US2908568A

US2908568A - Methods of making nickel phosphorous alloys

Info

Publication number: US2908568A
Application number: US514472A
Authority: US
Inventors: William J Crehan; Walter F Klouse; Talmey Paul
Original assignee: General American Transportation Corp
Current assignee: General American Transportation Corp
Priority date: 1955-06-10
Filing date: 1955-06-10
Publication date: 1959-10-13
Anticipated expiration: 1976-10-13

Description

Oct. 13, 1959 TEM/25947095 6" W. J. CREHAN ETAL METHODS OF MAKING NICKEL PHOSPHOROUS ALLOYS l Filed June l0, 1955 JMWM9W IVIEIHODS F MAKING NICKEL PHOSPHOROUS ALLOYS William J. Crehan, Hinsdale, Walter *E Klouse, Chicago, and Paul Talmey, Barrington, lll., assignors to General American Transportation Corporation, Chicago, Ill., a corporation of New York Application June 10, 1955, Serial No. 514,472

'S Claims. (Cl. 75-170) The present invention relates to methods of making nickel-phosphorus alloys.

It is a general object of the invention to provide an improved method of making a nickel-phosphorus alloy comprising about 88 to 94% nickel and 6y to 12% phosphorus by weight and characterized by an eutectic composition comprising nickel and phosphorus constituents containing about 89% nickel and 11% phosphorus by weight and having an eutectic temperature of about 880 C.

Another object of the invention is to provide an improved method of making a nickel-phosphorus alloy of the type described, comprising less than 11% phosphorus by weight, and also characterized by the dispersion of primary nickel in the eutectic composition thereof.

Another object of the invention is to provide a method of making a nickel-phosphorus alloy from the heretofore useless stray plating that occurs in a plating system of the nickel cation-hypophosphite anion type.

Another object of lthe invention is to provide a method of making a nickel-phosphorus alloy from a spent chemical plating bath of the nickel cation-hypophosphite anion type.

Another object of the invention is to provide a method of salvaging nickel and phosphorus from a spent chemical plating bath of the nickel cation-hypophosphite anion type.

Another object of the invention is to provide an improved method of making a nickel-phosphorus alloy that involves the step of treating a chemical plating bath of the nickel cation-hypophosphite anion type to induce random decomposition thereof, followed by a step wherein the metallic precipitate that is formed in the plating bath incident to random decomposition thereof is converted into a useful nickel-phosphorus alloy.

Another object of the invention is to provide a simple method of converting the heretofore useless metallic precipitate that forms in a chemical plating bath of the nickel cation-hypophosphite anion type incident to random decomposition thereof into a useful nickel-phosphorus alloy.

The invention, both as to its organization-and method of operation, together with further objects and advantages thereof, will best be' understood by reference to the following specification taken in connection with the accompanying drawing, in which:

Figure l is a phase diagram of the nickel-phosphorus system, as far as it is pertinent to the nickel-phosphorus alloys that are produced in accordance with the present invention, and illustrating the mutual relationships among phase and temperature and composition in these nickelphosphorus alloys;

Fig. 2 is an enlarged fragmentary sectional view of a composite metal sheet embodying the present invention;

Fig. 2A is an enlarged fragmentary exploded sectional view of the elements of the composite sheet shown in Fig. 2, and illustrating a step involved in making the nited States Patent lCC same, in accordance with the method of the present invention;

Fig. 2B is an enlarged fragmentary exploded sectional view of the elements of the composite sheet shown in Fig. 2, and illustrating modified steps involved in the method of making the same;

Fig. 3 is an enlarged fragmentary sectional view of a modified form of the composite metal sheet;

Fig. 4 is an enlarged fragmentary sectional view of another modiiied form of the composite metal sheet; and

Fig. 5 is an enlarged fragmentary sectional view of a further modiiied form of the composite metal sheet.

At the outset, it is noted that in the operation of a continuous chemical nickel plating system of the character of that disclosed in U.S. Patent No. 2,658,839, granted on November 10, 1953, to Paul Talmey and William. J. Crehan, there is employed a plating bath of the nickel cation-hypophosphite anion type; and in the plating operation, nickel cations are reduced to metallic nickel and deposited upon the catalytic surface of the object undergoing the chemical nickel plating operation, and hypophosphite anions are correspondingly oxidized to phosphite anions and accumulate in the plating bath. In accordance with the method of Talmey and Crehan, the plating bath is continuously or periodically regenerated by the addition of nickel cations and hypophosphite ions, thereby to compensate the same for the depletion of [these ions resulting from the plating reactions mentioned. Also, these plating reactions in the plating bath are productive of hydrogen ions, whereby hydroxyl ions are added in the regeneration to maintain the desired pH of the plating bath. t

While this method greatly extends the useful life of the plating bath, it does not prevent the build-up of phosphite anions and alkali metal salts therein (assuming that the regeneration involves the addition of nickel sulfate, sodium hyophosphite and sodium hydroxide); whereby ultimately it is necessary to discard the plating bath, as a result of the build-up of high concentrations therein of phosphite anions, sulfate anions and sodium cations. Specifically, care must be exercised in this connection to prevent precipitation of nickel phosphite in the plating bath, since such precipitate serves as growth nuclei for the formation of metallic precipitate therein, with the resulting random decomposition of the plating bath. Speciiically, the reactions involving the formation of the metallic precipitate in the plating bath are autocatalytic; whereby the formation of any substantial metallic precipitate therein effects the total decomposition of the plating bath very quickly and throughout the body thereof entirely at random and altogether independently of the catalytic surface of the body undergoing the plating operation.

