CHAPTER XVI

STRUCTURAL STEEL PAINT TESTS

=The Necessity of Protective Coatings.= Most painters have in the past

considered of minor importance the painting of iron and steel; any paint

that would properly hide the surface of the metal being accepted without

much question. The demand, however, for structural steel for office

buildings, factories, steel cars, railroad equipment, etc., has doubled

the output of structural paints, and created a demand for painters

having a knowledge of the proper materials to use in the painting of

steel, so that its life may be preserved, and its strength maintained.

Such knowledge is as important to the painter as a knowledge of how to

properly select materials for the painting of wood, and how to temper

these materials to suit the various conditions met with.

=The Cause of Rust.= Everyone is familiar with the appearance of rust,

but few actually understand what causes rust. No attempt will be made

here to present even an outline of the many theories advanced to explain

the phenomenon of the rusting of iron, for the subject is as diverse as

it is interesting. A brief resume, however, will be given of the now

generally accepted theory that explains the subject. This theory is

called the electrolytic theory. "Auto-electrolysis" is the term used to

define the peculiar tendency of iron to be transformed from a metal

possessing a hard lustrous surface, high tensile strength, and other

useful properties, to a crumbling oxide that falls to the ground and

again becomes part of the earth from which it was originally taken by

man.

[Illustration: A Side View of Steel Test Fences]

This "going back to nature" is more readily accomplished by most of the

steel produced to-day than by the old hand-made irons produced many

years ago. It seems to be a curious fact that the more quickly a product

or an article is fashioned by man, the more quickly it tends to return

again to its original oxidized condition. Some manufacturers of steel,

however, through an understanding of the causes of rust, have progressed

in the manufacture of slow rusting materials, either by the elimination,

or by the proper distribution of impurities.

When iron is brought into contact with moisture, currents of electricity

flow over the surface of the iron between points that are relatively

pure and points that contain impurities. These currents stimulate the

natural tendency of the iron to go into solution, and the solution

proceeds with vigor at the positive points. The air which the water

contains oxidizes the iron which has gone into solution, and

precipitates the familiar brown iron rust. Thus water, which acts as an

acid, and air, which acts as an oxidizer, have combined together to

accomplish the downfall of the metal.

[Illustration: Three Photomicrographs of Corroding Steel]

=Inhibition and Stimulation of Rust.= It is obvious that if means could

be devised to stop the solution pressure of iron and make it resistant

to the flow of surface electric currents, rust could be prevented. Such

methods have been devised, and to better illustrate how they operate, an

analogy may be drawn between iron in water and shellac in alcohol.

It is common knowledge that when shellac is placed in alcohol, the

shellac will force itself into solution in the alcohol, and form a

clear, transparent lacquer. If, however, there should be mixed with the

alcohol a quantity of water, it would be found that the shellac could no

longer go into solution, and it would remain in its original condition.

In the same way, if there be placed in water a small quantity of

material, such as soluble chromates, or an alkaline substance like

caustic soda or lime, it will be found that iron will no longer have a

tendency to go into solution in this treated water, but will stay bright

and clean. These materials which prevent the rusting of iron have been

called by Cushman, who first advanced these explanations, "rust

inhibitors," or materials which inhibit rusting. The paint maker,

realizing the importance of these rust inhibitors, is incorporating them

into paints designed for the protection of iron and steel, and the

success which paints of this type have met with from a practical

standpoint is a justification of what was first called the "electrolytic

theory," which suggested their use.

By placing small, brightly polished steel plates into a mush of paint

pigment and water, a determination may be made of the pigment's effect

upon the metal. Some pigments, under such conditions, cause rapid

corrosion of the steel plates. Such pigments are stimulators of

corrosion, on account of acid impurities which they contain, or because

of their effect in stimulating galvanic currents. Many carbonaceous

pigments are of this type. Other pigments have the effect of keeping

bright the steel plates and preventing rust. Such pigments are of the

inhibitive type, and their action is to check or retard the solution

pressure of the iron.

=The Effects of Moisture.= It might occur to the reader that although

paint pigments, when mixed up with water and brought into contact with

the surface of steel, might show either an inhibitive or stimulative

action, that it is by no means certain that the same tendency will be

exhibited by pigments when they are properly mixed with linseed oil and

laid out as a film upon the surface of steel. In answer to this, it may

be well to state that almost no material used by mankind is absolutely

dry. Linseed oil, as it is pressed from the seed, comes from the cells,

carrying with it a certain small definite percentage of water, and it is

quite certain that even the best linseed oil that goes into use is not

theoretically dry. Everyone knows, of course, that oil and water do not

readily mix and are, in fact, more or less repellent to each other. It

is, however, true that, in spite of this, oils can carry quite a

percentage of water, without the admixture being apparent to the eye. In

addition to this, careful experiments have proved very conclusively that

linseed oil films, even after they have oxidized and hardened, have the

power to a certain extent of absorbing water from the atmosphere. It is,

therefore, safe to say that no linseed oil film in a paint coating is

dry all the time. As a matter of fact, there is abundant evidence to

show that in rainy weather, and, in fact, when the humidity in the air

is high, paint films have absorbed water. As the sun comes out and warms

the paint coating, and the humidity content of the atmosphere falls,

this water to a large extent evaporates out of the film, only to be

taken up again when the weather conditions change. This action may be

likened to a breathing of the paint film, that is to say, an indrawing

of water under humid conditions, followed by an exhaling of water under

dry conditions. With these facts in mind, it must be apparent that

pigments laid out in intimate contact with the surface of steel are

subjected at all times either more or less to the reactions produced by

water contact. Furthermore, as it is a property of water to become

saturated with the gases of the atmosphere, such as oxygen, carbonic and

sulphurous acids, and other impurities, there is present in a protective

paint film at all times the elements necessary to carry on the corrosive

process and reactions.

