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Publication numberUS3309293 A
Publication typeGrant
Publication dateMar 14, 1967
Filing dateNov 16, 1964
Priority dateNov 16, 1964
Publication numberUS 3309293 A, US 3309293A, US-A-3309293, US3309293 A, US3309293A
InventorsNobel Fred I, Ostrow Barnet D
Original AssigneeElechem Corp
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Copper cyanide electroplating bath
US 3309293 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

3,309,293 COPPER CYANIDE ELECTROPLATING BATH Barnet D. Ostrow and Fred 1. Nobel, Roslyn, N.Y., assignors to Elechem Corp., Jersey City, N.J., a corporation of New Jersey N Drawing. Filed Nov. 16, 1964, Ser. No. 411,543

4 Claims. (Cl. 204-52) This application is a continuation-in-part of co-pending application Ser. No. 636,862 filed Jan. 29, 1957, now abandoned, for Copper Bath With Alkylene Oxide Derivatives, which is a continuation-in-part of Ser. No.

78,908 filed Dec. 30, 1954, now abandoned, for Copper Plating Composition.

The present invention is directed to electroplating, more particularly to an improvement in a copper cyanide plating bath whereby higher efficiency is obtained.-

The addition of surface active agents to cyanide copper baths has been proposed frequently in the past to increase the tolerance of the baths toward organic addition agents and these agents were required to be present in cornpara tively large concentrations. For example, the use of alkyl betaines has been sugggested. In order to overcome the adverse effects of water breaks inherent in thesematerials, cationic quaternary ammonium chloride compounds were incorporated therewith.

The concentration of betaine to be effective was comparatively high, the minimum being .075 gram per liter. The tolerance thereof to organic compounds was low, and the rinsability of the coating was far from that desired. Also, the brightening effect was only moderate.

The present invention is intended to overcome the deficiencies of the prior art, it being among the objects thereof to provide an additive to a cyanide copper plating bath which will not only impart improved brightness thereto, but will also be effective in the low current density areas.

It is also among the objects of the invention to introduce such an additive which will give better rinsability with little or no tendency for water breaking, have greater tolerance to organic contamination, and be compatible with other bath additives.

It is further among the objects to provide a substance which will act as an improved hydrotrope when used in conjunction with other wetting agents and will show synergistic effects.

In practicing the invention, there is added to the bath a compound of the following general formula, that is a sulfobetaine:

wherein R is CH (CH and the CH chain may have some unsaturated radicals, having y carbon atoms, and y is to 25. R and R are the same or different radicals taken from the class of H and-alkyl and hydroxy alkyl having 1 to 4 carbon atoms,-n is 1 to 6.- The components include the anhydrides wherein S is linked to N through oxygen. Examples of such radicals are oleyl, myristyl, methyl, octyl, hydroxy propyl, and the like.

Such components are very active surface active wetting agents when used alone. They also improve the characteristics of other known wetting agents, including those described below.

In conjunction with such brightening agents, such as the ethylene oxide adducts, the sulfobetaines show synergistic effects. For instance, many such adducts exhibit reduced solubility in the bath and cause cloudiness at increased temperatures. Such cloudiness is greatly reduced and even completely eliminated when the sulfobetaines are added to the bath.

States Patent 0 Cyanide copper plating baths, particularly the high efliciency baths, operating with a low free cyanide content, are desirable for improved and broader bright current density range and higher efficiency. However, such baths are highly sensitive to skip plating and they exhibit dullness in the low current density range when contaminated with organic substances. The prior carboxy betaines and carboxy acids do not improve the brightness in the low current density areas to any such extent as the sulfobetaines under equivalent conditions.

In cyanide copper plating, numerous metallic addition agents are used to help brighten the deposit. Some of the metallics which have been proposed are the soluble salts of lead, antimony, bismuth, thallium and arsenic. Lead, antimony and thallium have been used in conjunction with sulfur compounds such as thiocyanate or with selenium compounds. They, however, have the undesirable characteristic of occasionally causing rough deposits. Also, when the plating bath was idle, they tended to deposit on the anode by immersion and were thus removed from solution. This deposition necessitated the use of excessively large amounts of these metallics and required a period of initial electrolysis to dissolve the deposited metallic bright-- eners from the anodes in order to make them effective in the bath.

