Albertalates Albert Products, Ltd., Erith, Kent.

Dulux Nobel Chemical Finishes Ltd., London.

Glyptal British Thompson Houston Co., Ltd., Rugby.

Micanite Micanite and Insulators Co., Ltd., Walthamstow,

London.

Paralac Imperial Chemical Industries, Ltd., London.

Acrylate resins:

Diakon and Perspex Mouldrite Ltd., Division of Imperial Chemical

Industries, Ltd., London.

Aniline resins:

Panilax Micanite and Insulators Co., Ltd., London.

APPENDIX D

TRADE NAMES FOR SYNTHETIC RESINS MADE IN GERMANY

_Trade name_ _Maker_

Tar-acid resins:

Alberid Dr. Kurt Albert G. m. b. H., Chemische Fabrik,

Wiesbaden-Biebrich.

Albertol Dr. Kurt Albert G. m. b. H., Chemische Fabrik,

Wiesbaden-Biebrich.

Ambresit Chemische Fabrik Ambra, Zittau i. Sachsen (in

liquidation).

Ammoplaste I. G. Farbenindustrie A. G., Frankfort-on-Main.

Backdura Bakelite G. m. b. H., Berlin.

Bakelit Bakelite G. m. b. H., Berlin.

Bakelit A (Resol) Bakelite G. m. b. H., Berlin.

Bakelit C Bakelite G. m. b. H., Berlin.

Bezet Harz Louis Blumen, Zwickau i. Sachsen.

Boschbakelite Robert Bosch A. G., Stuttgart.

Celloresen Louis Blumer, Zwickau i. Sachsen.

Dekorit Dr. F. Raschig G. m. b. H., Ludwigshafen a.

Rhein.

Durax

Durophen Dr. Kurt Albert G. m. b. H., Wiesbaden-Biebrich.

Elastolith Herold A. G., Hamburg 33.

Ethyl cellulose I. G. Farbenindustrie A. G., Frankfort-on-Main.

Faturan Dr. Heinr. Traun & Sohne, Hamburg.

Ferrozell Deutsche Ferrozell G. m. b. H., Augsburg.

Greif Faturan Dr. H. Traun & Sohne, Hamburg.

Havegit Saureschutz G. m. b. H., Berlin.

Herolith Herold A. G., Hamburg.

Hornolith Hornolith G. m b. H., Berlin S 59.

Ivorax Herold A. G., Hamburg.

Koraton Wedig & Reu.

Kunstharz 26 Z I. G. Farbenindustrie A. G., Frankfort-on-Main.

Laccain Louis Blumer, Zwickau i. Sachsen.

Leukorit Dr. F. Raschig G. m. b. H., Ludwigshafen a.

Rhein.

Lithocorn A. Elhardt Sohne, Kempten, Bayern.

Marbolith Herold A. G., Hamburg 33.

Metakalin I. G. Farbenindustrie A. G., Frankfort-on-Main.

Neoresit August Nowak A. G., Bautzen.

Novolack Bakelite G. m. b. H., Berlin.

Novotext Allgemeine Elektrizitats-Gesellschaft, Berlin.

Ornalith Herold A. G., Hamburg

Phenolplaste I. G. Farbenindustrie A. G., Frankfort-on-Main.

Redmanol (Bakelit A) Bakelite G. m. b. H., Berlin.

Resenoplast Louis Blumer, Zwickau i. Sachsen.

Resinit Bakelite G. m. b. H., Berlin.

Resinole Dr. F. Raschig G. m. b. H., Ludwigshafen a.

Rhein.

Resit Bakelite G. m. b. H., Berlin.

Resol Bakelite G. m. b. H., Berlin.

Schellackersatz I. G. Farbenindustrie A. G., Frankfort-on-Main.

Dr. A. Wacker Gesellschaft für Elektrochemische

Industrie G. m. b. H., München.

Dr. Kurt Albert, Wiesbaden-Biebrich.

Sipilite Bakelite G. m. b. H., Berlin.

Supraresen Louis Blumer, Zwickau i. Sachsen.

Syntellac Dr. A. Wacker G. m. b. H., München.