An outline of Cushman's original research work, upon which has been

based the classification of pigments as inhibitors, stimulators, and

inerts, is clearly presented in his report[38] as Chairman of Committee

U of the American Society for Testing Materials, of which the following

is an excerpt:

[38] Page 73, 1910 Proceedings of the American Society for Testing

Materials.

[Illustration: Ferroxyl Tests on Painted Steel Surfaces. Upper Row

Painted with Stimulative Paints--Lower Row with Inhibitive Paints.]

[Illustration: Water Test on Plates Painted--Except in Center Spot. Left

Hand Plates Painted with Stimulative Paints, Right Hand Plates Painted

with Inhibitive Paints.]

[Illustration: View of Steel Plates Painted with Stimulative Paints,

after Immersion in Ferroxyl Jelly.]

"Three years ago the suggestion was made in a paper presented before the

Tenth Annual Meeting of this Society that the various types of

substances used as pigments in protective coatings might exert a

stimulative or an inhibitive action on the rate and tendency to

corrosion of the underlying metal. It was further suggested on a

theoretical ground that slightly soluble chromates should exert a

protective action when employed as pigments by maintaining the surface

of the iron in a passive condition in case water and oxygen penetrated

the paint film. In view also of the well-known fact that alkalies

inhibit while acids stimulate the corrosion of iron, it was suggested

that the action of more or less pure pigments on iron in the presence of

water should be thoroughly investigated. Two years ago this Committee

invited the co-operation of Committee D-1 (then known as Committee E) in

the investigation, and a special sub-committee representing the two main

committees was appointed.

"The methods and results of the water-pigment tests have previously been

reported and published, and need not be given in detail. Briefly, the

method consisted in immersing samples of steel in water suspensions of

the various pigments and blowing air through the containers for definite

periods of time, the corrosion being measured by the loss in weight

sustained by the test pieces. About fifty pigments which are in more or

less common use for painting steel were purchased in the open market and

distributed among a number of the members of the Committee, who agreed

to carry out the work. Each investigator worked independently of the

others, except that the same general method was followed; the time of

exposure to the corroding action, however, varied in the different

experiments. When the results were compared and analyzed by the

sub-committee, it was felt that the general agreement of the results

obtained by the several investigators was striking and merited further

and more systematic work. As a result of these tests the sub-committee

tentatively divided the pigments into inhibitors, stimulators, and

indeterminates. The word 'indeterminate' was selected after considerable

discussion, because the words 'neutral' or 'inert' already possess a

special meaning as applied to paint technology. The Committee takes this

occasion to emphatically state that in adopting this tentative

classification, the words 'inhibitive' and 'stimulative' as used by them

up to the present time apply only to the results obtained in the water

tests, and the inference that the results obtained have decided which

class the pigment will fall into when made into a paint with the usual

vehicles and used as a protective coating on iron and steel, is not

justified. In order to make this point quite clear, it has been agreed

by the Committee to qualify the classification so as to speak of the

various materials tested as 'water stimulative' or 'water inhibitive.'"

[Illustration: Apparatus for Testing the Inhibitive Value of Pigments]

=Importance of Field Tests.= Although the laboratory accelerated tests

for the determination of the relative value of structural steel paints

afford information of some import, there seems to be a general opinion

that the best method to follow, if information of a reliable character

is to be obtained, is to make actual field exposure tests upon large

surfaces. The results of the above described water-pigment tests

suggested the erection of a series of steel panels on which to test out

the same pigments under practical service conditions. The Paint

Manufacturers' Association of the United States erected and painted the

panels, the work being under the constant supervision of the writer, and

the inspection of the work under Committee U of the American Society for

Testing Materials. A brief resume of the work[39] is herewith presented.

[39] Page 181, "Corrosion and Preservation of Iron and Steel"--Cushman

and Gardner--McGraw-Hill Book Co., New York City.

