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Publication numberUS2929742 A
Publication typeGrant
Publication dateMar 22, 1960
Filing dateMar 5, 1957
Priority dateMar 5, 1957
Publication numberUS 2929742 A, US 2929742A, US-A-2929742, US2929742 A, US2929742A
InventorsAbner Brenner, De Minjer Clara Hinderina
Original AssigneeAbner Brenner, De Minjer Clara Hinderina
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Electroless deposition of nickel
US 2929742 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

c. H. DE MINJER ETAL 2,929,742

ELECTROLESS DEPOSITION OF NICKEL Filed March 5, 1957 March 22, 1960 (ADM/UM CHLORIDE 4 CONCEN TRAT/ON, Mg/L/TER SELEN/C AC/D g 5 Q E L I I I I I I 3 E8. E & 2 w

Q15 5? INVENTORS 3 E Clara H deMz'rz eP r Abner Brenner United States ELECTROLESS DEPOSITION F NICKEL Clara Hinderina de Minjer, Eindhoven, Netherlands, and Abner Brenner, Chevy Chase, Md., assignors to the United States of America as represented by the Secretary of Commerce Application March 5, 1957, Serial No. 644,171

' 1 Claim. or. 117-130 This invention relates to an improvement in the electroless plating of metals and particularly contemplates an improved process for the plating of metallic surfaces 2,532,283, issued to Brenner and Riddell, and in the following references: NBS Jour. of Research 37, pp. 1-4, 1946; Proc. of the Electroplaters Society 33, 16, 1946; NBS Jour. of Research 39, pp. 385-395, 1947; Proc. of Amer. Elec. 34, pp. 156, 1947; Metal Finishing, Novemher-December 1954.

Due to the commercial adaptation of the plating process described in the above-referred-to patent and publications, it has been found that a faster rate of plating would beldesirable. The present rate of deposition is ordinarily about 0.5 mil/hr. and, under certain conditions, can be increased to about 1 mil/hr. It has also been observed that under continuous operation in accordance with the procedural methods described in the references, nickel deposits are gradually formed on the walls of the vessel employed, particularly on scratches or on areas where local overheating occurs. The present invention contemplates an improved plating bath for use in connection with electroless plating, which provides both a substantial increase in the rate of plating obtainable, and which also diminishes the tendency of the bath to deposit nickel on the walls of the container. Ancillary to such objectives, the improvements characterizing the present invention results in an improvement in :the brightness of the plated nickel.

It is accordingly an immediate object of the present invention to provide a plating bath and procedure in connection with electroless plating whereby a much greater rate of electrodeposition may be achieved. Another object of this invention is to provide an improved process and bath which will diminish the tendency for electrodeposition on the walls of the container of the vessel containing the plating bath.

Still another object of this invention is to provide an improved plating bath and method which will result in an enhanced brightness of the plating produced. I Other uses and advantages of the invention will become apparent upon reference to the specification and drawing in which the drawing shows a chart illustrating the efiects of various additives on electroless deposition in accordance with the principles of this invention.

In accordance with the principles of this invention,

ate'n'tO additions are made to the electroless platingbath defurther aid in the production of a brighter deposit.

The manner in which the above-enumerated improved results are obtained will best be understood by considering briefly the fundamentals of the reaction and certain theoretical ideas. Specifically, the principles underlying the present invention are based upon a theory developed in connection with the electrodeposition of alloys, which theory is singularly applicable to explain electroless deposition.

Briefly reviewing the principal feature of the electroless plating process described in the above references, plating is accomplished by using a bath containing either an ammoniacal or an acid solution of nickel; The basic components include metal salts; hypophosphite ion, which is the active chemical reducing agent; and a complexing agent, such as hydroxyacetate. The complexing agent serves a two-fold purpose: (1) it keeps the metal in the solution in the form of soluble complexes as the pH goes up, and it also serves as a butter to keep the pH of the bath from changing too rapidly during the plating operation. The basic chemical reaction involved in the process according to the reference patent are as follows:

by weight, a hypophosphite radical of from 0.07 to 7.5 parts by weight and from 50 to 98 parts by weight of water. As fully explained in US. Patent No. 2,532,283,.

the process can be carried out in a pH range varying from 2 to 11; an acid bath being obtained by employing a sodium salt'of a weak organic acid such as sodium acetate, sodium citrate or sodium hydroxyacetate. and an alkaline bath being accomplished by employing ammonium hydroxide and a salt of a hydroxyl organic acid such as sodium citrate, tartaric acid etc.