It has been found that certain surface active wetting agents when used in cyanide copper electrolytes in conjunction with certain metallic addition agents, prevent the metallics from depositing on the copper anode by immersion when the bath is idle. They thus reduce the necessity of requiring higher concentrations of these metallics .in order to be eifective and hence reduce or eliminate the tendency to cause roughness of the deposit. These wetting agents are also beneficial when used alone or in combination with each other as herein subsequently described.

The aforementioned addition agents are compounds having the following formulas wherein n is 2 to R is aryl or alkyl containing from 6 to 20 carbon atoms. R is (CH COOH where y is 1 to 6.

Of these agents, nitrogen containing compounds are preferred to the others, although a beneficial effect upon the bath is produced by the use of any one or more.

Many of the aforementioned compounds can be used in small concentrations, for example .001 to .01 gram per liter, and still remain effective. It is true, however, that under certain conditions higher concentrations may be required or desired and are not harmful. These concentrations may go up to the limit of solubility of the particular compound used. Since these materials have the characteristic of increasing the tolerance of the cyanide copper bath to organic contamination, they may also be used in higher concentrations to overcome the effect of organic contamination in addition to having the beneficial effect referred to above on the heavy metals. However, with very high concentrations, many of these ethylene oxide condensates tend to cloud or even salt out under the operating conditions of the cyanide copper baths and thus tend to limit the concentration which can effectively remain in solution.

It has been found that by incorporating with these ethylene oxide compounds small amounts of ampholytic surface active agents or anionic wetting agents, a reduction in the clouding tendency is obtained, permitting the use of larger amounts of these condensates. By ampholytic compounds is meant those compounds which have the property of dissociation in either acid or basic media. The ampholytic compounds which have been found satisfactory for the use described in the foregoing paragraphs are as follows:

8 RNHR R is aryl or alkyl containing from 6 to 20 carbon atoms. R is (CH .SO H, wherein y is 1 to 6.

It is also possible using the modified ethylene oxide compound 7 to provide additives which do not readily cloud when used in high concentrations in the bath without impairing the beneficial effect thereof on the heavy metal addition agents.

These modified compounds have an improved cloud point, impart brightness to the cyanide copper baths and still maintain the desirable property of reacting with heavy metal addition agents. These ethylene oxide-carboxy acid ampholytes of Example 7 and the sulfonic ampholytes of Example 8 are also effective brighteners in the cyanide copper baths and are completely stable under all normal conditions of operation.

In view of the disadvantages inherent in prior art additives, the present invention overcomes practically all of the defects above noted. Applicants have obtained superior brightening of the deposits and particularly so in the low current density areas. They obtain better rinsability of the work, and have eliminated the tendency to water breaking. The additives produce greater tolerance to the presence of contaminants of organic nature. When used in conjunction with other wetting agents they act as improved hydrotropes. Our baths are notably effective to give excellent results in low free cyanide baths. The baths are not subject to skip plating.

The following examples will serve to further illustrate this invention, the conditions of operation being the same as for the standard cyanide copper bath, the amounts being grams per liter (g./l.). The conditions of operation are those ordinarily used in Hull cell operation. A temperature of about 140 to 180 F. is used with a current density of about 10 to 60 amperes per square foot. Plating is conducted for 10 minutes with continuous agitation:

Example 1 CuCN 6O KCN 90 KOH 3O Rochelle salts 45 T1 as a soluble salt .007 Se as K Se .004 Lauryl amine of polyethylene glycol 660 .02 Sodium ethyl taurate of lauryl amine .08

Example 2 CuCN 60.0 KCN 95.0 KOH 30.0 Rochelle salts 25.0 C H OPO (C H O) H 0.15 Se as K SeO 0.3 Lauryl sulfobetaine 0.2

Example 3 CuCN 45.0 KCN 83.0 KOH 30.0

Decylamine sodium ethyltaurate 0.25

Sodium acetate of lauryl amine polyethylene glycol 660 (C H N(C H O) H)CH.COONa 0.25

Example 5 CuCN 60 KCN KOH 30 KCNS 15 Sb as tartrate 008 Lauryl diethylenetriamine of polyethylene glycol 800 0.1

