SECTION VII.

GALVANIZING.

Galvanizing, as a protecting surface for large articles, such as enter

into the construction of bridges, roofs, and shipwork, has not quite

reached the point of appreciation that possibly the near future may

award to it. Certain fallacies existed for a long time as to the

relative merits of the dry or molten and the wet or electrolytical

methods of galvanizing. The latter was found to be costly and slow,

and the results obtained were erratic and not satisfactory, and soon

gave place to the dry or molten bath process, as in practice at the

present day; but the difficulty of management in connexion with large

baths of molten material, and the deterioration of the bath, and other

mechanical causes, limit the process to articles of comparatively

small size and weight. The electro deposition of zinc has been subject

to many patents, and the efforts to introduce it have been lamentable

in both a mechanical and financial sense. Most authorities recommend a

current density of 18 or 20 ampères per square foot of cathode

surface, and aqueous solutions of zinc sulphate, acetate or chloride,

ammonia, chloride or tartrate, as being the most suitable for

deposition. Electrolytes made by adding caustic potash or soda to a

suitable zinc salt have been found to be unworkable in practice on

account of the formation of an insoluble zinc oxide on the surface of

the anode and the resultant increased electrical resistance; the

electrolytes are also constantly getting out of order, as more metal

is taken out of the solution than could possibly be dissolved from the

anodes by the chemicals set free on account of this insoluble scale or

furring up of the anodes, which sometimes reaches one-eighth of an

inch in thickness. To all intents and purposes the deposits obtained

from acid solutions under favourable circumstances are fairly adhesive

when great care has been exercised to thoroughly scale and clean the

surface to be coated, which is found to be the principal difficulty in

the application of any electro-chemical process for copper, lead, or

tin, as well as for zinc, and that renders even the application of

paint or other brush compounds to futile unless honestly complied

with. Unfortunately these acid zinc coatings are of a transitory

nature, Their durability being incomparable with hot galvanizing, as

the deposit is porous and retains some of the acid salts, which cause

a wasting of the zinc, and consequently the rusting of the iron or

steel. Castings coated with acid zinc rust comparatively quickly, even

when the porosity has been reduced by oxidation, aggravated no doubt

by some of the corroding agents--sal-ammoniac, for instance--being

forced into the pores of the metal. Other matters of serious moment in

the electro-zincing process, apart from the slowness of the operation,

were the uncertain nature, thickness, and extent of the coating on

articles of irregular shape, and the formation of loose, dark-coloured

patches on the work; the unhealthy and non-metallic look and want of

brilliancy and the lustre prevented engineers and the trade from

accepting the process or its results, except for the commoner articles

of use. To obviate any tendency of the paint to peel off from the zinc

surface, as it generally manifests a disposition to do, it is

recommended to coat all the zinc surfaces, previous to painting them,

with the following compound: 1 part chloride of copper, 1 part nitrate

of copper, 1 part sal-ammoniac, dissolved in 61 parts of water, and

then add 1 part commercial hydrochloric acid. When the zinc is brushed

over with this mixture it oxidizes the surface, turns black, and dries

in from twelve to twenty-four hours, and may then be painted over

without any danger of peeling. Another and more quickly applied

coating consists of, bi-chloride of platinum, 1 part dissolved in 10

parts of distilled water, and applied either by a brush or sponge. It

oxidizes at once, turns black, and resists the weak acids, rain, and

the elements generally.