Thus, a chemical nickel plating bath becomes spent when the phosphite anion concentration therein approaches the threshold of insolubility of nickel phosphite, and must be discarded, so as to prevent the possibility of random'decomposition thereof in the plating system.

The spent chemical nickel plating bath contains valuable nickel, hypophosphite and phosphite, as well as sodium and sulfate; whereby it is ordinarily subjected to gross nickelsalvage by treatment that induces random decomposition thereof, the residue of kthe plating bath comprising an aqueous liquid having the previously mentioned metallic precipitate suspended therein. The matter of the treatment of the chemical nickel plating bath to induce random decomposition thereof is exceedingly easy, as this phenomenon involves the previously mentioned reactions that are autocatalytic; whereby lthe reactions, once initiated, -rapidly spread throughout the plating bath and proceed substantially on a quantitative basis with respect to the twoingredients (nickelcations and hypophosphite anions) with the formation therein of the metallic precipitate mentioned. Thus, all of the nickel'cations inthe plating bathare depletedinthe presence of the normal slight excess of hypophosphite anions; whereby the subsequent recovery'of. the metallic precipitate from the aqueousliquid effects the complete recovery ofthe nickel cations from the residue of the spent chemical nickel V plating bath.

The initiation ofthe reactions mentioned is also ex ceedingly simple, as it is noted that a chemical' nickel plating bath isnormally in a metastable stateY and is subject to spontaneous decomposition. Specifically, the simplest procedure of initiating the reactions is to seed the spentchemical nickel-plating bath with a small quantity of previously producedmetallic precipitate o r a small quantity of'any catalytic material in finely dividediform, such asY iron, cobalt, nickel; palladium, etc. Palladium is highly catalytic and may be employed even in theA formof' an aqueous-solution of,'a salt thereof, such as the chloride, sulfate, etc. lAlso, the reactions in the spent chemical plating bath maybe initiatedby appropriately increasing the pHthereof', by raising the temperature thereofto the boiling point, etc. Since the reactions are autocatalytic, as previouslyY noted, it` is veryconvenient, as a matter of manipulation, to initiate the same in a small quantity offthe spent chemical nickel plating bath containedin a beaker, or the like, and then return the contents of the beaker into the vat or tank containing the bulk of the spent chemical nickel plating bath, thereby seeding the reactions in the bulk of the spent chemical nickelplating bath, in an obvious manner.

Heretofore, chemical nickel platers have returned the metallic precipitate thus salvaged from spent chemical nickel plating baths to initial nickel processors; whereby such processorsin turn, haveV recovered the nickel content ofthe, metallic precipitate by smelting operations, involving reducing agents; whereby the` crude metallic nickel thus'vrecoveredhas been refined byA electrolytie operations for further use. Although, these nickel processors have been informed of theA factthat the metajllcprecipitate thus salvaged from aspent chemical nickel plating bath also contains substantialphosphorus, theyI have always treated this containedphosphorus as just another impurity encountered inl the smelting of nickel ores; whereby the phosphorus content of` the metallic precipitate has been totally wasted in these srnelting` operations.

Perhapsthe primary reason for this gross salvage of only` the nickel ingredient of this metallic precipitate by the nickel processors has been a total misconception of the fundamental character and composition thereof. Recently, this metallic precipitate has been discovered to bean/amorphous solid comprsingla metastable undercooled solution of phosphorus in nickel, and havingno specliic composition, but normally containing, yas produced incident to the Vrandom decomposition i, of a `chemal nikelplatingbath of the nickel cation. hypophosphlte aniontype, constituents comprisingY aboutI 88 -to phosphorus content, is.aifectedbytheexcessof both hypophosphite anionsand phosphite anions inth espent;

Phiteaniqns in; the. spent ,chemicalnickeliplating vbath is byfnoqmsensx essentielle thefrzroductin-0t a high Lphos: phprusfcontentirl-,the rne'tallc-.r ,rffQinitate` In. factth e mtteHiQprinifate produced-*incident ,to therandom. de.- composition of a pure simple freshly prepared standard '60 94% nickeland 6 to 12% phosphorus by weight. The

aqueous solution of nickel sulfate and sodium hypo phosphite always contains phosphorus in the range 6 to 12% by weight, frequently has a phosphorus content as high as 10% by weight, and occasionally has a phosphorus content as high as 12% by weight. This phenomenon is not really understood, as the random decomposition of thek same standard solution in two separate batches is not necessarily productive of identical samples ofV metallic precipitate, as to phosphorus content. It is suggested that the average character of the ultimately produced metallic precipitate may be greatly inuenced by the character of the iirst few nuclei of the metallic precipitate that form in the solution, since the reaction is autocatalytic, and the character of these lirst few nuclei may dependl entirely uponprobability, within a very narrow range of permissible character.