=Pickling and Preparation of Plates.= The three types of metal[40]

selected for the test were rolled to billets, the middle of which were

selected, and worked up into plates 24 inches wide, 36 inches high, and

1/8 inch in diameter--approximately 11 gauge. A number of plates of each

of the metals selected, in all 450, were pickled in 10% sulphuric acid,

kept at 180 to 200 degrees Fahrenheit, in order to remove the

mill-scale. The plates were then washed in water, and later in 10%

solution of caustic soda. Finally the plates were again washed in water

and wiped dry. They were then packed in boxes containing dry lime, in

order to prevent superficial corrosion. By this method the plates were

secured in perfect condition, the surfaces being smooth and free from

scale. Upon these pickled plates paints were applied with a definite

spreading rate of 900 square feet per gallon. The unpickled plates,

coated with mill-scale, were painted with the same paints, but without

adopting any special spreading rate, thus following more closely the

ordinary method of painting structural steel. A few extra plates of

special Bessemer steel and Swedish charcoal iron were also included in

the test, some of which were painted, while others were exposed without

any protective coating. Plates of the three types of metal already

mentioned were also exposed unpainted, both in the black and pickled

condition.

[40] Bessemer Steel, Open Hearth Steel, and Pure Iron.

[Illustration: Front View of Steel Test Fences]

=Fence Erection and Preparation for Work.= The fences which were erected

for the holding of the plates were constructed of yellow pine, the posts

being set deeply in the ground and properly braced. The framework of the

fence was open, with a ledge upon the lateral girders, upon which the

plates might rest, and to which the plates were secured by the use of

steel buttons. After the framework had been erected, painted, and made

ready for the placement of the panels, a small shed was built upon the

ground, and the materials for the field test placed therein. The steel

plates were unpacked from the boxes in which they were shipped, brushed

off, and stacked up ready for painting. Small benches were erected, and

the accessories of the work, such as cans, brushes, pots, balances,

etc., were placed in position.

=Methods Followed in Painting Plates.= A frame resting upon the

workbench served to hold the plates in a lateral position while being

painted, room being allowed beneath the plate for the operator to place

his hands in order to lift the plates from the under surface after the

painting had been finished.

A pickled plate having been placed upon the framework everything was in

readiness for the work. The specific gravity and weight per gallon of

the paint to be applied was determined, and the amount, in grams, to be

applied to each individual panel was calculated according to the

following formula:

Spreading rate Sq. ft. in plate Grams paint in gal.

900 sq. ft. : 6 :: 5400 : x

The reciprocal of _x_ being the number of grams of paint to be applied

to the panels.

An enamel cup was then filled with the paint and a brush well stirred

within. The cup, paint, and brush were placed upon the balances and

accurately weighed in grams. After most of the paint had been applied to

the panel, cross-brushing of the panel was continued until the pot with

brush and paint exactly counterbalanced the deducted weight. The painted

panel was then set in a rack, in a horizontal position to dry.

A period of eight days elapsed between the drying of each coat. The

greatest care was taken in the painting of the edges of the plates, and

the racks for containing the plates after they were painted were so

constructed that the paint would not be abraded while sliding the plates

back and forth. The working properties of each paint, and the appearance

of the surface of each plate after painting, were carefully noted and

included in the report. No reductions were made to any of the paints

applied except in three cases, where the viscosity was so great that it

was necessary to add a small amount of pure spirits of turpentine. The

amount of paint was proportionately increased in such cases, so that the

evaporation of the turpentine would leave upon the plate the amount of

paint originally intended.

The appearance of the completed series of test panels is shown on page

221.

=Vehicles Used and Reasons for Avoidance of Japan Driers.= The pigments

used were selected with the view to securing as nearly as possible

purity and strength, and as already noted, were out of the same lots

used in making the preliminary laboratory tests on inhibitives. They

were ground in a vehicle composed of two parts of raw linseed oil and

one part of pure boiled oil. Paint is generally caused to dry rapidly by

the use of japan or driers. These materials contain a large amount of

metallic oxides which might have some effect in either exciting or

retarding corrosion. To prevent the introduction of such a factor, these

materials were not used in the test. The boiled oil, with its small

percentages of metallic oxides, was sufficient, however, to cause the

paints to dry in a short time after they were spread.

=Testing Effect of Various Prime Coats.= Some of the special tests made

included a series of plates prime-coated with different inhibitive

pigments, and these tests were designed to determine which pigments

offer the best results for such work. These plates were all

second-coated with the same paint. It is the opinion of the authors that

any good excluding paint may be used whether it be inhibitive in action

or not, provided the contact coat is inhibitive. If, however, both coats

can be designed so as to have the maximum possible value from both these

points of view, the best results would, of course, accrue. The only way

such data can be obtained is by careful observation of the results of

exposure tests.

=Combination Formulas Tested.= By selecting a series of pigments which

in the water tests showed inhibitive tendencies, and properly combining

these pigments into a paint, it was thought possible that a more or less

inhibitive paint would be produced. If this proved to be the case, it

would follow that the selection and introduction into a paint of the

stimulative pigments would inevitably produce a paint unfit for use on

iron or steel.

=Data on Application of Paints.= The recorded data on the application of

the paint to the panels is voluminous. There is presented herewith,

however, the data on two of the paints.