Lauryl dimethyl sulfobetaine 0.5

Example 6 CuCN 60 KCN 95 KOH 30 KCNS 15 Sb as tartrate .008 Lau'ryl thioether of polypropylene glycol 1000 .05 Lauryl amine sulfoacetate 0.4

Example 7 Copper cyanide 60.0 Free KCN 12.0

KOH 45.0

NaCNS 15.0

KSb Tartrate 0.02

Cetyldimethyl sulfobetaine 0.3

Example 8 Copper Cyanide 45.0 Free KCN 10.0

K Tartrate 45.0

Selenourea .003

Pb acetate .004 Nonyl ether of polyethylene glycol 2000 0.20 O'leyldimethyl sulfo betaine 0.1

Example 9 CuCN 60 KCN 95 KOH 25 Rochelle salts 30 Se as selenourela .003 Methyl, hydroxyethyl, cetyl su'lfob'etaine 1.0

Example 10 CuCN 45 KCN 70 KOH 15 Rochelle salts 30 Se as potassium selenosulfite .005 Sodium methyl taurateof decylamine 0.2

Example 11 CuCN 60 KCN KOH 30 Potassium citrate 30 Dimethyl, lauryl sulfobetaine .03

While only a certain number of specific embodiments of this invention have been described, nevertheless this invention is not limited thereto and such changes as may be apparent to one skilled in the art may be made Without departing from the spirit thereof. Furthermore, this specification is to be broadly construed and not to be limited except by the character of the claims appended hereto.

In the claims there are listed a number of sulfonic acids. These may be introduced or used in the form of the soluble salts thereof. Such salts are formed in the alkaline baths when the free acids are added.

What is claimed is:

1. In an aqueous alkaline cyanide copper plating bath, the improvement which comprises the addition to said bath of RNH(OH SO X; in the amount of 0.001 g/l. to the limit of solubility and wherein R is a radical selected from the group consisting of alkyl radicals having 6 to 20 carbon atoms, X is H or alkali metal, and y is 1 to 6.

2. In an aqueous alkaline cyanide copper plating bath, the improvement which comprises the addition to said bath of at least one compound selected from the group consisting of wherein y is 1 to 6; R is a radical selected from the group consisting of aliphatic chains having 6 to 20 carbon atoms; and R and R are radicals selected from the group consisting of alkyl having 1 to 4 carbon atoms; the amount of said additive being from 0.001 g/l. to the limit of solubility.

3. An alkaline cyanide copper bath according to claim 2, characterized in that it contains polyglycol ethers hav- 6 ing surface activity, said ethers having 2 to 100 ethoxy groups.

4. An alkaline cyanide copper bath according to claim 1, characterized in that there is also present an agent which is selected from the group consisting of an ethoxylated alcohol amine and thio-alcohol.

References Cited by the Examiner UNITED STATES PATENTS 20 JOHN H. MACK, Primary Examiner.

ALLEN B. CURTIS, Examiner.

G. KAPLAN, Assistant Examiner.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2255057 *Oct 2, 1939Sep 9, 1941Du PontElectroplating copper
US2541700 *Feb 28, 1946Feb 13, 1951Du PontElectroplating copper
US2765269 *Nov 19, 1954Oct 2, 1956Barnet D OstrowBath for plating bright gold
US2817627 *Jul 11, 1955Dec 24, 1957Nobel Fred IProcess for plating bright brass
US2828252 *Apr 23, 1954Mar 25, 1958DegussaElectrodeposition of bright zinc, copper, or nickel
US2848394 *May 4, 1956Aug 19, 1958Hanson Van Winkle Munning CoBright copper plating
US2873234 *Jun 19, 1957Feb 10, 1959Metal & Thermit CorpElectrodeposition of copper
US2873235 *Jun 19, 1957Feb 10, 1959Metal & Thermit CorpElectrodeposition of copper
US3111465 *Feb 9, 1959Nov 19, 1963M & T Chemicals IncElectrodeposition of copper and copper alloys
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4376685 *Jun 24, 1981Mar 15, 1983M&T Chemicals Inc.Acid copper electroplating baths containing brightening and leveling additives
U.S. Classification205/293, 205/298, 205/296
International ClassificationC25D3/40, C25D3/38
Cooperative ClassificationC25D3/40
European ClassificationC25D3/40