Next, it has been discovered that when this metallic precipitate isv heatedtoia temperatureof about 400 C. an irreversible structural changey occurs therethrough in an exceedingly short time interval, wherebythe phosphorus that was in `solution inthe nickel reacts with the nickel toproduce nickel phosphide (Nial), which latter compound is dispersed inthe form of micro-crystals in a matrix of nickel in the resulting mass. Asthe temperatureo this resultingvmass is elevated, the Nisly crystals growinthe-nickel matrix untiliultimately a melt trated a portion of the nickel-phosphorus system thatV is4 pertinent to.V the nickel-phosphorus compositions produced by the'meltingof the metallic-precipitate noted. Specilically, itA was discovered. that the eutectie comlposition comprises nickel and` phosphorus constituents.

containing about, 89% nickel and 11% phosphorus. by weight,- and that the'eutectic temperature is about 880 C. On the curve 1711, the melting point of nickel (1453 C.) is indicated at 12, and the eutectic point'isY indicated at 13 Also, from the curve 11, itwill bel observed-that a composition containing about 5% phosphorus has amelting pointl of-'about- 1150 C., a-composition containing about 6% phosphorus has a meltingpoint of about-1100 C., acomposition containingabout 10% phosphorus-has a-melting point of about 950 C., and acomposition containing about|12% phosphorus-has a melting point ofvabout-950YJ C.

Thefeutectic composition ofthe system is. not completely understood, since it appears that it involves Afundamentallynickel and NiSP, and since the proportionstby weight are not.in strict accordance with Daltons Law; however, repeated'. and accurate analysisalways yields thisratio ofnickel .and .phosphorus by weight, and only nickel and Nial. have been detectedin the. alloy.

Alll of` thefcomposition that, are produced. by melting ofthe; metallic precipitatenoted'contain nickel and phosphorus in the previously mentioned range byA weight (about 881949Z nickel and 6-12% phosphorus); and

most of the. compositions fall in the even more'limited.

range containing about f93% nickeland,7-10% phosphorus byweight. Thus, it will be understood thatwhen the metallic precipitate is heated to a temperaturesuiciently high-to melt thel same, a melt` is produced in which the nickel'. and phosphorusconstitucnts. are in equilibrium above the curve 11, of the phase diagram of Fig. 1. Upon subsequent. cooling, the melt becomes super-saturated with nickel in the event the phosphorus content of the composition is below 11%; whereas upon subsequent cooling, the melt becomes supersaturated with Ni3P- in the event the phosphorus content of-the composition is above., 11%. Specically, in the event there isadeciency of phosphorus the melt becomes supersaturated-with nickel, upon subsequent cooling; whereby solid nickel is formed in the solution of the eutectic as the composition of the solution moves downwardly and toward the right along the curve 11 and toward the eutectic point 13; hence, when the cooling of the melt proceeds to the eutectc temperature of about 880 C. considerable solid nickel is present in the solution of the eutectic composition, so that upon further cooling of the mass, this solid nickel is productive of primary nickel crystals in the mass of the eutectic composition that appear as substantial nickel dendrites dispersed in the line crystals of nickel and Ni3P comprising the fundamental constituents of the eutectic composition. Specifically, in the event there is an excess of phosphorus, the melt be comes supersaturated with NisP, upon subsequent cooling; whereby solid Ni3P is formed in the solution of the eutectic as the composition of the solution moves downwardly and toward the left along the curve 11 and toward the eutectic point 13; hence, when the cooling of the melt proceeds to the eutectic temperature of about 880 C., considerable solid Ni3P is present in the solution of the eutectic composition, so that upon further cooling of the mass, this solid NigP is productiveof primary Nia? crystals in the mass of the eutectic composition that appear as small crystals of Ni3P dispersed in the fine crystals of nickel and Ni3P comprising the fundamental constituents of the eutectic composition. Accordingly, it is the melting of the metallic precipitate noted, followed by the subsequent cooling and solidifying of the melt, that is productive of the nickel-phosphorus alloy characterized by the eutectic composition having dispersed therein the primary crystals mentioned. As previously noted, in this metallic precipitate, there is normally an excess of nickel in the composition, whereby the nickel-phosphorus alloys produced is normally characterized by the dispersion therein of nickel dendrites.

From a broad point of View, as a matter of deiinition, the original nickel-phosphorus material resulting directly from the nickel cation-hypophosphite anion reaction (the amorphous solid material described) may be termed an alloy, although it is not characterized by the eutectic composition noted; however, it is preferable to apply the term alloy to the final nickel-phosphorus material that results from the melting and subsequent solidifying of the original material mentioned, since this nal material is characterized by the eutectic composition noted. Thus, hereinafter the term alloy will be used only to refer to this linal material.