NO. 2, QUICK PROCESS WHITE LEAD:

Sp. Gr. of pigment 6.78

Lbs. to gallon oil 20.34

Sp. Gr. of paint as received 2.47

Wt. of paint per gallon 20.56

Grams to panel 62

Condition of paint Good

Working properties Works easy

Drying 24 hrs. all coats

1 coat Oct. 26 T 60 B 29.94 W. fair

2 coat Nov. 3 T 54 B 30.23 W. clear

3 coat Nov. 7 T 52 B 29.66 W. cloudy

NO. 9, ORANGE MINERAL (AMERICAN):

Sp. Gr. of pigment 8.97

Lbs. to gallon oil 26.91

Sp. Gr. of paint as received 2.97

Wt. of paint per gallon 24.74

Grams to panel 74.7

Condition of paint Good

Working properties Smooth--no brush marks

Drying Good

1 coat Oct. 28 T 58 B 30.01 W. cloudy

2 coat Nov. 4 T 65 B 29.61 W. cloudy

3 coat Nov. 9 T 58 B 29.91 W. clear

=Composition of Paints.= The following table gives data regarding the

composition, etc., of paints applied to the steel panels.

=Results of Inspection.= The results of an inspection of the steel test

plates, made by Sub-committee D representing Committee D-1 of the

American Society for Testing Materials, is herewith presented:

"On Wednesday, June 28, 1911, the second inspection of the Atlantic City

Steel Test Panels, erected in October, 1908, was made by Sub-committee D

of Committee D-1, this Committee having agreed to report upon the

condition of the painted surfaces, leaving any report on the comparative

corrosion of the various types of metal used in the test to Committee

A-5 on the corrosion of iron.

===+=========================+=======+=======+======+=======+=========

| | | | | |Grams

| | | | | |Paint

| | |Wt. of | Sp. |Wt. of |to Panel

| Name | Sp. |Pigment| Gr. | Paint |at 900

| | Gr. |to Gal.| of | per |Sq. ft.