Reaction 1 provides the deposition of metal. In this reaction an acid is formed, hence the need of buffers in the solution and the need for adding alkali to the bath as it operates. The second enumerated reaction occurs concurrently with the first and represents a waste of reducing power. The deposition of nickel is about 37% eflicient, based on the utilization of hypophosphite. This means that, under the most efficient conditions of deposition, about 5 pounds of sodium hypophosphite are required to produce one pound of nickel.

Returning to a consideration of the above-referred-to theory, it is hypothesized that nickel ion is not directly reduced by hypophosphite. Electroless plating involves two steps which occur almost simultaneously: (1) The discharge of hydrogen; (2) induced deposition of nickel. The mechanism of the latter is assumed to be activation of nickel ions by the excess energy of the hydrogen discharge, which activation enables the nickel ions to react with the hypophosphite ions.

Still in accordance with such theory, one equivalent of hydrogen on discharging can bring about the activation of not more than one equivalent of nickel ions, so that the maximum theoretical efficiency of nickel deposition, based on the consumption of hypophosphite, is 50%. Such theory is in accord with the known fact that the eificiency of metal in deposition is never above 40%.

The theory is of particular value in explaining the efiect of variables, such as the nature of the metal surface on which deposition is to be made, temperature,

and the presence of addition agents on the efliciency and- According to the theory, if'a metallic surface has too high a; hydrogen overvoltage, the chemical energy of the hypophosphite reaction may be insuflicient to bring about the discharge of hydrogen. Consequently,- the aboveenumerated step 2), which involves;nickekdeposition, would not occur. Conversely, a lowering'of. theovervoltage on the, catalytic metal surface. should increasehthe rate of discharge of hydrogen, butthis wouldnotnecessaril'y lead to an increase in the rate. of deposition of nickel. If it is assumed that a certainamountaofexcess energy of hydrogen discharge is necessary in electroless plating to bring about the activation of nickel ions accordirig. to such step (2);,then if the overvoltage: is too low, hydrogen may discharge. freely, and. yet not result in activation of deposition of nickel. Thus, thisdiscussion ofthe mechanism of.electrolessplatingindicates, that an optimum-hydrogen overvoltage mayin factexist.

To sumup the situation then, ,too low an overvoltage prevents activation of nickel according. to step 2), and conversely too high an overvoltage, inhibitsstep, (1) above. f

It isinteresting to note that the above-explained theory coincides with readily demonstratablephenomena; characterizing the electroless plating process. Specifically-When aroughsurface which has a lowhydrogen Overvoltage-is employed in the electroless plating bath, hydrogen; discharge. occurs freely, but Without; nickel deposition. Furthermore, it has been observed that the nickel deposition never occurs without hydrogen discharge. On the other hand, when metals of high hydrogen overvoltage such as cadmium, lead, mercury, zinc, or tin is employed hydrogen does not discharge. from. the hypophosphite solution. Consequently, electroless. nickel cannot: be directly plated over such metals, as, is wellknown. According to the premise of step (1) in the'above; theory which involves the energy of hydrogen discharge, it can be logically concluded that: (a) Substances which aifect hydrogen overvoltage also have. an efiect on;the electroless plating process and that (b) substances that normally poison electroless platingprobably act through their efiect on hydrogen overvoltage.

