One of the most important economic questions of the present day is the preservation of iron and steel structures. In America many millions of dollars are annually spent in the erection and construction of these, and the amount is increasing in rapid proportion. Bridges, buildings, viaducts, ships, and machinery are now being made of these materials, to almost the entire exclusion of others. From their very nature iron and steel are peculiarly subject to decay from atmospheric and other influences. The question of preserving them is not merely one of finance, but, especially in the case of railroads, one affecting the lives and property of a large portion of the community. What, then, is the best method of preserving them?
The almost universal method is by means of paints, or the application of substances to their surfaces which will resist or retard the influence of air, water, and other destructive agencies. The requisites of a good paint for this purpose are that it shall adhere firmly to the surface, and not chip or peel off, thereby leaving portions of the surface exposed. It must not corrode the iron, else the remedy may only aggravate the disease. It must form a surface hard enough to resist influences which would remove it by friction, yet elastic enough to conform to the expansion and contraction of the metal by heat and cold. It must be impervious to and unaffected, as far as possible, by moisture, atmospheric and other influences to which the structure may be exposed.
The paints that have been used for this purpose are principally asphalt and coal-tar paints, consisting of mineral and artificial asphalt or coal-tar, either applied alone or combined with each other, and, more or less, with metallic bases, and iron oxide paints and lead oxide paints, especially red lead, in all of which the pigment is held to the surface of the iron or steel by combination with linseed oil. The choice of paints must lie, so far as our present practical experience goes, between these three classes, zinc oxide being found to be entirely unsuitable on account of a propensity to peel off. What, then, is found to be the experience in actual practice with these? Asphalt and coal-tar paints “run” when exposed to the sun and other sources of heat, which is a serious matter with vertical surfaces; and after a time become extremely brittle and scale off entirely, leaving the under surface exposed, unless the paint is constantly renewed. In the meantime the exposed iron and steel are being corroded by rust. Iron oxide paints, including “metallic brown,” are paints made from iron ore, or by some chemical process with an iron base. These are invariably iron in a greater or less degree of oxidation, or in other words, rusted iron. Now it is well known that one of the most active promoters of rust or decay in iron is the rust itself. Under the combined influences of the moisture and carbonic acid of the atmosphere, iron oxide or iron rust becomes a carrier of oxygen from the air to the metal, rust begetting rust. It is therefore evident that this material alone has no preserving effect on iron; in fact, it promoted its decay.
How is it when combined with linseed oil in the form of paint? In the economy of nature, iron oxide is a great disinfectant. When in contact with organic matter and moisture, even at a low temperature, under favourable conditions, it readily gives up oxygen, destroying more or less the organic matter, and being itself reduced to a lower oxide. When thus reduced, with equal readiness it absorbs oxygen from the atmosphere, and again passes it on, thereby promoting and eventually ensuring the destruction or transformation of the organic matter with which it may be in contact, either in the soil or elsewhere. The same process appears to take place when combined with linseed oil in the form of paint and exposed to atmospheric influences, the oil being the organic matter. If linseed oil in drying formed an air-and water-proof film, it might be urged that the oxide of iron would be entirely protected from the direct influences of oxygen of the air and moisture. Such however is not the case.
The most eminent authorities have recently shown that the dried film of linseed oil, unless united with a pigment that combines chemically and forms a water-proof coating with it, actually absorbs water very much like a sponge. Where water will go air will also go, and we thus have in direct contact with the iron oxide of the paint, which does not combine chemically with oil, those elements, air, moisture, and organic matter, which cause the iron to become a carrier of oxygen and a destroyer of what it is in contact with. It is well known that iron paint darkens with age; this is caused largely by the iron oxide losing oxygen, which is partly transferred to the oil, burning it up and destroying its tenacity, as may be seen by examining iron structures painted for some time with iron paint or metallic brown, the paint being found extremely brittle and in feathery scales. This is not all the damage that is done. The iron oxide in the paint becomes a carrier of oxygen to the very metal it was designed to protect, and the process of corrosion is commenced and carried on under the paint, which eventually peels or scales off, the surface of the metal being found more or less oxidised and corroded.