Tenazit Allgemeine Elektrizitats-Gesellschaft, Berlin.

Toplast Louis Blumer, Zwickau i. Sachsen.

Trolon Rheinisch-Westfalische Sprengstoff Fabriken,

Troisdorf.

Turbax Jaroslaw’s Erste Glimmerwarenfabrik, Berlin

SO 36.

Vigorith Dr. F. Raschig, Ludwigshafen a. Rhein.

Vinnapas Dr. A. Wacker G. m. b. H., München.

Wackerschellack Dr. A. Wacker G. m. b. H., München.

Wenjazit Kunst-Rohstoff A. G., Hamburg-Einbeck.

Alkyd resins:

Alftalate Dr. Kurt Albert G. m. b. H., Chemische Fabrik,

Wiesbaden-Biebrich.

Alkydal I. G. Farbenindustrie A. G., Frankfort-on-Main.

Beckacite Beckacite Kunstharzfabrik, G. m. b. H.,

Hamburg-Wandsbeck.

Beckosol Beckacite Kunstharzfabrik, G. m. b. H.,

Hamburg-Wandsbeck.

Duxol Louis Blumer, Zwickau i. Sachsen.

Duxalid Louis Blumer, Zwickau i. Sachsen.

Geaphthal Allgemeine Elektrizitats-Gesellschaft, Berlin.

Glyptal Dr. Kurt Albert G. m. b. H., Wiesbaden-Biebrich.

Urea resins:

Hares L H. Rommler A. G., Berlin W 62.

Locron I. G. Farbenindustrie, A. G., Frankfort-on-Main.

Pluviusin Kunstharzfabrik Dr. F. Pollack, Vienna, German

branch Berlin.

Pollopas Rheinisch-Westfalische Sprengstoff Fabriken,

Troisdorf, Bez. Koln.

Vinyl resins:

Acronal I. G. Farbenindustrie, A. G., Frankfort-on-Main.

Mowilith I. G. Farbenindustrie, A. G., Frankfort-on-Main.

Polystyrene resins:

Metastyrol I. G. Farbenindustrie, A. G., Frankfort-on-Main.

Mollit I. G. Farbenindustrie, A. G., Frankfort-on-Main.

Trolitul Rheinisch-Westfalische Sprengstoff Fabriken,

Troisdorf.

Acrylate resins:

Plexigum Rohm & Haas, Darmstadt.

Other resins:

Coumarone resins Kokawerke & Chemische Fabriken A. G., Berlin

N. W. 40.

Harz No. 30 Ciba A. G., Berlin-Wilmersdorf.

Harz No. 238 Ciba A. G., Berlin-Wilmersdorf.

Ultrasit Chemische Fabrik Ambra, Zittau, Sachsen, (in

liquidation).

Utilith Deutsche Rohstoffindustrie, Augsburg.

APPENDIX E

LIST OF UNITED STATES MANUFACTURERS OF RAW MATERIALS FOR SYNTHETIC

RESINS[28]

Phenol:

Barrett Co., New York, N. Y.

Calco Chemical Co., Inc., Bound Brook, N. J.

Dow Chemical Co., Midland, Mich.

Koppers Co., Pittsburgh, Pa.

Monsanto Chemical Co., St. Louis, Mo.

Reilly Tar & Chemical Corp., Indianapolis, Ind.

Cresols:

Barrett Co., New York, N. Y.

Calco Chemical Co., Inc., Bound Brook, N. J.

Givaudan-Delawanna, Inc., Delawanna, N. J.

Koppers Co., Pittsburgh, Pa.

Reilly Tar & Chemical Corp., Indianapolis, Ind.

Swann & Co., Birmingham, Ala.

Xylenols:

Barrett Co., New York, N. Y.

Calco Chemical Co., Inc., Bound Brook, N. J.

Reilly Tar & Chemical Corp., Indianapolis, Ind.

Butyl phenol (p-tertiary), Dow Chemical Co., Midland, Mich.

Phenyl phenols, Dow Chemical Co., Midland, Mich.

