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Publication numberUS3046159 A
Publication typeGrant
Publication dateJul 24, 1962
Filing dateDec 17, 1957
Priority dateDec 17, 1957
Publication numberUS 3046159 A, US 3046159A, US-A-3046159, US3046159 A, US3046159A
InventorsBrookshire Robert R
Original AssigneeHughes Aircraft Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method of copper plating by chemical reduction
US 3046159 A
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Description  (OCR text may contain errors)

3,046,159 METHOD OF COPPER PLATING BY CHEMICAL REDUCTION Robert R. Brookshire, Canoga Park, Calif., assignor to Hughes Aircraft Company, Culver City, Calif., a corporation of Delaware No Drawing. Filed Dec. 17, 1957, Ser. No. 703,292 3 Claims. (Cl. 117-130) This invention relates to electroless plating by the deposition of metals by chemical reduction. More particularly the invention relates to improvement in the deposition of copper from chemical reduction plating solutions.

The chemical reduction process for plating has several advantages over conventional metal electroplating methods. Chemical reduction plating provides a deposit of substantially uniform thickness over articles having complex shapes and other irergularities such as small recesses and apertures. Even the remote surfaces in such recesses may be uniformly plated by the chemical reduction process in contrast with conventional electroplating methods :where the plating of such recesses is a practical impossibility. Known prior chemical reduction processes, however, all employ soluble metallic compounds which are exceptionally light-sensitive and therefore easily reduced. It will be appreciated that the ease of reduction of such light-sensitive compounds renders the process difficult to control. Generally in order to achieve control it is necessary to carry out the processes under darkroom conditions or to include other additives in the plating solution which increase the solubility of the compounds and thus reduce the light sensitivity thereof. Attempts to increase the solubility of metallic compounds in aqueous solutions have not been markedly successful and such solutions have, in general, failed to produce a good plate.

It is therefore an object of the instant invention to provide an improved method for plating suitable surfaces with copper by a controllable chemical reduction process.

According to the invention a chemical reduction plating solution is employed in which an insoluble compound of copper is included. Since an insoluble copper compound is employed, the plating reaction is not adversely affected by light and greater control of the plating process is thus obtained. The insoluble compound is reduced by including in the plating solution a soluble compound which forms a soluble complex with the insoluble compound. This complex is then reducible upon -a suitable surface by the action of a reducing agent.

Examples of metals and alloys which may be coated or plated with copper by the practice of the present invention include steel, iron, ferrous alloys, nickel, cobalt, gold, silver, platinum, copper, copper base alloys, magnesium, and aluminum. It will be understood that superior copper plating results when the surface of the article to be coated is thoroughly cleaned. Hence, in most instances it is desirable to employ conventional plating pretreatments, such as buffing, abrading, or acid etching prior to chemical reduction plating.

In the practice of a specific embodiment of the invention an improved copper deposit or plating is obtained by immersing an article having a surface to be plated into an aqueous solution in contact with water-insoluble cupric oxide and containing, a reducing agent such as sodium hypophosphite, and a chelating or complex-ing agent such as ammonium sulfate or ammonium chloride. The purpose of the complexing agent is to maintain a relatively small portion of the copper in solution in a watersoluble copper complex while permitting a relatively large portion of the copper in the water-insoluble copper oxide to remain out of solution as a copper reserve in contact with the aqueous plating solution. The reduction plating is continued until a predetermined thickness of platnited States Patent l 3,046,159 Patented July 24, 1962 ing is obtained or until the copper ion content in the solution and the reserve supply of copper oxide are substantially exhausted. The function of the chelating or complexing agent is to continuously form a soluble complex with the insoluble copper compound and to continuously hold the copper in solution in a controlled concentration until reduced to the metallic state. During the plating process the plating solution bath is maintained at a temperature in the range of from about 50 C. to about C. At the higher temperature the plating rate is increased and becomes more difficult to control. Chelating or complexing agents suitable in the chemical reduction plating processes of the instant invention are ammonium sulfate and ammonium chloride. The reducing agent is preferably the hypophosphite radical which may be introduced as an alkali metal hypophosphite such as sodium or calcium hypophosphite, ammonium hypophosphite, or as hypophosphorous acid.

