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Publication numberUS2523461 A
Publication typeGrant
Publication dateSep 26, 1950
Filing dateMar 15, 1946
Priority dateMar 15, 1946
Publication numberUS 2523461 A, US 2523461A, US-A-2523461, US2523461 A, US2523461A
InventorsAngelillo Olindo R, Young John T
Original AssigneeAngelillo Olindo R, Young John T
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Plating with metal carbonyl
US 2523461 A
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Description  (OCR text may contain errors)

Patented Sept. 26, 1950 UNITED STATES PATENT OFFICE J ohnT. Young-and Olind'oiR. Angelillo, :Los .Angeles, Calif.

NoTDrawing Application March 15, 1946, "Serial N0.'7654,'81'8 2-Olaims. 1

This invention relates to methods for plating or coating various surfaces with metalsand more particularly relates to coating metal surfaces. One of the important Objects of the invention is to provide a non-porous, continuous coating of metal capable of sealing the capillary channels along the boundaries of the metal grains which make up the surface of the metal body being plated. This object has been attained with carbonyl solutions.

The ultimate object accomplished by such coating of metals is the complete avoidance of corrosion of the coated metals.- The thorough sealin of the pores of a readily corrodible metal by a continuous coating of a suitable metal such as nickel, chromium, and the like, apparently prevents aspiration, or breathing of the base metal, thereby preventing corrosion. Also, the formation of fungus growths on metal surfaces, has also been prevented in accomplishing the objects of the present invention.

A further object of the invention is to provide a process for applying continuous metal coatings of such tenuity that they may be used for plating precision instruments and the like without afiecting the dimensional tolerances permitted, such coatings -atthe same time being uniform and providing complete protection against corrosion.

A further object is to provide a process for the coating of metals and other objects with thin metal layers which will not check 'or crack in subsequent use and which at the same time will be so tenaciously bonded to the surface of the articles that such coatings cannot be caused to separate.

Accordin to the principal embodiment of this invention, metal surfaces, such as iron, brass and the like, are provided with very thin protective nickel coatings by employing appropriate solutions of nickel carbonyl.

Suitable solvents are hydrocarbons which are normally volatile, and therefore not capable of interfering with the plating operation. For example, benzol, toluol, hexane, octane, sulphurfree gasoline and kerosene, and kindred aromatic and aliphatic hydrocarbons may be employed. However, hydrocarbons of oily nature which are relatively non-volatile will so coat the surfaces of the articles being plated as to prevent deposition of metal upon such surfaces and may not be used. In other words solvents may not be employed having boiling points above about 450 F. Also hydrocarbons contaminated with oxygen, sulphur, chlorine and other halogens, and

the like, are not acceptable because they usually result-in the formation of black deposits instead 'of the desired pure metal deposits. In other words, :so far as isnow known, only substantially pure hydrocarbons within the indicated ranges of volatility :are acceptable.

The carbonylto be employed according to this invention is preferably nickel :carbonyl .NiQCOM.

"tent must be avoided because the carbonyl is extreme'ly unstable in the presence of water.

The coating or plating operation is accomplished by emp loying an indicated solution of nickel carbonyl, as distinguished from nickel carbonyl in gaseous or vapor form, the temperature of the liquid being held at or below about 80 F. for best results. For example, the solution temperature may be about 100 F. or as low as 20 F. The article to be coated is heated preferably to a temperature of around 500 F2, or between about 500 F. and 575 F., and is then quickly dipped into the carbonyl solution, the

time of contact being so short that the temperatureof the object being coated will not fall below about 450 F. or in any event not below 400 F. I Otherwise, instead of obtaining a lbright nickel metal surface, black stains or streaks are formed, thereby resulting in an improper coating not providing a continuous uniform metal seal. Thus, the article must be heated at least to 450 F. The practical upper temperature limit to which the article may be raised is about 575 F. The apparent absolute upper limit is 625 F., beyond which decomposition appears to be of such nature that proper coating cannot be obtained. The time interval for dipping will vary according to the temperature to which the article is heated and to its size. For example, the time may be from a half second for an object weighing 15 grams to 5 seconds for an object weighing 1000 grams, and correspondingly greater times for heavier articles.