Resorcinol, tech.:

E. I. du Pont de Nemours & Co., Wilmington, Del.

Pennsylvania Coal Products Co., Petrolia, Pa.

Naphthalene:

Barrett Co., New York, N. Y.

Calco Chemical Co., Inc., Bound Brook, N. J.

Coopers Creek Chemical Co., West Conshohocken, Pa.

E. I. du Pont de Nemours & Co., Wilmington, Del.

Reilly Tar & Chemical Corp., Indianapolis, Ind.

Shell Chemical Co., San Francisco, Calif.

Standard Naphthalene Products Corp., South Kearney, N. J.

White Tar Co. of N. J., Inc., Pittsburgh, Pa.

Phthalic acid and anhydride:

American Cyanamid Co., New York, N. Y.

Barrett Co., New York, N. Y.

E. I. du Pont de Nemours & Co., Wilmington, Del.

Monsanto Chemical Co., St. Louis, Mo.

National Aniline & Chemical Co., Inc., New York, N. Y.

Maleic acid and anhydride:

National Aniline & Chemical Co., Inc., New York, N. Y.

American Cyanamid Co., New York, N. Y.

Monsanto Chemical Co., St. Louis, Mo.

Malic acid, National Aniline & Chemical Co., Inc., New York, N. Y.

Adipic acid, E. I. du Pont de Nemours & Co., Wilmington, Del.

Succinic acid and anhydride:

American Cyanamid Co., New York, N. Y.

National Aniline & Chemical Co., Inc., New York, N. Y.

Urea, E. I. du Pont de Nemours & Co., Wilmington, Del.

Formaldehyde:

E. I. du Pont de Nemours & Co., Wilmington, Del.

Empire Oil & Refining Co., Bartlesville, Okla.

Heyden Chemical Corp., New York, N. Y.

Hexamethylenetetramine, tech.:

E. I. du Pont de Nemours & Co., Wilmington, Del.

Heyden Chemical Corp., New York, N. Y.

Monsanto Chemical Co., St. Louis, Mo.

Furfural, Quaker Oats Co., Chicago, Ill.

Vinyl acetate:

Carbide & Carbon Chemicals Corp., New York, N. Y.

E. I. du Pont de Nemours & Co., Wilmington, Del.

Niacet Chemicals Corp., Niagara Falls, N. Y.

Vinyl chloride, Carbide & Carbon Chemicals Corp., New York, N. Y.

APPENDIX F

GLOSSARY[29]

_Alkyd resin._—Any condensation product involving a polybasic acid and

a polyhydric alcohol. Typical examples are phthalic glyceride and its

modifications containing combined fatty acids or rosin. Representative

examples are Rezyls and Glyptal.

_Aminoplast._—General terms for synthetic resins from amino or amido

compounds. A typical example is urea-formaldehyde.

_Amorphous._—Devoid of crystalline structure. This condition is rare.

Many substances which are apparently amorphous show microcrystallinity,

particularly under X-ray examination.

_A-stage resins._—Thermosetting resins reacted only to the initial stage

where they are soluble and fusible. The normal stage of a resin used for

impregnation.

_Bonding strength._—The amount of adhesion between a binder and filler.

More specifically, the measure of the extent to which the composite

layers of a laminated product are bonded together.

_Brittleness._—Liability to break, generally to a conchoidal fracture.

_B-stage resins._—Thermosetting resins reacted to a stage where they

soften when heated and swell in contact with liquids but do not entirely

fuse or dissolve. This is the preferred stage for the resin in molding

compositions.

_Casting._—Forming a material into a shape by pouring it when liquid into

a mold. The product from the mold is used as such or mechanically worked

in various ways to the final articles, as by sewing, cutting, blanking,

turning, drilling, forming, swaging, grinding, polishing, sanding, or

routing.

_Compressive strength._—Resistance to deformation under applied pressure.

_Condensation._—A chemical reaction in which two or more molecules

combine with a separation of water or some other simple substance.

Applied to synthetic resins it means the formation of a resin by

combination of a number of molecules with elimination of water,

ammonia, hydrogen chloride, or other simple substance. Examples of

condensation resins are alkyd, phenol-aldehyde, and urea-formaldehyde

resins. The final products are also called condensation-polymers. (See

Polymerization.)