Now this nickel-phosphorus alloy is substantiallyA different, as to characteristics and structure, from the solid nickel-phosphorus material that is chemically plated from a plating bath of the nickel cation-hypophosphite anion type and from the solid nickel-phosphorus material of the metallic precipitate. For examples, this nickel-phosphorus alloy is substantially magnetic, Whereas the nickel-phosphorus plating and the metallic precipitate are substantially non-magnetic; and the specific resistance of this nickel-phosphorus alloy is considerably less than that of the nickel-phosphorus plating or the metallic precipitate. There are also many other physical and structural differences between this nickel-phosphorus alloy and the nickel-phosphorus plating and the metallic precipitate that are not here discussed at length in the interest of brevity.

Moreover, it will be understood that while the metallic precipitate must be melted to effect the production of the nickel-phosphorus alloy described above, it is not necessary to maintain the condition of the melt for any particular time interval.

The method of making the nickel-phosphorus alloy, described above, from the spent chemical nickel plating bath not only provides an eicient scheme of salvaging valuable nickel and phosphorus therefrom, but provides an exceedingly valuable alloy having many important uses, as explained more fully hereinafter; and it is emphasized that the salvage method is applicable to a wide variety of chemical nickel plating baths, such, for example, as those disclosed in the following U.S. patents: No. 2,532,- 283, Brenner and Riddell; No. 2,658,841, Gutzeit and Krieg; and No. 2,658,842, Gutzeit and Ramirez. Thus, the chemical nickel plater may select the chemical nickel plating bath that is best suited to his particuflar operation, and subsequently subject the spent chemical nickel plating bath to salvage in accordance with the present method, and regardless of the particular composition of the chemical nickel plating bath.

A preferredchemical nickel plating bath of extremely wide utility is disclosed in the copending application of IGregoire Gutzeit, Paul Talmey and Warren G. Lee, Serial No. 479,088, tiled December 3l, 1954, now Patent No. 2,822,293, granted February 4, 1958, this particular plating bath being admirably suited to the continuous plating process disclosed in the Talrney and Crehan patent. The chemical plating bath of the Gutzeit, Talmey and Lee application mentioned essentially comprises an aqueous solution of a nickel salt, a hypophosphite, a complexing agent'seleoted from the group consisting of lactic acid and salts thereof, and an exalting additive selected from the group consisting of propionic acid and salts thereof. In this plating bath, the absolute concentration of hypophosphite is within the range 0.15 to 1.20 moles/liter, the ratio between nickel ions and hypophosphite ions is within the range 0.25 to 1.60, the absolute concentration of lactic ions is within the range 0.25 to 0.60 mole/liter, the absolute concentration of p-ropionic ions is within the range 0.025 to 0.060 mole/liter, and the pH is within the approximate range 4.0 to 5.6. v

This particular chemical nickel plating bath is most satisfactory in carrying-out a wide variety of nickel plating operations; and, of course, when it becomes spent, it may be subjected to the present salvage method to produce the nickel-phosphorus alloy previously described.

It has also been discovered that the stray plating that may occur in an undesirable manner in a chemical nickel plating system of the character of that of the Talmey and Crehan patent may also be employed in the production of the nickel-phosphorus alloy described in the general manner disclosed above. In other words, this stray plating that accumulates in the bottom of the tank in fwhich the chemical nickel plating bath is stored, in the filters of the system, etc., may be accumulated and melted in the manner described above, either alone or with the metallic precipitate mentioned, in order to produce the nickel-phosphorus alloy described. In fact, it has recently been discovered that this stray plating is also an amorphous solid comprising a metastable under-cooled solution of phosphorus in nickel, and having no specic composition, but normally containing, as produced, constituents comprising about 88 to 94% nickel and 6 to 12% phosphorus by Weight. Since the metallic precipitate mentioned and the stray plating mentioned are substantially identical, as a matter of composition, `they may be melted together in order to produce the nickel-phosphorus alloy described.

. As a matter of convenience in handling, the molten nickel-phosphorus alloy described may be cast into rods, bars, or other commercial forms, for subsequent use; whereby, such forms ofthe alloy, within themselves, comprise useful articles of convenience.

Turning now to the utility of the nickel-phosphorus alloy that is produced by the present method, it is first noted that in a molten condition, it has very pronounced wetting and bonding characteristics; whereby it is generally useful as a coating material, and may be readily applied in a great variety of ways to a vast array of different base metal bodies after they have been subjected to standard degreasing, cleaning and pickling operations. Specifically, such an alloy coating may be applied to the cleaned surface of a base metal body by any one of the following groups of steps, in accordance with the present method:

(1) The cleaned base metal body is heated, and the 7 alloy in molten condition is poured over the hot body in order to apply a cast coating of the alloy upon the body.

(2) The cleaned base metal body, at ambient temperature, is immersed in a molten mass of the alloy, and subsequently withdrawn with respect thereto, in order to apply a hot-dipped coating of the alloy upon the body.

(3) A mass of the alloy, at ambient temperature and in inely divided form, is sprinkled upon the cleaned surface of the base metal body, the body having been previously heated to a high temperature, in order to apply a melted coating of the alloy upon the body.