Pigment |of Pig-|of oil |Paint | Gal. |spreading

No.| | ment | Lbs. |Rec'd | Lbs. |rate

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

1|Dutch process white lead | 6.83 | 20.49 | 2.45 | 20.49 | 61.0

2|Quick process white lead | 6.78 | 20.34 | 2.47 | 20.34 | 62.0

3|Zinc oxide | 5.56 | 16.68 | 2.12 | 16.68 | 59.0

4|Sublimed white lead | 6.45 | 19.17 | 2.36 | 19.17 | 59.0

5|Sublimed blue lead | 6.39 | 19.17 | 2.42 | 19.17 | 61.0

6|Lithopone | 4.26 | 12.78 | 1.80 | 12.78 | 45.3

7|Zinc lead white | 4.42 | 13.26 | 1.96 | 13.26 | 49.4

9|American orange mineral | 8.97 | 26.91 | 2.97 | 26.91 | 74.7

10|Red lead | 8.70 | 26.10 | 2.93 | 26.10 | 73.6

12|Bright red oxide | 5.26 | 15.78 | 2.05 | 15.78 | 60.0

14|Venetian red | 3.1 | 9.30 | 1.52 | 9.30 | 38.0

15|Prince's metallic brown | 3.17 | 9.51 | 1.50 | 9.51 | 37.7

16|Natural graphite | 2.60 | 7.80 | 1.37 | 7.80 | 34.4

17|Acheson graphite | 2.21 | 6.63 | 1.22 | 6.63 | 30.8

19| {Lampblack | | 1.82}| | 1.82 |

| {Barytes | 1.82 | 8.92}| 1.60 | 8.92 | 40.2

20|Willow charcoal | 1.49 | 4.47 | 1.08 | 4.47 | 27.0

21| {Gas carbon black | 1.85 | 1.39}| 1.67 | 1.39 |

| {Natural barytes | | 10.03}| | 10.03 | 50.7

24|French yellow ochre | 2.94 | 8.82 | 1.46 | 8.82 | 37.0

27|Natural barytes | 4.46 | 13.38 | 1.83 | 13.38 | 46.0

28|Precipitated barytes | 4.23 | 12.69 | 1.84 | 12.69 | 46.0

|(blanc fixe) | | | | |

29|Calcium carbonate | 5.48 | 8.22 | 1.37 | 8.22 | 34.5

|(whiting) | | | | |

30|Calcium carbonate | 2.56 | 7.68 | 1.35 | 7.68 | 34.0

|precipitated | | | | |

31|Calcium sulphate (gypsum)| 2.33 | 6.99 | 1.25 | 6.99 | 31.4

32|China clay (kaolin) | 2.67 | 8.01 | 1.34 | 8.01 | 34.0

33|Asbestine (silicate of | 2.75 | 8.25 | 1.38 | 8.25 | 34.7

|magnesium) | | | | |

34|American vermilion | 6.83 | 20.49 | | 20.49 | 64.5

|(chrome scarlet) | | | | |

36|Medium chrome yellow | 5.88 | 17.64 | | 17.64 | 67.1

39|Zinc chromate | 3.57 | 10.71 | 1.57 | 10.71 | 39.2

40|Zinc and barium chromate | 3.45 | 10.35 | 1.58 | 10.35 | 40.0

41|Chrome green (blue tone) | 4.44 | 13.32 | 1.94 | 13.32 | 49.0

44|Prussian blue | 1.96 | 5.88 | | 5.88 | 30.0

45|Prussian blue | 1.93 | 5.79 | | 5.79 | 34.5

48|Ultramarine blue | 2.40 | 7.20 | 1.29 | 7.20 | 32.5

49|Zinc and lead chromate | 4.76 | 14.28 | 1.92 | 14.28 | 48.3

51|Magnetic black oxide | | 15.00 | 1.92 | 15 | 48.3

| | | | | |

| _Composite Paints_ | | | | |

| | | | | |

111|Brown } Made from pig- | | 10.82 | 1.30 | 10.82 | 32.7

222|Black } ments that were | | 10.86 | 1.30 | 10.86 | 32.8

333|White } inhibitive in the| | 14.52 | 1.74 | 14.52 | 43.8

444|Green } water test | | 12.77 | 1.53 | 12.77 | 38.6

| | | | | |

555|Black } Made from pig- | | 9.37 | 1.125| 9.37 | 28.

666|Brown } ments that were | | 11.74 | 1.41 | 11.74 | 35.5

777|White } stimulative in | | 14.55 | 1.75 | 14.55 | 44.

888|Green } the water test | | 14.57 | 1.75 | 14.57 | 14.57

===+=========================+=======+=======+======+=======+=========

"According to the amount of rust apparent on the painted surfaces of the

panels, as well as the degree of checking, chalking, scaling, cracking,

peeling, loss of color, and other signs of paint failure shown, ratings

were given each panel. The system of rating which took into

consideration all the above conditions, was similar to the system used

at the first inspection during 1910, when 0 (zero) recorded the worst

results and 10 (ten) the best results.

"In Table No. 1 there is shown the rating accorded by each inspector to

each panel, as well as an average for each panel.