_Copolymerization._—The term applied when two or more substances

polymerize at the same time to yield a product which is not a mixture of

separate polymers but a complex having properties different from either

polymer alone. For example, vinylite is produced by polymerization of a

mixture of vinyl acetate and vinyl chloride.

_C-stage resins._—Thermosetting resins in the final stage in which they

are infusible and insoluble. The state of the resin in the final molded

article.

_Curing._—The change of a binder from the soluble-fusible condition

to the substantially insoluble-infusible form by chemical action. The

heat-setting of a resinoid. Action is analogous to vulcanization of

rubber.

_Dielectric strength._—Voltage gradient at which a continuous electrical

discharge will take place between two electrodes when the material in

question is placed between the electrodes and a potential difference is

applied to them.

_Elastic._—A substance which exhibits rubberlike properties or “high

elasticity” over a wide range of applied forces.

_Elastic deformation._—When a substance reverts to its original

dimensions on release of an applied stress.

_Elastic limit._—The point at which a body begins to yield under a

stress; that is, when the stress is equal to or greater than the internal

friction.

_Elasticity._—The property by virtue of which a body reverts to its

normal bulk or shape after deformation by an applied force.

_Extrusion molding._—A molding procedure for extended shapes of uniform

cross section, whereby a heat-softened substance is forced through an

orifice of form coinciding with the cross section of the article.

_Flexibility._—Capability of bending without breaking.

_Gums._—Viscous vegetable secretions which harden but, unlike resins, are

water soluble. The name is often applied, particularly in the varnish

industry, to natural resins such as copals.

_Hardness._—Property of substances determined by their ability to

abrade or indent one another. Often measured by the extent or depth of

indentation produced by a standard substance under a predetermined load.

_Impact strength._—The measure of toughness of a material. Generally

determined by the energy required to break a specimen in one blow.

_Injection molding._—A molding procedure whereby a heat-softened plastic

material is forced from a receptacle into a cavity which gives the

article of desired shape. Used particularly for thermoplastics since

the scrap can be reused. As soon as the composition in the mold cools

sufficiently to be rigid, the mold is opened and the molded article

removed. An analogy of injection molding in another field is shown by the

linotype machine.

_Inserts._—Parts of a finished molded article which are of different

material from the molding composition but are set in place or positioned

by the molding operation.

_Laminated products._—Sheets of material united by a binder. For example,

sheets of paper or wood coated and/or impregnated with a resinous

composition and subjected to pressure, generally with heat.

_Monomer._—The simplest repeating structural unit of a polymer. For

addition polymers this represents the originally unpolymerized compound.

_Phenoplast._—A general term for phenol-aldehyde resins. Synonymous with

popular term “phenolics.”

_Plastics._—All substances that can be molded. In general a plastic is a

substance which behaves as a solid at stresses less than a certain amount

known as the yield value and as a viscous liquid at stresses greater

than this. The name is also applied to substances which originally but

not ultimately fulfill this condition. For example, it is applied to

thermoset compositions or resinoids in the final stages.

_Plasticity._—Susceptibility to and the retention of deformation.

Capacity of taking and retaining the form of a mold. The property of

solids by virtue of which they hold their shape permanently under the

action of small shearing stresses but are readily deformed, worked, or

molded under larger stresses.

_Polymerization._—A chemical change resulting in the formation of

a new compound whose molecular weight is a multiple of that of the

original substances. The products of the reaction are called polymers.

To distinguish from those resulting from condensation (q. v.), they

are often designated addition polymers, since the reaction is that of

successive addition of a large number of relatively small molecules

(monomers) to form the final polymer.

_Power factor._—In an insulating material, the ratio of total power

loss (watts) in the material to the product of voltage and current in a

capacitor in which that material is a dielectric.

_Preforms._—Molding powders converted by pressure and without heat

into a denser coherent form which approximates the shape of the final

hot-pressed article. Molding material converted to preforms has about

half the bulk factor of the original powder. Other forms of densified

composition which do not necessarily approximate the shape of the final

molding are tablets, briquettes, pellets, pills, and balls.