Onthe basis of such deductions, the present invention contemplates the addition to the electroless plating bath of various substances which affect hydrogen overvoltage. It was found that such substances which in moderate concentrations tended to act as poisons, have. in, fact several beneficial eflectson the electroless plating process when employed in low concentrations. A general class of substances which afiect hydrogen .overvoltage are the inhibitors used in the pickling treatment of steel. Small concentrations of certain substances exert a, large, effect on hydrogen overvoltage. See, for example, an article by I. William Bockris and B. Conway, Trans. of theFaraday Soc., 45, 989 (1949) and an article; by Misch and Bernstein, Jour. of Phys. Chem. 55, 1401 (19.51). Knowing the elfect of hydrogen overvoltage on the. electroless plating, process in accordance, with .the theory as explained above and with the further knowledge of the effect of certain substances on hydrogen overvoltage, a number of substances were found which when .added to the electroless bath were found to affect the rate of electroless plating even in concentrations of one. part' per million of solution. As will be indicated, some-of these substances increased the rate. ofdeposition and also stabilized the bath against spontaneous decomposition. Other substances atfected the brightness of the: deposit, in some instances making it brighter, in. others making it matt.

In general, the following substances were found to be especially eflicacious in connection with theelectroless deposition of nickel: (l) Thiourea; (2) potassiumthiocyanate; (3) selenic acid, and (4) cadmium chloride. Thechart shown in thedrawingillustratesthe effect of suchsubstances on the rate of electroless plating-for different concentrations of the. particular additive em- 4 ployed in mg. per liter. Referring to the drawing, it will be noted that thiourea has the most pronounced effect on the rate of deposition. It increases the rate of metal deposition by 50%, bringing the rate of deposition from about 1 mil to 1.5 mils per hour, a rate which compares favorably to that obtainable in conventional electrodeposition. The optimum concentration of thiourea was found to be about 0.7 mg. per liter; that is, slightly less than one part per million parts. of bath. At slightly higher concentrations, for example, several milligrams per liter, the poisoning effect of the additive compound is strongly evident as indicated by the region marked A in the drawing.

The addition of thiourea'to the electroless plating bath in the optimum concentration indicated in the drawing has another beneficial eifect on the operation of the process described in the previously-referrcd-to references. Specifically, it is eifectivein, preventing, the troublesome and hitherto. unsolved problem of-gradual, spontaneous deposition of nickel on the walls of the containing, vessel. The effectivenessof thiourea in such connection is apparently due to adsorption of the additive ,on the walls. of they vessel and on the surfaceof the. object during, plating. In addition, it was; found that the additionof thiourea also improved the brightness of the deposit.

The efiect of potassium thiocyanate. and selenic; acid on deposition is also indicated in the drawing. As-shown, such additives increase the rate of nickel deposition, but notto the extent exhibited by'thiourea. The additionof thiocyanate results in a matt deposit while selenic, acid improves the brightness .of the deposition;

As indicated inv the drawing, the efiect-of cadmium chloride as an additive tothe electroless plating; bath results in a slight decrease in the rate of plating. How- .ever, it is considered beneficial to theprocessintview of its efliect in improving the brightness of the resulting deposit. Specific embodiments of the process according to this invention are illustrated in the followingexamples.

EXAMPLE I An acid electroless nickel plating bath ispreparedin accordancewith thev teachings of the above-identified-Patout No. 2,532,283. The bath has the, following;com po.- sition:

pH 4 to 4.5.

In accordance with the teachings in the reference patent, the hypophosphite radical in the plating bath may also be secured by the use of ammonium hypophosphite or-potassium hypophosphite. To-this bath is added-thiourea, in. an amount of 1 mil per liter of'bath. Thebathis operated in a temperature range betweento l00"-jC. A steel specimen which has been previouslydegreased, is cleaned in a conventional manner dipped in hydrochloric acid, rinsed, and immersed in. the bath- Deposition of a nickel-phosphorous alloy takesplace at a rate of about 30 microns per hour which is about 50% faster than-the-ZO microns perhour rate which occurs inthe'absenceof-a thiourea additive. Noxdeposition of nickelwas observed to. form on the vessel containing the bath even after long operation of the bath.

EXAMPLE'jH,.

' An electroless plating bath as .inthe refetreditotpatcnt having the following composition is prepared:

A-selepic acid-additiveisadded in a concentrationoffi assume milligrams per liter of bath. The operation of the bath to produce deposition and the preparation of the sample is similar to that described in connection with Example I. The rate of deposition of nickel-phosphorus alloy was observed to increase about 50% over the rate of deposition from the bath without the additive. Moreover, the deposits obtained with the selenic acid additive were found to be brighter and of more uniform appearance than those obtained without the additive.