A chemical reduction plating solution in accordance with the present invention is formed by adding the insoluble copper compound and the soluble chelating or complexing agent to water. The amount of insoluble copper compound is determined by the amount necessary to deposit a desired thickness of copper on a particular surface which amount can, of course, be calculated for a particular article. The ratio of the chelating or complexing agent to the insoluble copper compound is not critical. However, it will be understood that if an ion ratio of greater than about 5 to 1 chelating agent to insoluble compound is employed, the copper ion is held so strongly in solution by the chelating agent that its reduction therefrom becomes diflicult and the plating process becomes less controllable. Likewise employing a ratio of less than about 0.025 to 1 chelating agent to insoluble compound results in an extremely low rate of plating or no plating at all since there is an insufficient amount of chelating agent to form a significant amount of soluble complex. The hypophosphite reducing agent is then added to the solution, the quantity being determined by the amount of copper to be reduced. In general it is advisable to provide an excess amount of hypophosphite radical to accommodate side reactions and to maintain the plating reaction during the final reduction stages. It has been found that excellent results are obtainable when an ion ratio of hypophosphite radical to insoluble copper compound of 05-40 to 1 is employed.

The following are illustrative examples of initial plating bath compositions and conditions in accordance with the present invention wherein the quantities, where applicable, are expressed in terms of grams per litre:

NaH PO .H O NH Cl 0.1 Temperature, C. 93.0 P 3.0 Work load (cmF/cmfi) 0.25 Average plating rate (mgs./cm. /hr.) 160-175 Example 4 CuO 3.0 NaH2PO2.H2O 1 NH Cl 0.1 Temperature, C. 93.0 pH 3.0 Work load (cm. /cm. 0.25 Average plating rate (mgs/cmP/hr.) 30.0

The acidity of the solutions in the above examples was adjusted by the addition of a few drops of concentrated H 50 so that the solutions had a pH value of about 3.0.

It will thus be understood from the foregoing description and examples of the invention that an improved method of plating copper by chemical reduction has been provided in which the reduction action is not sensitive to light and is more controllable whereby an improved plating of copper is obtained. It should be understood that, although the invention has been described with specific reference to particular embodiments thereof, it is not to be so limited since changes and alterations therein may be made which are within the intended scope of the invention as defined in the claims appended.

What is claimed is:

1. The method of copper plating comprising the step of contacting the surface to be plated with an acidic plating solution at a temperature in the range of from about to about C., consisting essentially of a dissolved ammonium salt, a dissolved hypophosphite reducing agent, dissolved copper ions, and an undissolvedcopper ioncontaining compound in contact with the plating solution, the ion ratio of said hypophosphite ion to the undissolved copper ion being in the range of from about 0.5 to about 40, and the ion ratio of the ammonium ion of the dissolved ammonium salt to the undissolved copper ion being in the range of from about 0.025 to about 5.

2. The method according to claim 1, wherein the undissolved copper compound is copper oxide.

3. The method according to claim 2, wherein the plating solution is maintained at a pH of about 3.

References Cited in the file of this patent UNITED STATES PATENTS 2,472,393 Avallone et al June 7, 1949 2,519,672 Lawless Aug. 22, 1950 2,702,253 Bergstrom Feb. 15, 1955 2,703,295 Kantrowitz Mar. 1, 1955 2,726,969 Spaulding Dec. 13, 1955 2,791,516 Chambers et al May 7, 1957 2,852,450 Mundell Sept. 16, 1958 2,872,346 Miller Feb. 3, 1959 2,872,359 Sau-bestre Feb. 3, 1959 2,874,072 Cahill et a1. Feb. 17, 1959