_Resin._—A term generally referring to a physical condition at room

temperature approximating the physical properties of natural resins.

However, the temperature of reference should not be limited to room

temperature and the term is here intended to embrace all substances which

within a certain temperature range show these, properties. For example,

many oil-modified alkyd resins are viscous liquids at room temperature

but not at lower temperatures; polystyrene is a resin at room temperature

but rubberlike when warmed.

_Resinoids._—The class name applied to thermosetting resins. Temporary

thermoplastics. The name is also often applied to the final cured resins.

_Softening point._—Resins have no sharp melting point. Application of

heat causes gradual change from a brittle or exceedingly thick and slow

flowing material to a softer and less viscous liquid. The softening point

is the temperature at which the material flows at a definite rate or to a

definite distance.

_Synthetic resin._—A complex, substantially amorphous, organic semisolid

or solid material (usually a mixture of substances) built up by chemical

reaction of comparatively simple compounds and, depending upon the

temperature at which the examination is made, approximating the natural

resins in various physical properties: namely, luster, fracture,

comparative brittleness, insolubility in water, fusibility or plasticity

when heated or exposed to heat and pressure, and, at a certain more

or less narrow temperature range before fusion, showing a degree of

rubberlike extensibility; but commonly deviating widely from natural

resins in chemical constitution and behavior with reagents.

_Synthetic rubber._—Caoutchouc synthesized in the laboratory. The term is

a misnomer and most probably represents an impossibility.

_Tensile strength._—The greatest internal force per unit of cross section

which a material develops before failure under tension.[30]

_Thermoplastic._—The property of softening under heat. All molding

materials are thermoplastic at the initial application of heat. One class

(the so-called thermoplastics) remains soft permanently under heat; the

other (thermosetting), after first softening, sets or cures more or less

quickly to a more solid form. A practical distinction is that with the

first class the mold must be cooled before the molded article is removed,

but not with the second. A thermoplastic substance is adequately rigid

at normal temperatures and under ordinary conditions of stress but is

capable of deformation under heat and pressure.

_Thermosetting._—The property of undergoing a chemical change when

heated whereby a hardened product is obtained. Property most pronounced

in phenol and urea formaldehyde resins and less so with alkyds. A

thermosetting substance possesses initially the properties of a

thermoplastic but under the influence of heat undergoes chemical change

so that it is no longer thermoplastic but becomes permanently infusible.

_Viscosity._—Internal friction or resistance to change of form of a

liquid. The constant ratio of shearing stress to rate of shear.

_Water-absorption._—Amount of water taken up when exposed to humid

conditions or when immersed. Both rate of absorption and total absorption

are important, also change in dimensions. A certain amount of absorbed

water may improve mechanical properties but usually weakens electrical

characteristics.

FOOTNOTES

[1] A glossary of technical terms is included in appendix F. p. 160 of

this report. There are, however, certain fundamental terms which it would

be advisable to have clearly in mind at this point.

[2] Shellac is a substance secreted by lac insects feeding on certain

types of hardwood trees.

[3] Journal of the Society of Chemical industry, 1901. Vol. 20, p. 1075.

[4] Current sales prices in the United States average between 7 and 10

cents per pound and any imports would be dutiable under the provisions

of par. 28 of the Tariff Act of 1930 at 45 percent ad valorem based on

American selling price plus 7 cents per pound. Based on an American

selling price of 7 cents per pound, the import duty would be slightly

more than 10 cents per pound, while on an American selling price of 10

cents per pound the duty would be 11.5 cents per pound.

[5] Zelov, Victor I. Automatic Molding, Pt. 2, Advantages and

limitations. Modern Plastics, v. 15, No. 2, p. 206; October 1937.

[6] For texts and interpretation of exclusion orders see Treasury

Decisions 41512; 41895; 44411; 44491; 44776; and 44977.