TABLE NO. 1.--SECOND INSPECTION OF STEEL PAINT TEST PANELS AT ATLANTIC

CITY, N. J., BY SUB-COMMITTEE D OF COMMITTEE D-1

=======+========================+======+======+=======+=======+=======

| | | | H. A. | |

Panel | |W. H. |P. H. |Gardner| C. |

No. | Pigment |Walker|Walker|Chair- |Chapman|Average

| | | | man | |

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

1 |Dutch process white lead| 2 | 3 | 3 | 5 | 3.7

2 |Quick process white lead| 4 | 4 | 3 | 6 | 4.2

3 |Zinc oxide (XX) | 1 | 1-1/2| 1 | 2-1/2| 1.5

4 |Sublimed white lead | 9 | 9-1/2| 9 | 8-1/2| 9.0

5 |Sublimed blue lead | 9 | 9-1/2| 9-1/2| 7-1/2| 8.8

6 |Lithopone | 2 | 1-1/2| 2 | 3-1/2| 2.2

7 |Zinc lead white | 3 | 4 | 5 | 7 | 4.7

9 |Orange mineral | 9 | 9 | 9 | 6-1/2| 8.3

10 |Red lead | 9 | 9 | 9 | 6-1/2| 8.3

12 |Bright red oxide | 8-1/2| 9 | 8 | 7 | 8.1

14 |Venetian red | 7 | 9 | 7 | 9 | 8.0

15 |Prince's metallic brown | 5 | 7-1/2| 6 | 8 | 6.3

16 |Natural graphite | 6 | 8 | 4 | 9-1/2| 6.8

17 |Artificial graphite | 5 | 7-1/2| 4 | 7 | 5.9

19 |Lampblack | 5 | 7-1/2| 5 | 8 | 6.3

20 |Willow charcoal | 9 | 8-1/2| 9 | 9 | 8.8

21 |Carbon black | 7 | 8-1/2| 5 | 8-1/2| 7.2

24 |Yellow ochre (French) | 5 | 7 | 2 | 8 | 5.5

27 |Barytes (natural) | 1 | 1 | 1 | 0 | 0.7

28 |Barytes (precipitated) | 2 | 1-1/2| 2 | 2 | 1.8

29 |Calcium carbonate | 0 | 0 | 0 | 0 | 0.0

|(whiting) | | | | |

30 |Calcium carbonate (pre- | 0 | 0 | 0 | 0 | 0.0

|cipitated) | | | | |

31 |Calcium sulphate | 1 | 1 | 1 | 3 | 1.7

|(gypsum) | | | | |

32 |China clay (kaolin) | 6 | 6 | 7 | 6-1/2| 6.3

33 |Asbestine (magnes. sili-| 5 | 4-1/2| 6 | 5 | 5.1

|cate) | | | | |

34 |American vermilion |10 |10 | 10 | 10 | 10.0

36 |Lead chromate | 7 | 7-1/2| 8-1/2| 8 | 7.7

39 |Zinc chromate | 9 | 9 | 10 | 9-1/2| 9.5

40 |Zinc and barium chromate| 9 | 9-1/2| 10 | 9-1/2| 9.5

41 |Chrome green (blue tone)|10 |10 | 10 | 9-1/2| 9.8

44 |Prussian blue, W. S | 9 | 9-1/2| 9-1/2| 9 | 9.0

45 |Prussian blue, W. I | 8 | 9-1/2| 8-1/2| 8-1/2| 8.5

48 |Ultramarine blue | 0 | 0 | 0 | 0 | 0.0

49 |Zinc and lead chromate |10 | 9-1/2| 10 | 9-1/2| 9.7

51 |Magnetic black oxide | 9 | 9-1/2| 10 | 9-1/2| 9.5

111 |Brown composite paint | 7 | 9 | 9 | 9 | 8.5

222 |Black composite paint | 9 | 9 | 9 | 8-1/2| 8.8

3333 |White composite paint | 4 | 4 | 7 | 3 | 4.5

444 |Green composite paint | 5 | 7 | 7 | 8 | 6.7

555 |Black composite paint | 9 | 9 | 6 | 9 | 8.2

666 |Brown composite paint | 8 | 8 | 6 | 9 | 7.7

777 |White composite paint | 7 |10 | 5 | 7 | 7.2

888 |Green composite paint | 7 | 8 | 8 | 9 | 8.0

2000 |1 coat zinc chromate }| 8 | 8-1/2| 8 | 8 | 8.1

|1 coat iron oxide ex- }| | | | |

|cluder }| | | | |

3000 |1 coat lead chromate | 7 | 8 | 7 | 7-1/2| 7.3

4000 |1 coat red lead }| 7 | 8-1/2| 8 | 7-1/2| 7.7

|1 coat iron oxide ex- }| | | | |

|cluder }| | | | |

100 |Straight carbon black | 5 | 8-1/2| 4 | 8-1/2| 6.5

|paint with turps and | | | | |

|drier | | | | |

90 |Straight lampblack paint| 5 | 7 | 3 | 8 | 5.7

|with turps and drier | | | | |

5555 |Coal tar paint over red | 4 | 8 | 2 | 7 | 5.2

|lead | | | | |

1000 |Chrome resinate in oil | 1 | 0 | 0 | 2 | 0.7

|(1 coat) | | | | |

1 plate|3 coats boiled linseed | 1 | 0 | 1 | 4 | 1.5

|oil | | | | |

=======+========================+======+======+=======+=======+=======

"In Table No. 2 there is shown the rating obtained by those panels which

were considered by the committee as meriting from 8 to 10, and having

given the best all-round service.

TABLE NO. 2.--ANALYSIS OF AVERAGES. GRADE OF EXCELLENCE FROM 8 TO 10

=====+=============================================+=======

Plate| Pigment |Average

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

34 | American vermilion (basic chromate of lead) | 10.0

41 | Chrome green | 9.8

49 | Lead and zinc chromate | 9.7

39 | Zinc chromate | 9.5

40 | Zinc and barium chromate | 9.5

51 | Black oxide of iron | 9.5

4 | Sublimed white lead | 9.0

44 | Prussian blue | 9.0

5 | Sublimed blue lead | 8.8

20 | Willow charcoal | 8.8

222 | Composite paint | 8.8

45 | Prussian blue | 8.5

111 | Composite formula | 8.5

9 | Orange mineral | 8.3

10 | Red lead | 8.3

555 | Composite paint | 8.2

12 | Bright red oxide of iron | 8.1

2000 | 1 coat zinc chromate; 1 coat iron oxide | 8.1

14 | Venetian red | 8.0

888 | Composite paint | 8.0

=====+=============================================+=======

=Comparison of Results.= It is of interest to compare with Table 2 of

the above report, Table 2 of the 1910 report of Committee U of the

American Society for Testing Materials. Both charts show the highly

inhibitive pigments to be in the lead.

COMMITTEE U REPORT 1910

TABLE II.--ANALYSIS OF AVERAGES. GRADE OF EXCELLENCE FROM 8 TO 10

(_Only resistance to corrosion was considered, and only pigments which

were common to both tests are included_)

===+====================================+=======

No.| Pigment |Average

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

34 | American vermilion (chrome scarlet)| 9.8

41 | Chrome green (blue tone) | 9.7

40 | Zinc and barium chromate | 9.7

5 | Sublimed blue lead | 9.6

4 | Sublimed white lead | 9.5

49 | Zinc and lead chromate | 9.5

39 | Zinc chromate | 9.4

12 | Bright red oxide | 9.3

44 | Prussian blue (water stimulative) | 9.2

16 | Natural graphite | 9.1

9 | Orange mineral (American) | 9.0

36 | Medium chrome yellow | 9.0

2 | White lead (quick process) | 8.9

20 | Willow charcoal | 8.8

45 | Prussian blue (water inhibitive) | 8.8

1 | White lead (Dutch process) | 8.7

10 | Red lead | 8.7

7 | Zinc lead white | 8.0

===+====================================+=======

The writer has recently made a careful inspection of the panels painted

with single pigment paints, and has made the following brief summary of

the characteristic appearance of each.

=Panel No. 1--Dutch Process White Lead.= The excessive chalking which

took place began to disappear at the end of a year, being washed away by

the rains and carried away by the winds, so that there was left upon the

surface but a thin coating of pigment, insufficient to give good

protection. Slight corrosion was apparent beneath the film.

=Panel No. 2--Quick Process White Lead.= In the same condition as Panel

No. 1.

=Panel No. 3--Zinc Oxide.= Panel covered with thin lateral streaks of

rust, due to the admittance of moisture in cracks caused by brittleness

of film. Result doubtless due to insufficient amount of oil used with

pigment. Removal of film shows steel very bright except where cracks

have formed.