(4) A mass of the alloy, at ambient temperature and in nely divided form, is placed upon ythe cleaned surface of the base metal body, at ambient temperature, and the body and the carried alloy are transferred to a furnace or oven and heated, in order to apply an oven melted coating of the alloy upon the body.

(5) A portion of a bar of the alloy is melted with a torch, or the like, onto the heated and cleaned surface of the base metal body, in order to apply a tinned coating of the alloy upon the body.

(6) A mass of the metallic precipitate, or the stray plating in finely divided form, is sprinkled upon the cleaned surface of the base metal body, the body having been previously heated to a high temperature, in order to melt the mass, whereby upon subsequent cooling and solidifying of the melt, the alloy coating is formed in situ upon the body.

(7) A mass of the metallic precipitate, or the stray plating in finely divided form, is placed upon the cleaned surface of the base metal body, at ambient temperature, and the body and the carried mass are transferred to a furnace or oven and heated in order to melt the mass, whereby upon subsequent cooling and solidifying of the melt, the alloy coating is formed in situ upon the body.

(8) A portion of a bar of the compressed metallic precipitate, or the stray plating, is melted with a torch, or the like, onto the heated and cleaned surface of the base metal body; whereby upon subsequent cooling and solidifying of the melt, the alloy coating is formed in situ upon the body.

The foregoing suggestions are merely illustrative of the many ways'in which the previously prepared alloy may be applied as a coating upon a body and in which the alloy may be made in situ from the melted metallic precipitate, or the stray plating, applied as a coating upon a body; and many other modes of producing such coatings will be immediately apparent to those skilled in the tinning, soldering, brazing, galvanizing and other metalcoating arts.

Turning now to the character of -the base metal of the body that may be coated with this alloy, it is noted that the only limitation that has been discovered is that it must have a metling point sufficiently high that it is not appreciably melted in contact with the molten alloy at a temperature in the general range 880 C. to 1100 C., as the molten alloy must be heated to a temperature in this general range to obtain the desired liquid condition thereof. Also, the alloy in molten condition must wet and bond with respect to the cleaned surface of the base metal, but this condition does not comprise a substantial limitation, as the wetting and bonding characteristics of the molten alloy are outstanding; whereby even chromealloys and aluminum alloys are readily wet and bonded thereby. These peculiar wetting and bonding characteristics of the molten alloy are believed to flow from the circumstance that the phosphorus constituents of the melt are capable of reducing chromic oxide, as well as the various oxides of alumimun. In any case and without reference to the exact mechanism involved, the wetting and bonding characteristics of this nickel-phosphorus alloy are unusual; whereby there is no difficulty in proy ducing satisfactory coatings upon the cleaned surfaces of a great variety of bodies formed of base metals, precious metals, or alloys thereof; which coatings are useful either as final protective coatings for the bodies thus coated or as uniting layers employed in securing such bodies to still other such bodies.

As a matter of fact, the present method removes a limitation with respect to the conventional chemical nickel plating process and concerning the catalytic character of the base metal. More particularly, in order to obtain plating upon the cleaned surface of a base metal from a chemical nickel plating bath of the nickel cation-hypophc-sphite anion type, the surface of the base metal must be catalytic to the plating reactions involved, so as to bring about the chemical reduction of the nickel cations and the deposition of the resulting metallic nickel, and the companion oxidation of hypophosphite anions to phosphite anions; all as previously explained in the Talmey and Crehan patent. However, in accordance with the present method, the nickel-phosphorus alloy has been previously produced, or is produced in situ incident to the c ooling and solidifying ofthe melted metallic precipitate, or the stray plating; whereby it is not critical that the cleaned surface of the base metal be catalytic in order to obtain a coating thereon with the previously produced alloy, or the alloy thus produced in situ.

This method of coating the base metal body with this nickel-phosphorus alloy is disclosed and claimed in the copending application of William J. Crehan, Walter F. Klouse and Paul Talmey, Serial No. 678,683, iiled August 16, 1957.

Referring now to Fig. 2 of the drawings, there is illustrated a composite metal sheet 21, embodying the features of the present invention, and comprising an intermediate sheet 22 formed of base metal, two

outside sheets

23 and 24 formed of chrome-steel and two uniting layers 25a and ZSb formed of nickel-phosphorus alloy, the alloy layer 25a being disposed between and intimately bonded to the adjacent surfaces of the

sheets

22 and 23, and the layer 25b being disposed between and intimately bonded to the adjacent surfaces of the

sheets

22 and 24.

The nickel-phosphorus alloy of the layers 25a and 25h contains about 88 to 94% nickel and 6 to 12% phosphorus by weight and comprises the eutectic composition mentioned including nickel and phosphorus constituents containing about 89% nickel and 11% phosphorus by weight, and having an eutectic temperature of about 880 C. Since the alloy ordinarily contains excess nickel with respect to the eutectic composition thereof, ordinarily, it has a melting point somewhat above the eutectic temperature and disposed in the approximate range 880 C. to 1100 C., depending upon the composition thereof. More particularly, this alloyis that which is automatically produced bythe melting of the metallic precipitate, or by the melting of the stray plating, followed by cooling and solidifying of the melt, as previously described.