The coating phenomenon involves decomposition of the carbonyl, that is the carbonyl radical separates from the nickel so that the nickel deposits upon the article being coated. The coating action is not a. straight line action like that of electroplating, but the nickel moves in all directions and deposits uniformly on all faces. As a consequence, this method of coating is highly satisfactory for plating threaded and other irregular surfaces where a coating of absolutely uniform thickness is required.

It is to be noted that temperature within the limits stated is a critical factor, and that time is also an important factor in so far as it concerns maintenance of temperatures within the indicated limits. However, as the stated limits indicate, there is a considerable choice of temperatures to which articles to be coated may be heated. Heating of the articles to be coated may be accomplished in any manner appropriate for the particular operation. Such may be oven heating, induction heating by electric coils, or otherwise as desired.

It is, of course, necessary to provide above the plating solution an atmosphere which is inert under the operating conditions and from which all oxygen and water vapor are excluded, as well as sulphur, chlorine, and other reactants. Appropriate inert atmospheres are those represented by nitrogen, helium and carbon dioxide. Carbon dioxide is preferred because it is heavier than air and easy to supply. Carbon monoxide liberated by the decomposition of the carbonyl passes into the inert gaseous blanket which in practice is confined, the carbon monoxide being recovered therefrom for the preparation of additional nickel carbonyl.

When an article has been dipped and withdrawn from the solution, it should be retained in the inert atmosphere above the bath until the surface temperature has dropped below about 300 F. whereby to avoid oxidation of the freshly deposited metal. For this cooling function, the equivalent of the inert atmosphere may be used, such as pure benzol, kerosene or even water, or a solution containing a deoxidizing agent, such as sodium sulfite, pyrogallic acid, or the like, the

article being plunged into such liquid until the required cooling is efiected. However, an inert atmosphere must be maintained above the cooling liquid such as that maintained above the plating solution. Although water vapor must be excluded from the inert atmosphere above the solutions, in order to prevent the nickel from turning black, water may nevertheless be .employed as a cooling agent since it does not appear to affect the metal coating due to the very quick cooling of the article when plunged into water. However, in using water, it is preferable that it contain a deoxidizing agent as above indicated.

The individual coatings produced by the method of this invention are continuous and'of uniform thickness in the order of a few millionths of an inch, or perhaps between about 0.00001 and .000001 inch. Such a coating may represent for example the application of 0.03

milligram per square inch of coated surface. It

is thus apparent that the present process provides coatings so thin that they do not interfere with the tolerances required in the production of precision instruments. It is further apparent that the characteristic of the process by which the metal coating is uniformly applied regardless of surface irregularities, as contrasted with uneven applications on irregular surfaces by electroplating, isof much importance. Whe1 je increased thickness is required, dippings may be repeated, each successive layer being applied in uniform thickness so that the ultimate coating is uniformly thick. These coatings, individually comparable in some respects with molecular layers, thus permit the building of multiple layers to any desired degree in order to insure protection against corrosion without in any way producing undue thickness or overstepping permissible tolerances.

Employment of preferred nickel carbonyl according to the process of this invention for the deposition of nickel coatings of extreme thinness is of great importance, especially from the standpoint of corrosion, inasmuch as pure nickel coatings are of very low porosity. In this respect nickel is superior even to chromium and apparently to all other metals and therefore best for this particular purpose. The value of the metal whose carbonyl is employed lies fundamentally in its own porosity. The less porous and more continuous the metal coating, the greater its value in preventing corrosion. Nickel which has been deposited from nickel carbonyl r is considerably more resistant to corrosion than nickel deposited by any other means, this being due probably to higher purity.

For some purposes it may also be possible to employ solutions of other metal carbonyls in appropriate solvents, such as the indicated hydrocarbon solvents. These carbonyls might be represented by chromium and tungsten carbonyls, and possibly by molybdenum carbonyl, all of these normally being solids and soluble in appropriate organic solvents. As previously indicated, solutions of only very low concentrations need be employed e. g. from about 1% to as low as 0.001% of the metal carbonyl, however, higher concentrations may be used if desired, for example l Inasmuch as the activity of the metal increases asconcentration decreases, coating efficiency is maintained even after the concentration has been lowered to relatively insignificant percentages by repeated dippings.

