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Publication numberUS2685535 A
Publication typeGrant
Publication dateAug 3, 1954
Filing dateFeb 1, 1951
Priority dateFeb 1, 1951
Publication numberUS 2685535 A, US 2685535A, US-A-2685535, US2685535 A, US2685535A
InventorsHerman Nack
Original AssigneeOhio Commw Eng Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method and apparatus for deposition of materials by thermal decomposition
US 2685535 A
Abstract  available in
Images(1)
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Claims  available in
Description  (OCR text may contain errors)

Aug. 3, 1954 H. NACK 2,635,535

METHOD AND APPARATUS FOR DEPOSITION OF MATERIALS BY THERMAL DECOMPOSITION Filed Feb. 1', 1951 INVENTOR HERMAN NACK Wm ,1 mm

ATTORNEYS Patented Aug. 3, 1954 METHOD AND APPARAT OF MATERIALS BY T 'SITION US FOR DEPOSITION HERMAL DECOMPO- Hermjan Naek, Troy, Ohio, assignor to The Gommonweaxlth- Engineering Company of Ohio, Dayton, Ohio, a corporation of Ohio Application February 1, 1951, Serial No. 208,934

4 Claims.

This .invention relates to the art of deposition of metals. More particularly, it relates to the plating of metals from the gaseous. state, and to the apparatus for carrying out the saidprocess.

The deposition of thinfilms of protective metal, .such as nickel, cobalt, tungsten and molybdenum, or their alloys, on metallic bases has been accomplished by enclosing an object to be plated in a chamber, filling the chamber with decomposable metal-bearing gas, heating the object to be plated to the decomposition temperature of the said gas, and allowing the metal-bearingg-as-to contact the heated plate and be deposited thereon.

Considerable :diificulty has been experienced in securing dense film deposits withsuch a method 1 and various expedients have been devised'to overcome the inherent limitations of the structure of thisapparatus. These limitations stem from two primary causes. The first of these is that the gaseous decomposition may take place prematurely, that is, before the gas contacts the article .to be plated, thus permitting metal particles to fall upon the surface to be plated resulting in roughness of the plate coating.

Secondly, an interracial resistance between the advancing wave of plating .gas and the surface of the object to be plated opposes the decomposition directly on the 'free surface of the object.

The result of these effects of uncontrolled decomposition is the production of thin, porous, irregular coatings of deposited metal. While, as

noted above, means to effect the control of these undesirable phenomena have been accomplished they require expert workmanship and specialized apparatus.

It is an object of this invention to provide a method by which the above mentioned disadvantages are overcome.

It is an important object of this invention to provide a novel method for gas plating by which a firmly adhering metal coating is obtained.

It is a principal object of this invention to provide a method of gas plating which yields coatings of increased density.

It is also an object of this invention to provide a metal coating which will withstand elevated chamber i More specifically, in the process of invention the application of an electrostatic field which has the workpiece as one electrode thereof causes ionized gases to be directed to the workpiece at great velocity. While in heated gases the collisions between molecules give rise to ionization to some degree, it is desirable to increase this velocity of collision by means or the electrostatic field and the presence of charged gases in the plating chamber by exposing the gases, both carrier and platin gas, to radioactive substances prior to their entry to the chamber.

It should also be noted that it is preferable to secure the second electrode of the electrostatic field to a conductive outlet portion of the chamber whereby the negatively charged gases of decomposition will be attracted thereto and rapidly swept from the chamber. This mode of operation results in decreasing the resistance to the flow of metal-bearing vapors to the surface of the metal to be plated and thus provides for intimate contact of the metal-bearing component with the surface and gives rise to dense uniform non-porous deposits.

The nature and purpose of this invention has been indicated in a general way and there follows a more detailed description of the preferred embodiments of the invention with reference to the accompanying drawing in which:

Figure 1 is a view partly in section of the apparatus of invention; and

Figure 2 is a View of apparatus utilized in carrying out one embodiment of the invention.

Referring to Figure 1, there is shown a charm her I having a gas inlet 2 and an outlet 3 electrically insulated from the chamber. Mounted in the chamber is a heating unit 4 connected to a source of energy (not shown) by an insulated lead it extending through the wall 5 of the Supported on the heating unit 4 by electrically insulating support members it is a workpiece S to which there is electrically secured an electrically conductive lead i passing through the wall 5 in electrically insulated relation therewith.