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2472393 *Sep 25, 1944Jun 7, 1949American Steel & Wire CoProcess and bath for copper coating ferrous metal
US2519672 *Jan 13, 1947Aug 22, 1950Lawless Charles FComposition for bluing metal
US2702253 *Nov 1, 1950Feb 15, 1955Gasaccumulator Svenska AbSurface metallizing method
US2703295 *Oct 7, 1952Mar 1, 1955Kantrowitz Morris SNonelectrolytic method for making bimetallic offset printing copper plating composition and method of plating
US2726969 *Dec 3, 1953Dec 13, 1955Gen Motors CorpChemical reduction plating process
US2791516 *Sep 17, 1953May 7, 1957Gen Motors CorpElectroless plating
US2852450 *Jun 10, 1954Sep 16, 1958Donnelley & Sons CoMethod of copper plating
US2872346 *May 21, 1956Feb 3, 1959Adolph MillerMetal plating bath
US2872359 *Dec 3, 1956Feb 3, 1959Sylvania Electric ProdCopper sensitizers
US2874072 *Sep 17, 1956Feb 17, 1959Gen ElectricAutocatalytic copper plating process and solution
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3268422 *Mar 25, 1964Aug 23, 1966Nat Steel CorpElectroplating bath containing aluminum and manganese-bearing materials and method of forming aluminummanganese alloy coatings on metallic bases
US3303029 *Jan 23, 1964Feb 7, 1967Shipley CoTin coating of copper surfaces by replacement plating
US3403035 *Jun 24, 1964Sep 24, 1968Process Res CompanyProcess for stabilizing autocatalytic metal plating solutions
US4265943 *Nov 27, 1978May 5, 1981Macdermid IncorporatedMethod and composition for continuous electroless copper deposition using a hypophosphite reducing agent in the presence of cobalt or nickel ions
US4272570 *Apr 11, 1980Jun 9, 1981Sunbeam CorporationProvision of surface layers of copper or copper alloyed with zinc on die castings of zinc or zinc alloys
US4325990 *May 12, 1980Apr 20, 1982Macdermid IncorporatedElectroless copper deposition solutions with hypophosphite reducing agent
US4576689 *Apr 25, 1980Mar 18, 1986Makkaev Almaxud MCopper salt, hypophosphite, stabilizer
US5523174 *Apr 10, 1995Jun 4, 1996Ibiden Co., Ltd.Printed circuit boards
US5827604 *Dec 1, 1995Oct 27, 1998Ibiden Co., Ltd.Multilayer printed circuit board and method of producing the same
US7828872 *Aug 18, 2005Nov 9, 2010Ishihara Sangyo Kaisha, Ltd.mixing divalent copper oxide with a reducing agent (hydrazine hydrate) in the presence of a complexing agent (butylamine, edta, citric acid ), a protective colloid ( gelatin ) in a liquid medium to produce copper microparticles without formation of a univalent copper oxide from the divalent copper oxide
DE1300762B *Mar 23, 1965Aug 7, 1969Kampschulte & Cie Dr WAlkalische Loesung und Verfahren zum Abscheiden von Kupfer auf Nichtleitern
DE2715850A1 *Apr 6, 1977Oct 13, 1977Kollmorgen Tech CorpVerfahren zum abscheiden von kupfer oder kupferlegierungen aus stromlos arbeitenden baedern
DE2920766A1 *May 22, 1979Nov 29, 1979Macdermid IncLoesung und verfahren zur stromlosen kupferabscheidung unter verwendung eines hypophosphit-reduktionsmittels
DE3045281C2 *Apr 25, 1980Mar 8, 1984Institut Fiziko-Chimiceskich Osnov Pererabotki Mineral'nogo Syr'ja Sibirskogo OLoesung und verfahren zur elektrochemischen metallisierung von dielektrika
Classifications
U.S. Classification427/437, 106/1.26
International ClassificationC23C18/31, C23C18/40
Cooperative ClassificationC23C18/40
European ClassificationC23C18/40