=Panel No. 4--Sublimed White Lead.= Although sublimed white lead chalked

very heavily, the chalked pigment seemed to be tenacious and adhered to

the plate, presenting an excellent surface with absence of rust. Film of

good color and quite elastic.

=Panel No. 5--Sublimed Blue Lead.= In same condition as Panel No. 4, but

color has slightly faded.

=Panel No. 6--Lithopones.= Lithopone was early destroyed, as is usual

with this pigment when used alone on exterior surfaces. It became rough

and discolored, presenting a very blotchy appearance and disclosed the

formation of rust working through the film.

=Panel No. 7--Zinc Lead White.= In general good condition with the

exception of the color, which is slightly dark. Medium chalking was

apparent but only very slight corrosion appeared.

=Panel No. 9--Orange Mineral.= In excellent condition, showing a good

firm surface with no checking or corrosion apparent. Shortly after

exposure the film became covered with a white coating of carbonate of

lead, which indicates action of the red lead with the carbonic acid of

the atmosphere. Removal of this white coating with water discloses the

brilliant color of the unaffected portion of the red lead.

=Panel No. 10--Red Lead.= In same condition as Panel No. 9.

=Panel No. 12--Bright Red Iron Oxide.= In general good condition. Film

intact and unfading in color.

=Panel No. 14--Venetian Red.= Similar to Panel No. 12, but slight

corrosion apparent beneath, in localized spots, and film showing slight

wart-like formations.

=Panel No. 15--Prince's Metallic Brown.= Similar to Panel No. 14.

=Panel No. 16--Natural Graphite.= Deeply pitted in spots, showing

bulbous eruptions, indicating the stimulative nature of this pigment.

=Panel No. 17--Artificial Graphite.= In same condition as Panel No. 16.

=Panel No. 19--Lampblack and Barytes.= Although the film seems to be

intact, there are apparent abrasions of the surface showing stimulative

corrosion effects of a pronounced nature.

=Panel No. 21--Carbon Black and Barytes.= In same condition as Panel No.

19.

[Illustration: Corrosion Pits on Graphite Panel]

[Illustration: Rust on Stripped Graphite Film]

[Illustration: Section of Wire Painted with a Stimulative Carbonaceous

Paint]

[Illustration: Corroded and Pitted Surface of Plate Painted with

Stimulative Paint]

The longevity of lampblack and carbon black paint films when applied to

wood has been attributed to the slow drying nature of these pigments

when mixed with oil. It is assumed that they have the property of

keeping the oil in a semi-drying condition, which will not disintegrate

as early as when the oil is thoroughly dried to linoxyn. If this is

true, it would seem advisable to use with hard-drying pigments, a

proportion of some oil that is semi-drying in nature or one which will

leave a film not too hard. Soya bean oil, wood oil, and fish oil present

themselves as candidates for such use. How they will work in practice,

however, is a question not yet determined. On the other hand, it is well

known that these pigments require enormous quantities of oil in order to

grind to a working consistency, and it is possible that the life of

such coatings is due rather to the property of these pigments, of taking

up large quantities of oil, than to their effect upon the slow drying of

oil. Excessive oil carrying, however, should be avoided, as shown by the

early failure and pitting of those carbon black and lampblack paints

ground with very large quantities of oil, as is the usual practice. When

these carbon and lampblack pigments were ground with barytes (which is a

heavy pigment and requires only about 9 pounds of oil to 100 pounds of

pigment, as against 175 pounds of oil to 100 pounds of lampblack), it

was found that the lampblack and carbon black paints were reinforced and

made more suitable for actual practice. The stimulative nature of these

black pigments, however, asserted itself in both cases, and large

pittings and eruptions were evident at the end of a year. Carbon black,

lampblack, graphite, or any other good conductor of electricity should

never be placed next to the surface of iron. They are good as

top-coatings, but not as prime-coaters. Some pigments are stimulators of

corrosion, because they contain water-soluble impurities that hasten the

rusting, while others, like graphite, hasten it simply because, being

good conductors, they stimulate surface electrolysis.

=Panel No. 20--Willow Charcoal.= In excellent condition throughout.

Presence of small quantities of potash may be responsible for the

inhibitive nature of this black pigment.

=Panel No. 24--Ochre.= While the film seems intact, it has a very

mottled appearance and examination shows eruptions of rust through the

film, in several places.

=Panel No. 27--Natural Barytes.= Within a year the film became

pin-holed, and corrosion was apparent. At the end of three years very

little of the pigment was left upon the plate, having chalked and scaled

off. Barytes has proved its usefulness as a constituent of a combination

type of paint, but it should not be used alone.

=Panel No. 28--Blanc Fixe.= In the same condition as Panel No. 27, but

slightly more chalking and disintegration was shown.