Turning now to the method of making the composite metal sheet 21, in accordance with the present invention, and referring to Fig. 2A, it is noted that all of the surfaces of the

individual sheets

22, 23 and 24 are first thoroughly degreased, cleaned and lightly pickled in a suitable acid, such as hydrochloric acid; and then the alloy coating 25 is applied to the cleaned exterior surfaces of the sheet 22 in any suitable manner and as previously described. The alloy coating 2S is intimately bonded to the surfaces of the intermediate sheet 22 and comprises the two face portions 25a and 25b respectively carried by the two faces of the intermediate sheet 22 and the two edge portions 25C respectively carried by the two edges of the intermediate sheet 22.

For example, the alloy coating 25 may be applied to the cleaned surfaces of the base metal sheet 22 by a hot dipping" step and involving the immersion of the sheet 22 for a suitable time interval in a molten mass of the alloy.

Next, the

sheets

22, 23 and 24 are stacked so that the 9 face portions 25a and 2517 of the layer 25 are disposed in respective engagements with the adjacent cleaned face surfaces of the

outer sheets

23 and 24. The edges of the

sheets

22, 23 and 24 may be tack-welded, if desired, in an obvious manner, not shown, in order to secure together the assembly, prior to fusion of the layer 25', and in order to facilitate handling of the assembly.

Then the assembly is subjected to heat and pressure in order to eifect selective Vfusion of the layer 25'; whereby the face portions 25a and 25b thereof respectively produce corresponding melts that are forced into wetting and bonding relation with the respective cleaned face surfaces of the

outer sheets

23 and 24 in contact therewith, and also into wetting and bonding relation with the respective face surfaces of the intermediate sheet 22, in order to unite the assembly.

The assembly may be heated to eifect the selective melting of the layer 25 in a furnace or oven; and it is preferable that the oven contain an inert atmosphere, such as nitrogen, as the assembly must be heated to a temperature in the approximate range 880 C. to 1100 C., in order to melt the layer 25', the melting point of this nickel-phorphorus alloy being in this general range and being variable depending upon the composition thereof. As previously explained, the required pressure may be effected upon the assembly in any suitable manner. For example, the assembly may be transferred from the oven upon melting of the layer 25', to a suitable press; whereby the assembly is retained under pressure until the melts cool and solidify, uniting the

individual sheets

22, 23 and 24.

Alternatively, when the

Asheets

22, 23 and 24 are relatively narrow, so that they comprise what may be termed strips, the heating and pressing steps may be conveniently combined in a single step by utilizing an electric resistance welding machine of the conventional rollerelectrode type. In this operation, the assembly is passing between the two opposed roller-electrodes of the welding machine, so that the required pressure is exerted therebetween upon the stack of the individual sheets of the assembly; and simultaneously a substantial electric current is passed between the two roller-electrodes and through the assembly, so that the required heating of the face portions 25a and 251; of the layer 25 is effected. This combined step `is well-suited to the method, since the face portions 25a and 25b of the layer 25 each has a high specific electrical resistance with respect to that of any one of the

individual sheets

22, 23 and 24, so that the electric heating is preferentially concentrated in the face portions 25a and 25b of the layer 25.

After cooling of the assembly, the edges thereof are trimmed to remove the surplus alloy, etc., thereby producing the finished composite metal sheet 21, as shown in Fig. 2.

In the foregoing description of the composite metal sheet 21, and the method of making the same, it has been assumed that the

individual elements

22, 23 and 24 are sheets of the required thickness to produce the nished composite sheet 21 of the required structure upon the uniting of the

individual elements

22, 23 and 24; however, this preferred form of the method is not essential thereto, as the

individual elements

22, 23 and 24 may be of such thickness that they comprise slabs, so that the united assembly comprises a billet. In this case, the billet thus produced may be subjected to subsequent working operations, such as hot or cold rolling, forging, etc., to produce the composite metal sheet 21 of the required thickness. For example, in the inished structure 21 of Fig. 2, the total thickness may be 250- mils, the element 22 having a thickness of 20G-mils, and each of the

elements

23 and 24 having a thickness of ZS-mils.

Y In the foregoingdescription of the method of making the composite metal sheet 2'1, it was assumed that the continuous coating 25 of nickel-phosphorus alloy was iirst applied to the intermediate sheet 22 before the stack-1` ing of the

individual sheets

22, 23 and 24 in order to produce the assemblyto be subsequently worked to effect the uniting thereof; all as described in conjunction with Fig. 2A. However, as an alternative method, the

individual sheets

22, 23 and 24' may be stacked with the alloy of the metallic precipitate or the stray plating layers 25a and 2511 respectively carried by the

individual sheets

22 and 24 in producing the assembly, and before further working to effect uniting. In this regard, the layer 25h may be first placed upon the cleaned upper face of the outside sheet 24 in the form of the metallic precipitate, or the stray plating in nely divided form, containing the nickel and phosphorus constituents, and before the production of the nickel-phosphorus alloy. Then the intermediate sheet 22 may be stacked upon the layer 25b, with the lower cleaned surface thereof in direct contact therewith. Then the layer 25a of previously produced nickel-phosphorus alloy in finely divided form may be placed upon the cleaned upper face of the intermediate sheet 22; and then the outer sheet 23 may be stacked upon the layer 25a with the lower cleaned surface thereof in direct contact therewith. Finally, the edges of the

sheets

22, 23 and 24 may be suitably secured together in order to retain the assembly in place preceding further working.