Zinc surfaces, after a brief exposure to the air, become coated with a

thin film of oxide--insoluble in water--which adheres tenaciously,

forming a protective coating to the underlying zinc. So long as the

zinc surface remains intact, the underlying metal is protected from

corrosive action, but a mechanical or other injury to the zinc coating

that exposes the metal beneath, in the presence of moisture causes a

very rapid corrosion to be started, the galvanic action being changed

from the zinc positive to zinc negative, and the iron, as the positive

element in the circuit, is corroded instead of the zinc. When

galvanized iron is immersed in a corrosive liquid, the zinc is

attacked in preference to the iron, provided both the exposed parts of

the iron and the protected parts are immersed in the liquid. The zinc

has not the same protective quality when the liquid is sprinkled over

the surface and remains in isolated drops. Sea air, being charged with

saline matters, is very destructive to galvanized surfaces, forming a

soluble chloride by its action. As zinc is one of the metals most

readily attacked by acids, ordinary galvanized iron is not suitable

for positions where it is to be much exposed to an atmosphere charged

with acids sent into the air by some manufactories, or to the

sulphuric acid fumes found in the products of combustion of rolling

mills, iron, glass, and gas works, etc., and yet we see engineers of

note covering-in important buildings with corrugated and other sheets

of iron, and using galvanized iron tie rods, angles, and other

constructive shapes in blind confidence of the protective power of the

zinc coating; also in supreme indifference as to the future

consequences and catastrophes that arise from their unexpected

failure. The comparative inertia of lead to the chemical action of

many acids has led to the contention that it should form as good, if

not a better, protection of iron than zinc, but in practice it is

found to be deficient as a protective coating against corrosion. A

piece of lead-coated iron placed in water will show decided evidences

of corrosion in twenty-four hours. This is to be attributed to the

porous nature of the coating, whether it is applied by the hot or wet

(acid) process. The lead does not bond to the plate as well as either

of the other metals--zinc, tin, copper, or any alloys of them. The

following table gives the increase in weight of different articles due

to hot galvanizing:--

+--------------------------+--------------------------+-------------+

| Description of | Weight of Zinc | Percentage |

| Article | per Square foot | of Increase |

| | | of Weight |

+--------------------------+--------------------------+-------------+

| Thin sheet-iron | 1.196 oz. | 18.2 |

| 5/16-in. plates | 1.76 " | 2.0 |

| 4-in. cut nails | 2.19 " | 6.72 |

| 7/8-in. die bolt and nut | approximately 1.206 oz. | 1.00 |

+--------------------------+--------------------------+-------------+

Tin is often added to the hot bath for the purpose of obtaining a

smoother surface and larger facets, but it is found to shorten the

life of the protective coating very considerably.

A portion of a zinc coating applied by the hot process was found to be

very brittle, breaking when attempts were made to bend it; the average

thickness of the coating was .015 inch. An analysis gave the following

result: tin, 2.20; iron, 3.78; arsenic, a trace; zinc (by difference),

94.02. A small quantity of iron is dissolved from all the articles

placed in the molten zinc bath, and a dross is formed amounting in

many cases to 25 per cent of the whole amount of zinc used. The

zinc-iron alloy is very brittle, and contains by analysis 6 per cent

of iron, and is used to cast small art ornaments from. A hot

galvanizing plant, having a bath capacity of 10 feet by 4 feet by

4-1/2 feet outside dimensions, and about 1 inch in thickness, will

hold 28 tons of zinc. With equal amounts of zinc per unit of area, the

zinc coating put on by the cold process is more resistant to the

corroding action of a saturated solution of copper sulphate than is

the case with steel coated by the ordinary hot galvanizing process;

or, to put it in another form, articles coated by the cold process

should have an equally long life under the same conditions of exposure

that hot galvanized articles are exposed to, and with less zinc than

would be necessary in the ordinary hot process. The hardness of a zinc

surface is a matter of some importance. With this object in view

aluminium has been added from a separate crucible to the molten zinc

at the moment of dipping the article to be zinced, so as to form a

compound surface of zinco-aluminium, and to reduce the ashes formed

from the protective coverings of sal-ammoniac, fat, glycerine, etc.

The addition of the aluminium also reduces the thickness of the

coating applied. Cold and hot galvanized plates appear to stand

abrasion equally well. Both pickling and hot galvanizing reduce the

strength, distort and render brittle iron and steel wires of small

sections.

THE END.

INDEX.

A

Amalgam process in tin-plating, 59.

Appliances and apparatus used in japanning and enamelling, 29.

B

Battery process in tin-plating, 59.

Black grounds, 11.

---- japan grounds on metal, common, 12.

---- paints, 52.

---- pigment, 46.

---- stain for iron, 53.

---- varnish for sewing machines, 56.

Blue japan grounds, 9.

---- pigment, 46.

Brass, polished, colours for, 49-57.

Brick ovens, 33.

Bright pale yellow grounds, 10.

Bronzing composition, 49.

Brown japan, 57.

Bunsen burner, 33.