[Illustration: Panel Painted with Blanc Fixe. Right Side Stripped of

Paint to Show Corrosion]

[Illustration: Scaled Whiting Films

Chemically Active Pigments and Their Effect After Eighteen Months'

Wear]

[Illustration: Plate Showing Effect of Chemically Active Pigments on Oil

after One Year's Wear]

=Panel No. 29--Whiting.= Plates coated with calcium carbonate or whiting

in oil presented a very fair appearance at the start of the test, but

they soon began to chalk and disintegrate. It is well known that

whiting, being alkaline, has the property of acting on oil and causing

its early disintegration by saponification. As a matter of fact, six

months after the whiting plates were exposed, crumbling of the surface

appeared, and twelve months was sufficient for the total destruction of

the paint. At this time the rusted surface of the plates which had been

painted with calcium carbonate, seemed not to rust as fast as those

plates which were exposed without paint coatings, and the rust which had

formed appeared to be of an even, fine texture. On the lower left-hand

corner of these plates had been lettered the figures "29" and "30,"

using lampblack in oil. One of the most remarkable things which appears

on the fence to-day is the perfect condition of these lampblack letters

over their priming coat of calcium carbonate, standing out in clear

relief against the rusted metal. This test would suggest, therefore,

that if the surface of metal is properly protected with a pigment which

is slightly alkaline or inhibitive in nature, and then topped with a

good weather-resisting material, such as lampblack, graphite or carbon

black, good results would be obtained. Further tests will be made to

determine the value of this suggestion.

=Panel No. 30--Precipitated Calcium Carbonate.= Showed more rapid

destruction than Panel No. 29.

[Illustration: Corrosion Adhering to Film Stripped from Panel Painted

with Gypsum (Calcium Sulphate)]

=Panel No. 31--Calcium Sulphate.= Under the paint film of gypsum, rust

soon appeared, showing that the film was not a good excluder of

moisture. Although the film remained intact, rusting progressed

throughout the test and considerably darkened the color of the paint.

=Panel No. 32--China Clay.= This pigment gave excellent service for

eighteen months. Afterwards indications of corrosion were shown, and

apparent breakdown of the film was indicated.

[Illustration: China Clay

Asbestine

Gypsum]

=Panel No. 33--Asbestine.= In the same condition as Panel No. 32.

[Illustration: Excellent Surface shown by American Vermilion after

nearly Four Years' Exposure]

=Panel No. 34--American Vermilion.= This pigment has given perfect

protection to the plates. The film is strong and elastic, and upon

removal reveals the bright steel. No chalking, checking, discoloration,

or other signs of paint failure are shown. It would appear that the

inhibitive characteristics of this pigment are pronounced, and it

promises to give efficient service for several years more.

=Panel No. 36--Lead Chromate.= This panel is in generally fair

condition, but slight checking is shown.

[Illustration: Perfect Condition of Plate Painted with Zinc Chromate;

One Half Stripped. (_Negative cracked_)]

=Panel No. 39--Zinc Chromate.= This panel is in condition similar to

Panel No. 34, presenting a perfect appearance, with decided maintenance

of color, elasticity of film, and freedom from any bad characteristics.

It has proved to be one of the highest type rust inhibitive pigments.

=Panel No. 40--Zinc-and-Barium-Chromate.= Although the color of this

pigment is not very pleasing, it has proved itself to be the equal of

zinc chromate in its protective value.

=Panel No. 41--Chrome Green.= In excellent condition. Presents an

appearance similar to Panels Nos. 34 and 39. Its surface is perfect and

will doubtless give service for many years.

=Panel No. 44--Prussian Blue.= This panel stands forth as the most

wonderful moisture-excluder in the whole test, its surface presenting an

appearance similar to a varnished plate, even after three years'

exposure. Action between the pigment and the oil, resulting in the

formation of iron linoleate, may account for this property.

=Panel No. 45--Prussian Blue.= In same condition as Panel No. 44.

=Panel No. 48--Ultramarine Blue.= Soon after this test was exposed,

early vehicle decay and excessive chalking were observed. The admittance

of moisture may have caused the formation of acid with the sulphur

content of the pigment, which would account for the rapid corrosion

which followed. It is of a pronounced stimulative type. The effect of

stimulative under-coatings is well shown on some special plates on the

fence, which when received were not pickled before painting, but had

upon their surfaces the ordinary coating of mill scale. Over this had

been stencilled in a triangular form the trade mark of the manufacturer.

The stencilling material was made of ultramarine blue. When these plates

were painted with some of the special paints, and exposed, the

stimulative nature of the ultramarine blue began to assert itself, and

within a short time, wherever the stencil marks were located, signs of

rust began to appear through the coatings of top paint which had been

applied. Corrosion under these stencil marks became so great that the

trade mark was plainly outlined in letters of rust. This would seem to

be final proof that pigments of a stimulative nature should never be

used for the priming of iron and steel.

=Panel No. 49--Zinc-Lead Chromate.= In excellent condition throughout,

with a smooth surface and showing no corrosion. Stands in the same class

as Panels Nos. 34 and 39.

[Illustration: Effect of Stimulative Paint. Manufacturer's Trade Mark

Stencilled on Bare Metal in Triangular Form, showing Through Subsequent

Paint Coating]

=Panel No. 51--Black Magnetic Oxide of Iron.= In excellent condition.

Paint Technology and Tests · 第 16 / 17 章