In this case, when the assembly is subjected to heat and pressure, in the manner previously explained, the layer 25a of iinely `divided nickel-phosphorus alloy produces a corresponding melt, while the layer 2Sb of metallic precipitate, or stray plating in nely divided form, produces a corresponding melt and is converted into the nickel-phosphorus alloy upon cooling and solidifying, in the manner previouslyexplained. This alternative procedure within itself comprises alternative procedures, as it is apparent that the layer disposed between each two of the

sheets

22, 23 and 24 may comprise either the previously produced nickel-phosphorus alloy in iinely divided form or the metallic precipitate, or the stray plating in finely divided form. Accordingly, it will be understood that in the eventthe layer disposed between two of the sheets comprises nickel-phosphorus alloy in iinely divided lform, only melting of the previously produced alloy is involved. On the other hand, in the event the layer disposed between two of the sheets comprises the metallic precipitate, or the stray plating in inely divided form, both melting and alloying of the nickel and phosphorus constituents are involved. However, in any case, the ultimate result is the same that there is provided a uniting layer of nickel-phosphorus alloy between the two sheets.

Also, in the foregoing description of the composite metal. sheet 21, and the method of making the same, it has been assumed that it is desirable to produce a structure in which both Sides of a base metal sheet are cladded by chrome-steel sheets; however, this structure of the composite metal sheet 21, as shown in Fig. 2, is unusual and was selected only for the purpose of illustrating the broad application of the present method. More particularly, it is ordinarily necessary to eect cladding of only one side of a base metal sheet; whereby the composite metal sheet 31 of Fig. 3 comprises the common form of the structure embodying the present invention. Speciically, the composite metal sheet 31 comprises a base metal sheet 34, a chrome-steel sheet l33, and an intermediate uniting layer of nickel-phosphorus alloy 35a.

The method of making the composite metal sheet 31 is the same as that described in the making of the composite metal sheet '21 and is not repeated in the interest of brevity.

Referring now to Fig. 4, another modied form of the composite metal sheet 41 is illustrated that comprises two identical

base metal sheets

43 and 44 and an intermediate uniting layer 45a of nickel-phosphorus alloy; and referring lto Fig. 5, a further modiiied form of the composite metal sheet ,-51 is illustrated that comprises two identical kchrome-steel sheets '3 and 54, and an intermediate uniting layer 55a of nickel-phosphorus alloy. The composite metal sheets 41 and f51 are also made in accordance with the present method, as described above, in the making of the

composite metal sheets

21 and 31; whereby it will be understood'that the composite metal sheets and methods of the present invention are by no means limited to structures involving a base metal sheet that is cladded with a chrome-steel sheet. The important point in this regard resides in the fact that the present method is applicable to the making of such composite metal sheets involving one or more sheets formed of metals containing substantial chromium, in view of the usual interference of the chromium with wetting and bonding by the formation of chromic oxide upon the surface of the sheet containing any substantial amount of chromium. These melting and bonding characteristics of the nickel-phosphorus alloy are, by no means, peculiar to chromium, but are general characteristics; whereby aluminum and its alloys are readily wet and bonded by the melt, notwithstanding the usual aluminum oxides on the surface of such aluminum alloy sheets.

Reconsidering the present method, it is pointed out that the nickel-phosphorus alloy comprising the uniting layer between the two metal sheets may have been previously produced by the melting of the metallic precipitate recovered from a chemical plating bath of the nickelcation-hypophosphite anion type following random decomposition thereof, or alternatively the nickel-phosphorus alloy comprising the uniting layer between the two metal sheets may be produced in situ by the melting of the metallic precipitate mentioned, or the stray plating mentioned, and incident to the uniting of the two metal sheets.

As previously explained, there is no particular or critical limitation with regard to the composition of the metal of any one of the individual metal sheets involved in the composite metal sheet; however, as a practical matter, in the production of such composite metal sheets the most important industrial metals comprise: iron and its alloys, cobalt and its alloys, nickel and its alloys, copper and its alloys, silver and its alloys, gold and its alloys, palladium and its alloys and platinum and its alloys.