A further advantageous feature which we have discovered is that with a carbonyl such as nickel carbonyl, very low temperatures of the carbonyl solutions are desirable especially where thick coatings are desired. Thus, a solution of nickel carbonyl in toluene may be used at 0 F. or as low as 20 F. The result is a much thicker plating than when operating at F., for example around five times as thick, and at the same time greater solution stability is obtained. Such temperatures are quite feasible with nickel carbonyl whose freezing point is 25 F., and coating thicknesses perhaps in the order of 0.00002 inch are obtained. With other carbonyls low temperatures may be employed approaching those at which. the carbonyl freezes out of solution.

Since variations in the generic process herein disclosed will become apparent to those skilled in the art to which this improvement relates, it is intended to'cover all such modifications as fall within the scope of the claims.

We claim as our invention:

1. A coating process comprising: heating an object to a temperature between about 450 F. and 600 F.; dipping the heated object into a solution of a metal carbonyl in a hydrocarbon to deposit a metal coating, the temperature of the carbonyl solution approaching the freezingout point of the carbonyl; removing the object before its surface temperature drops below about 5 400 F.; reheating the object; re-dipping the object to deposit an additional coating of metal; removing the object as before; and cooling.

2. A process as in claim 1 wherein the carbonyl is nickel carbonyl and the temperature of the solution is in the order of 0 F. to 20 F.


REFERENCES CITED The following references are of record in the file of this patent:

Number 10 Number Great Britain Dec. 9, 1936

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Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2698810 *Aug 25, 1950Jan 4, 1955Nat Res CorpCoating process
US2742691 *Apr 18, 1950Apr 24, 1956Ohio Commw Eng CoMethod of making corrosion resistant clad steel
US2753800 *Mar 24, 1952Jul 10, 1956Ohio Commw Eng CoProduction of printing plates
US2760261 *Apr 17, 1952Aug 28, 1956Ohio Commw Eng CoMethod of bonding articles
US2829170 *Jul 26, 1954Apr 1, 1958Texas CoProcess for decobalting a liquid carbonylate
US2881094 *Jul 16, 1953Apr 7, 1959Hoover Thomas BProcess of coating with nickel by the decomposition of nickel carbonyl
US2886468 *Jul 16, 1953May 12, 1959Thomas B HooverNickel plating process
US2918392 *Jan 4, 1957Dec 22, 1959Gen Aniline & Film CorpMethod of depositing metal in the pores of a porous body
US3041197 *Jun 1, 1959Jun 26, 1962Berger CarlCoating surfaces with aluminum
US3075858 *Jan 21, 1958Jan 29, 1963Union Carbide CorpDeposition of composite coatings by vapor phase plating method
US3155532 *Nov 10, 1960Nov 3, 1964Union Carbide CorpMetal plating process
US3214288 *Dec 14, 1961Oct 26, 1965Nat Steel CorpProcess for the deposition of metallic aluminum
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US3449150 *Mar 31, 1965Jun 10, 1969Continental Oil CoCoating surfaces with aluminum
US3464844 *Mar 2, 1967Sep 2, 1969Continental Oil CoAluminum plating of surfaces
US3508977 *Jan 11, 1967Apr 28, 1970Union Carbide CorpProcess for producing metal borides on the surface of metals
US3549412 *Apr 29, 1968Dec 22, 1970Ethyl CorpMetal plating particulated substrates
US3652322 *Sep 3, 1970Mar 28, 1972Continental Oil CoMethod for controlling the heating of a metal immersed in a plating solution
US4373162 *Oct 28, 1981Feb 8, 1983Control Data CorporationLow frequency electronically steerable cylindrical slot array radar antenna
US4457957 *Aug 26, 1980Jul 3, 1984American Glass Research, Inc.Fatty acid ester or silicone oil vehicle
U.S. Classification427/314, 427/229, 427/319
International ClassificationC23C16/00, H01C17/20
Cooperative ClassificationC23C16/00, H01C17/20
European ClassificationH01C17/20, C23C16/00