The above-described baths are exemplary and it will be apparent that the additives can also be combined with the various electroless baths specifically enumerated in Patent No. 2,532,283 above-referred-to. The various additives including potassium thiocyanate and cadminum chloride can be interchangeably employed with either of the above-exemplified baths as well as those described in the reference patent.

The influence of the above-referred-to additives when added to an acid electroless nickel bath is further detailed in the following tables.

Table 1 mg. additive per liter microns appearance per hour 21. 6 bright. 22.1 very bright. 27. 0 D0. 28. 2 Do. 29. 6 Do. 24. 8 D0. 13. 2 bright, pits.

0 no deposit.

21. 6 bright.

b i ht 3 vary 1 g 39. 9 Do. 38. 7 Do. 29.0 Do.

0. 6 very thin.

0 no deposit.

21. 6 bright. 28. 8 matt. 29. 1 Do. 27. 2 D9.

0.2 no deposit.

21. 6 bright. 21.1 Do. 17. 2 very bright. 11.5 bright. streaks.

0. 9 stained.

What is claimed is:

In an autocatalytic chemical reduction process for continuously plating nickel on metallic objects, a plating bath comprising an aqueous solution of a nickel salt, the nickel ion being present in an amount not substantially in excess of about 1 part by weight to about parts by weight of said solution, an alkaline hypophosphite, the hypophosphite radical being present in an amount not substantially in excess of about 1 part by weight to about 100 parts by weight of said solution, sodium hydroxyacetate in an amount not substantially in excess of about 5 parts by weight to about 100 parts by weight of said solution, and an additive for increasing the rate of deposition of electroless nickel, said additive consisting essentially of selenic acid in a concentration range of from 0.1 part per 1,000,000 parts to 10 parts per 1,000,000 parts of said solution.

References Cited in the file of this patent UNITED STATES PATENTS 2,762,723 Talmcy et al Sept. 11, 1956

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2762723 *Jun 3, 1953Sep 11, 1956Gen American Transporation CorProcesses of chemical nickel plating and baths therefor
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3261711 *Dec 17, 1962Jul 19, 1966Honeywell IncElectroless plating
US3268353 *Nov 18, 1960Aug 23, 1966Electrada CorpElectroless deposition and method of producing such electroless deposition
US3281266 *Apr 12, 1963Oct 25, 1966Honeywell IncElectroless plating
US3282723 *Nov 18, 1960Nov 1, 1966Electrada CorpElectroless deposition and method of producing such electroless deposition
US3353986 *Nov 20, 1963Nov 21, 1967Sperry Rand CorpElectroless deposition of cobalt-ironphosphorous magnetic material
US3515649 *May 2, 1967Jun 2, 1970Hepfer Ivan CPre-plating conditioning process
US3661596 *Apr 29, 1970May 9, 1972Schering AgStabilized, chemical nickel plating bath
US3876434 *Jan 23, 1974Apr 8, 1975Shipley CoReplenishment of electroless nickel solutions
US3971861 *Oct 25, 1974Jul 27, 1976Handy Chemicals LimitedAlloy plating system
US4005229 *Jun 23, 1975Jan 25, 1977Ppg Industries, Inc.Novel method for the rapid deposition of gold films onto non-metallic substrates at ambient temperatures
US4224133 *Dec 7, 1977Sep 23, 1980Showa Denko K.K.Cathode
US5141778 *Jan 23, 1991Aug 25, 1992Enthone, IncorporatedMethod of preparing aluminum memory disks having a smooth metal plated finish
US5523174 *Apr 10, 1995Jun 4, 1996Ibiden Co., Ltd.Printed circuit boards
US5578187 *Oct 19, 1995Nov 26, 1996Enthone-Omi, Inc.Plating process for electroless nickel on zinc die castings
US5827604 *Dec 1, 1995Oct 27, 1998Ibiden Co., Ltd.Multilayer printed circuit board and method of producing the same
Classifications
U.S. Classification427/438, 106/1.27
International ClassificationC23C18/36, C23C18/31
Cooperative ClassificationC23C18/36
European ClassificationC23C18/36