C

Carriage varnish, 51.

Colours for polished brass, 49.

Common black japan grounds on metal, 12.

Composition for bronzing, 49.

Cream enamel, 8.

E

Enamelling and japanning stoves, 29-46.

---- ---- ---- ---- heated by direct fire, 34.

---- ---- ---- ---- heated by hot-water pipes, 36.

---- or japanning metals, 20-28.

---- old work, 27.

F

First stage in the japanning of wood, 5.

---- ---- in the japanning of leather, without a priming, 5.

G

Galvanized iron, painting on, 49.

Galvanizing, 61-66.

Golden varnish for metal, 51.

Green japan grounds, 10.

---- pigment, 46.

Ground, red japan, 10.

---- scarlet japan, 9.

---- tortoise-shell, 12.

Grounds, black, 11.

---- black japan, 12.

---- blue japan, 9.

---- bright pale yellow, 10.

---- green japan, 10.

---- japan, 6-19.

---- orange-coloured, 11.

---- purple, 11.

---- white japan, 7

H

Heating stoves by direct fire, 34.

---- ---- by hot-water pipes, 36.

Hern's process in tin-plating, 60.

I

Immersion process in tin-plating, 59.

Iron, black stain for, 53.

---- galvanized, painting on, 49.

Ironwork, varnishes for, 55.

J

Japan, brown, 57.

---- ground, red, 10.

---- ---- scarlet, 9.

---- ---- grounds, 6-19.

---- ---- black, 12.

---- ---- blue, 9.

---- ---- green, 10.

---- ---- white, 7.

---- work, painting, 13.

---- ---- varnishing, 17.

Japanese gold size, 14.

Japanese lacquer, 47.

Japanning and enamelling stoves, 34.

---- ---- ---- ---- heated by direct fire, 34.

---- ---- ---- ---- heated by hot-water pipes, 36.

---- leather without a priming, first stage, 5.

---- or enamelling metals, 20-28.

---- tin, 25.

---- wood, first stage, 5.

L

Lacquer, Japanese, 47.

M

Metal, golden varnish for, 51.

---- polishes, 51.

Metals, japanning or enamelling, 20-28.

Modern japanning and enamelling stoves, 34.

N

Natural Japanese lacquer, 47.

---- lacquer, 45.

O

Oil vehicle, 14.

Old work, enamelling, 27.

Orange-coloured grounds, 11.

P

Painting japan work, 13.

---- on galvanized iron, 49.

---- ---- zinc, 49.

Paints, black, 52.

Pigments suitable for japanning with natural lacquer, 45.

---- black, 46.

---- blue, 46.

---- green, 46.

---- red, 46.

---- white, 45.

---- yellow, 46.

Polished brass, colours for, 49.

Preparing the surface to be japanned, 4.

Priming the surface to be japanned, 4.

Processes for tin-plating, 58.

Purple grounds, 11.

R

Red japan ground, 10.

---- pigments, 46.

S

Scarlet japan ground, 9.

Sewing machines, black varnish for, 56.

Shellac varnish, 6.

Stoves, modern japanning and enamelling, 34.

Stove, the enamelling and japanning, 29-45.

Surface to be japanned, priming or preparing the, 4.

T

Tin, japanning, 25.

Tin-plating, colours for, 58.

Tin-plating, amalgam process, 59.

---- battery process, 59.

---- Hern's process, 60.

---- immersion process, 59.

---- Weigler's process, 60.

Tortoise-shell ground, 12.

U

Urushiol, 47.

V

Varnish, carriage, 51,

---- for iron and steel, 57.

---- for metal, golden, 51.

---- shellac, 6.

Varnishes for iron work, 55.

Varnishing japan work, 17.

W

Weigler's process of tin-plating, 60.

White japan grounds, 7.

---- pigments, 45.

Wood, first stage in the japanning of, 5.

Y

Yellow grounds, bright pale, 10.

---- pigments, 46.

Z

Zinc, painting on, 49.

ABERDEEN: THE UNIVERSITY PRESS

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ENAMELS AND ENAMELLING

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Handbook on Japanning: 2nd Edition For Ironware, Tinware, Wood, Etc. With Sections on Tinplating and Galvanizing · 第 7 / 7 章