The connection between the workpiece 6 and the lead i may be through means of any suitable contact arrangement, such as clamps, sockets, or the like. Electrically connected to the vopposing end of the lead '3- is the negative pole of a source of direct current, generally indicated at 8. The positive pole of the source 8 is connected by a lead '9 to a conductive portion of outlet 3, thereby setting up an electrostatic field between the inner end, of the outlet 3. and-the workpiece B. The outer end of the outlet 3 is preferably of insulating material but in some instances may be conductive and in such a case is insulated from ground.

In operation metal-bearing gases together with a carrier gas are fed to the chamber i through the inlet 2 from suitable containers or mixing chambers which are not shown since they are well known to the art and form no part of the present invention.

The entering gases due to their velocities and frequent collisions may be ionized to a very slight extent and are attracted to the workpiece or cathode 6. The negatively charged cathode will receive the positively charged molecules, causing decomposition of the metal-bearing gases into metallic ions and negatively charged ions of the gases of decomposition. The metallic ions lose their charge to the cathode, resulting in a metal deposit, while negatively charged decomposition products will be repelled with great force and at high velocity from the area of the plated surface.

These repelled ions move under the influence of the electrostatic field to the positively charged outlet of the chamber, and in so doing strike or collite with un-ionized gases thereby contributing to the overall ionization of the gas in the chamber. Accordin ly when in full operation the chamber will contain large quantities of positively charged metallic ions, and negatively charged gases of decomposition which may in the ionized state or as charged molecules of carbon monoxide, carbon dioxide, and so forth. The charged metallic ions moving at high velocity towards the cathodic workpiece will deposit thereon in a fine, uniform dense coating, thus overcoming the defect noted hereinbeiore of par ticles settling slowly and forming a rough surface.

It is clear from the foregoing that while it is preferable to have the electrostatic field applied between the workpiece and the outlet of the chamber that the only requirement for impinging the metallic positively charger. ions on the.

workpiece is that the workpiece be the cathode. The positive plate or" the electrostatic field may be any other suitable conductive portion of the apparatus.

The electrostatic voltage necessary to effect the novel plating process set forth will be a able factor dependent upon the distance between the plates of the field, the nature of plating gas, the pressure and temperature of this gas, and so forth. Other conditions being equal field strength will decrease as the distance from an electrode increases, and an electrostatic potential of 1000 volts applied to the plates will be decidedly effective at a distance of between plates. Where the anode and cathodic workpiece are separated by as much as 2 feet approximately 200,909 volts may be required for maximum effectiveness. However, as been noted, the gas pressure and the nature of the gas may require alteration in these conditions.

The heater unit t is utilized to raise the ternperature of the cathode workpiece to accomplish complete decomposition of the metal hearing' gas at the workpiece surface. This temperature is a variable factor dependent upon the plating gas used, and in the case of nickel carbonyl gas'should be in excess of 180 C.

Base materials which may be plated in the foregoing manner are steel, copper, aluminum, cast iron, brass, magnesium, and the like.

The process and apparatus of invention are applicable for plating with all metals which form gaseous carbonyls, such as chromium, iron, tungsten, cobalt, molybdenum, tellurium, rhenium and nickel. The carbonyl of each of these metals has a temperature at which decomposition is complete, although some decomposition takes place at lower temperatures. The adverse eiiects of such low temperature decomposition are overcome by the high velocity attained by the particles in the electrostatic field.

In the case of tungsten, nickel, chromium and iron carbonyls it is preferred to maintain the temperature of the workpiece in the range of 350 F. to 425 F., although temperatures below and above this range may be utilized and good plating accomplished. The use of the electrostatic field with the. attendant high velocity of the particles permits a reduction in the temperature of the workpiece if other conditions require it.

In Figure 2 there is shown a tubular member ill having an inlet H and outlet l2 and containing radioactive material, such as uranium or radium, The function of the member ill is to effect a preliminary ionization of either the car rier gas which enters the plating chamber with the metal carbonyl, or to efiect preliminary ioniaction of both the carrier gas and the carbonyl. For this latter purpose outlet 52 of member It! may be connected directly to inlet 2 of chamber l.

The eiiect of the action of the radioactive material is to cause a splitting of the carbonyl molecule M (CO-i) into positively charged M ions and negatively charged (CO4) ions. Since the metallic ions are now dissociated from the heavier (CO4) ions the velocity imparted to them by the electrostatic field, before striking the workpiece, will be considerably greater than had. dissociation taken place closer to the object to be plated.

The charged carrier gas serves to effectively attract the gases of decomposition from the area of the plating surface, thus further tending to break down the interfacial resistance between the wave of plating gas and the surface of the cathodic workpiece.