[7] American selling price is defined in section 402, (g) as: “The

American selling price of any article manufactured or produced in the

United States shall be the price, including the cost of all containers

and coverings of whatever nature and all other costs, charges, and

expenses incident to placing the merchandise in condition packed ready

for delivery, at which such article is freely offered for sale to all

purchasers in the principal market of the United States, in the ordinary

course of trade and in the usual wholesale quantities in such market, or

the price that the manufacturer, producer, or owner would have received

or was willing to receive for such merchandise when sold in the ordinary

course of trade and in the usual wholesale quantities, at the time of

exportation of the imported article.”

[8] United States value is defined in section 402, (e) as: “The United

States value of imported merchandise shall be the price at which such

or similar imported merchandise is freely offered for sale, packed

ready for delivery, in the principal market of the United States to all

purchasers, at the time of exportation of the imported merchandise, in

the usual wholesale quantities and in the ordinary course of trade, with

allowance made for duty, cost of transportation and insurance, and other

necessary expenses from the place of shipment to the place of delivery, a

commission not exceeding 6 per centum, if any has been paid or contracted

to be paid on goods secured otherwise than by purchase, or profits not to

exceed 8 per centum and a reasonable allowance for general expenses, not

to exceed 8 per centum on purchased goods.”

[9] The reclassifications read:

PAR. 2. “Vinyl acetate, polymerized or unpolymerized, and synthetic

resins made in chief value therefrom, not specially provided for.”

PAR. 11. “Synthetic resins made in chief value from vinyl acetate, not

specially provided for.”

[10] See sections on import under each resin.

[11] Reduced May 23, 1934, from 25 cents per pound and 30 percent by

Presidential proclamation under Section 336 of the Tariff Act of 1930.

[12] Based on the total sales in 1937 reported to the Tariff Commission;

sales in dollars dived by quantity (net resin content).

[13] The new consumption-restriction regulations are—

_Exterior use on plaster, brick, stone, and cement_:

1. Surfaces already painted with oil paint may be repainted with

oil paints, without restrictions;

2. Surfaces calcimined may be painted with paints containing not

more than 15 percent oil;

3. Unpainted surfaces may be painted only with paints free of oil.

_Exterior use on wood_:

Linseed oil paint may be used for the first coat, and succeeding

coats may contain up to 70 percent oil.

_Exterior and interior use on metal_:

Oil paints may be used without restriction.

_Interior use on plaster, brick, stone, and cement_:

1. Surfaces already painted with oil paint may only be repainted

with paint containing not more than 15 percent oil.

2. Unpainted surfaces must be painted with paint free of oil.

_Interior use on wood, to be cleaned with soap and soda_:

El Varnish and oil varnish may be used for the first coat

followed by paint containing up to 70 percent oil.

_Interior use on wood, not cleaned with soap and soda_:

As above, except that succeeding coats may contain not more than

40 percent oil.

[14] Acknowledgment: Most of the information about the industry in Great

Britain was submitted by Norman Inwood of the staff of the American

consulate general at London, England.

[15] Acknowledgment: Information obtained on the synthetic resin industry

in France was furnished by Addison E. Southard, American consul general

at Paris.

[16] Acknowledgment: Much of the information on the Japanese synthetic

resin industry included herein was furnished by Carl H. Boehringer,

Assistant Trade Commissioner at Tokyo at the request of the U.S. Tariff

Commission.

[17] These figures are based on an average naphthalene content of coal

tar of slightly less than 10 percent. The total amount contained would,

of course, not be recovered even under ideal market conditions as to

price and demand.

[18] Par. 1651. Coal-tar products: ... naphthalene which after the

removal of all the water present has a solidifying point less than 79° C.

... (Free).

[19] Par. 27. Coal-tar products:

(_a_) (1), (5) ... naphthalene which after the removal of all water

present has a solidifying point of 79° C. or above; all the foregoing

products in this paragraph whether obtained, derived, or manufactured

from coal tar or other sources; ... 40 percent ad valorem and 7 cents per

pound.

Synthetic resins and their raw materials A survey of the types and uses of synthetic resins, the organization of the industry, and the trade in resins and raw materials, with particular references to factors essential to tariff consideration. Under the general provisions of section 332, title III, part II, Tariff act of 1930. · 第 21 / 22 段