Asphalt and iron oxide being thus shown to be entirely incapable of preserving the iron, it remains for us to consider the effect of red lead. This pigment has the property of forming with linseed oil a hard elastic coating, clinging with great tenacity to the metal. It has no oxidising effect on iron, and does not act as a carrier of oxygen from the atmosphere after the paint has set, neither does it render the oil brittle nor promote rust. When red lead fails, it is principally by gradual wear or friction from the outside. It does not scale or blister, which both asphalt and iron oxide paints will do, thereby requiring a thorough scraping and removal of old material before a new coat can be applied. Any red lead pigment adhering to the metal forms a permanent base for subsequent paintings, and is utilised in further preserving the metal. The U.S. Government specifications for ironwork in the new Library Building of Congress provide that “all the work not Bower-Barffed must be given one coat of pure red lead paint—not metallic paint of any kind, but pure red lead—before leaving the shop and becoming rusted.”
The experiments of the U.S. Navy Department on the preservation and fouling of plates covered with different pigments may be interesting. A plate of iron covered with asphalt paint was immersed in sea-water for eight months and six days at the U.S. Navy Yard, Portsmouth, N.H. At the end of that period it was found to be covered with scum and mud, and very badly rusted. A plate coated with iron paint, immersed at Key West, Fla., was found to be covered with branch shell and coral, but little paint remaining, and very badly pitted and rusted. A plate with two coats of red lead, at the Norfolk Navy Yard, was found to have a few barnacles attached, but to be in fair condition, with no rust whatever on the iron after the paint was removed. It will be seen that not only did the red lead protect the iron better than the other pigments referred to, but that the plates were in far better condition as regards barnacles and fouling. The superiority of red lead being thus established, it is adopted for use on hulls of U.S. Government warships.
On the Dutch State railroads a series of experiments extending over a period of three years were made with the above pigments on scrubbed plates, as well as those which had been pickled in acid to remove the scale. It was found that the red lead was superior in each case to the others.
If red lead is thus proved to be the best pigment for preserving iron and steel structures, what is the proper method for applying it? We have seen above that the value of red lead depends upon its forming certain combinations with the oil, and actually setting very much the same as plaster of Paris or cement sets when mixed with water. To successfully work with the latter substances, it is necessary to put them in shape as quickly as possible after mixing with water before the setting takes place. If the chemical action of setting has partly taken place, the material may be moulded, but it is known that good results will not be obtained. Red lead, like these substances, must be applied to the work before it sets with the oil. It is on this point that failures in the use of pigment have generally occurred, because if it be applied after the combining or setting process has taken place, the hard, elastic, clinging coating will not be formed on the iron surface.
The following is the practice of one of the largest shipbuilding establishments in applying red lead to the hulls of vessels. The plates are first pickled in a dilute solution of muriatic acid; then passed between rapidly revolving wire brushes, which remove all scale and dirt, leaving the iron with a bright, smooth surface; then thoroughly washed with pure water, and rubbed entirely dry; and immediately coated with red lead and pure raw linseed oil. The red lead is first thoroughly mixed with just enough linseed oil to form a very thick, tough paste, which will keep for several days without hardening. This paste, as wanted for use, is thinned down to the proper consistency for spreading with pure linseed oil, and applied at once, care being taken to leave paint-pots empty at night. A gallon of paint thus prepared contains about 5 lb. of oil and 18 lb. of red lead, and will cover on first coat about 500 square feet. In this way the red lead and oil get their initial set on the surface of the iron, and the closer the pigment is brought to the iron the more durable will it be found. Some parties prime iron with iron oxide paint or metallic brown before applying red lead, which appears to be a mistake, as this paint readily scales from iron, and, of course, carries the lead with it. Others coat the iron with oil before applying the red lead. This, too, prevents the adhering paint from coming in contact directly with the surface, and should be avoided, provided the iron is properly prepared by thorough cleaning and removal of any scale and moisture, which is a matter of the greatest importance.