that there is formed on the surface of the lead a thin crust consisting of the oxide of the metal in union with the acid of the decomposed salt, and constituting an insoluble film which is impermeable to aërated water: for example, that phosphate of soda acts in the small proportion of a 30,000th part by forming on the surface of the metal an impermeable film of phosphate of lead, which is known to be one of the most insoluble of all the neutral salts. But this is not altogether a correct statement of the fact.
When the protection afforded is complete, as for example by a 27,000th of phosphate of soda, a 12,000th of arseniate of soda, or a 4000th of sulphate of soda, the lead undergoes no change in appearance or in weight for several hours, or even days. At length the surface becomes dull, then white, and gradually a uniform film is formed over it. This film, examined at an early period, is found to consist of carbonate of lead,—being entirely soluble in diluted acetic acid, although the salts in solution is a sulphate or phosphate. But after a few weeks the carbonate is mixed with a salt of lead, containing the acid of a part of the neutral salt dissolved in the water: if, after five or six weeks' immersion in a preservative solution of phosphate or sulphate of soda, the film on the lead be scraped off and immersed in diluted acetic acid, effervescence and solution take place, but a part of the powder remains undissolved; and if the protecting salt has been the muriate of soda, the whole powder is dissolved, but muriatic acid will be found in solution by its proper test, the nitrate of silver.—In all such protecting solutions the lead gains weight for some weeks; but at length it ceases to undergo farther change, and is not acted on even if removed into distilled water.