Carrier gases useful for the above purpose are nitrogen, helium, hydrogen, carbon dioxide and other inert media. Hydrogen it may be noted is particularly useful since it effects a reducing action and may accordingly be advantageously used under conditions where iron rust might develop and inhibit the process.

While the above embodiments of the invention have particularly set forth the use of carbonyls, it will be understood that other metal bearing gaseous compounds such as metal hydrides, metal alkyls, metal halides and the nitroxyls such as that of copper, the nitroxyl carbonyls and the carbonyl halogens fall within the scope of this invention and may be used with equal facility.

Cleaning of the workpiece preparatory to coating may be effected by any of the means well known to the art, such as acid, alkali, or electrochemical treatment, the only requirement being that a clean metal surface be provided for the reception of the deposited metal to attain the maximum benefit from the novel method of deposition.

It will be understood that this invention is susceptible to modification in order to adopt it to different usages and conditions and, accordingly, it is desired to comprehend such modifications within this invention as may fall within the scope of the appended claims.

I claim:

1. An apparatus for coating an electrically conductive workpiece comprising a chamber having an inlet and an outlet, a support for said workpiece in said chamber, means for creating a high voltage electrical field Within said chamber and having anode and cathode terminals disposed therein, said cathode being arranged for connection to said workpiece on said support, said anode being arranged at said outlet, and means comprising a tubular member having an inlet and outlet and containing radioactive material, said outlet of the tubular member being connected to the inlet of said chamber, means for heating said workpiece and means to supply a stream of gaseous metal carbonyl to the inlet of said tubular member.

2. An apparatus as called for in claim 1 wherein the radioactive material is selected from the group consisting of radium and uranium.

3. A method of coating an electrically conductive workpiece comprising the steps of supporting the workpiece within a chamber, creating an elec- References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 1,820,878 Wyckolf Aug. 25, 1931 1,866,729 Spanner July 12, 1932 2,332,309 Drummond Oct. 19, 1943 2,510,795 Blau et al June 6, 1950 FOREIGN PATENTS Number Country Date Great Britain of 1947

Patent Citations
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US1820878 *Sep 22, 1926Aug 25, 1931Doherty Res CoCatalytic combustion by means of refractories
US1866729 *Apr 30, 1929Jul 12, 1932Electrons IncMethod of obtaining metallic coatings
US2332309 *May 20, 1940Oct 19, 1943Ohio Commw Eng CoGaseous metal deposition
US2510795 *Dec 29, 1945Jun 6, 1950Canadian Radium & Uranium CorpAlpha ray source and method of producing same
GB589966A * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2876137 *Apr 12, 1955Mar 3, 1959Ohio Commw Eng CoMethod of plating metal with magnesium
US2881514 *Apr 12, 1955Apr 14, 1959Ohio Commw Eng CoAluminized magnesium products and method of making
US2887406 *Dec 14, 1956May 19, 1959Ohio Commw Eng CoGas plating of titanium
US2887984 *Jun 24, 1954May 26, 1959Ohio Commw Eng CoApparatus for gas plating continuous length of metal strip
US2907626 *Jan 15, 1958Oct 6, 1959Bjorksten Res Lab IncMetal coating of glass fibers at high speeds
US2999216 *Feb 23, 1960Sep 5, 1961Tung Sol Electric IncBallast tube
US3228373 *Mar 26, 1964Jan 11, 1966Drexel Inst Of TechnologyFurnace for producing oriented graphite
US3239368 *Apr 26, 1962Mar 8, 1966Nra IncMethod of preparing thin films on substrates by an electrical discharge
US3326178 *Sep 12, 1963Jun 20, 1967Angelis Henry M DeVapor deposition means to produce a radioactive source
US3366090 *Apr 7, 1966Jan 30, 1968Air Force UsaGlow discharge vapor deposition apparatus
US3371649 *Sep 9, 1966Mar 5, 1968Technical Ind IncMeans for controlled deposition and growth of polycrystalline films in a vacuum
US3756193 *May 1, 1972Sep 4, 1973Battelle Memorial InstituteCoating apparatus
US5011708 *Jun 6, 1989Apr 30, 1991University Of Virginia Alumni Patents FoundationUse of radioactive nickel-63 to inhibit microbially induced corrosion
US5391252 *Jun 2, 1994Feb 21, 1995Hughes Aircraft CompanyPlasma pressure control assembly
Classifications
U.S. Classification427/458, 427/5, 118/64, 118/723.00E, 427/58
International ClassificationC23C16/448, C23C16/48
Cooperative ClassificationC23C16/48, C23C16/448
European ClassificationC23C16/48, C23C16/448