For example, in each of the

composite metal sheets

21, 31, 41 and 51, the metal of at least one of the individual sheets incorporated therein will ordinarily comprise one of the following elements or alloys: iron, carbon-steel, chrome-steel, cobalt-steel, silicon-steel, manganese-steel, nickel-steel, molybdenum-steel, nickel-cobaltsteel, nickel-chrome-steel, chrome-manganese-stcel, manganese-molybdenum-steel, chrome-copper-nickel-steel, copper, brass, bronze, silicon-bronze, phosphor-bronze, beryllium-copper, cadmium-copper, chromium-copper, nickel-copper, aluminum, aluminum-brass, aluminumbronze, silver, palladium-silver, nickel-silver, coppersilver, zinc-copper-silver, Zinc-cadmium-copper-silver, gold, copper-gold, copper-silver-platinum-gold, coppersilver-palladium-gold, platinum, gold-platinum, silverplatinum, iridium-platinum, rhodium-platinum, palladium-platinum, tungsten-platinum, nickel-platinum, ruthenium-platinum, gold-silver-platinum, palladium-goldplatinum, palladium, copper-gold-palladium, nickel, chromium-nickel, and cobalt.

Thus, the cladding arrangement is of exceedingly wide utility, embracing the cladding of base metals with the full range of stainless steels, with silver (of the general character of Shefeld plate), etc. This method of making composite metal sheets employing this nickel-phosphorus alloy is disclosed and claimed in the Ypreviously mentioned application of Crehan, Klouse and Talmey, Serial No. 678,683, led August 16, 1957.

in view of the foregoing, it is apparent that there has been provided an improved method of salvaging spent chemical plating bath of the nickel cation-hypophosphite anion type in order to effect the recovery therefrom of valuable nickel and phosphoruswith the ultimate production of a valuable nickel-phosphorus alloy from the recovered constituents mentioned. Also, there has been provided an improved method of making a nickel-phosphorus alloy involving the constituents of the metallic precipitate that forms in a chemical nickel plating bath of the character noted incident to the random decomposition thereof, or the constituents of the stray plating in a plating bath of the character noted.

While there has been described what is at present considered to be the preferred embodiment of the invention, it will be understood that various modifications may be made therein, and it is intended to cover in the appended claims all such modilications as fall within the true spirit and scope of the invention.

What is claimed is:

1. The Vmethod of making a nickel-phosphorus alloy from a spent chemical plating bath containing nickel cations and hypophosphite anions and phosphite anions; which method comprises treating said spen plating bath to induce random decomposition thereof, whereby the residue of said plating bath comprises a liquid having suspended therein a metallic precipitate containing about 88 to 94% nickel and 6 to 12% phosphorus by weight, separating said metallic precipitate from said liquid, and heating said separated metallic precipitate to a temperature sufciently high to melt the same, whereby the nickel and phosphorus constituents of said melt are alloyed upon subsequent cooling and solidifying thereof, said alloy being characterized by an eutectic composition comprising nickel and phosphorus constituents containing about 89% nickel and 11% phosphorous by weight and having an eutectic temperature of about 880 C.

2. The method set forth in claim l, wherein said spent chemical plating bath consists essentially of an aqueous solution of a nickel salt and an alkaline hypot phosphite.

3. The method set forth in claim 1, wherein said spent chemical plating bath is treated to induce said random decomposition thereof by seeding the same with previously produced metallic precipitate of the character specified.

4. The method set forth in claim 1, wherein said spen chemical plating bath is treated to induce said random decomposition thereof by seeding the same with previously made linely divided nickel-phosphorus alloy of the character specified.

5. The method of making a nickel-phosphorus alloy from a spent aqueous chemical plating bath containing nickel cations `and hypophosphite Aanions and phosphite anion; which method comprises treating said spent plating bath to induce random decomposition thereof, whereby the residue of `said plating bath comprises an -aqueous liquid having suspended therein a metallic precipitate, said metallic precipitate containing about 90 to 93% nickeland 7 to 10% phosphorus by weight and consisting essentially of an amorphous solid under-cooled solution of phosphorus in nickel, separating said metallic precipitate from said aqueous liquid, and heating said separated metallic precipitate to a temperature sufliciently high to melt the same, whereby the nickel and phosphorus constituents of said melt are alloyed upon subsequent cooling and solidifying thereof, said nickel-phosphorus alloy being characterized by the dispersion of nickel dendrites in the eutcctic composition thereof, said eutectic composition comprising nickel and phosphorus constituents containing about 89% nickel and 11% phosphorus by weight and having an eutectic temperature of about 880 C.

(References on following page) References Cited in the le of this patent UNITED STATES PATENTS -Fleitmann Mar. 3,0, 1880 Acker et a1. Mar. 2, 1937 Levy Mar. 23, 1937 Spowers et al. June 1, 1937 Huston et a1. lFeb. 14, 1939 Rapatz May 2, 1939 Lenz et al. May 23, 1939 Orr May 30, 1939 OTHER REFERENCES Hansen: Der Aufbau der Zweistofc gierun, gen, 1936, 10 Berlin, Springer, pages 936-937.

Claims

1. THE METHOD OF MAKING A NICKEL-PHOSPHORUS ALLOY FROM A "SPENT" CHEMICAL PLATING BATH CONTAINING NICKEL CATIONS AND HYPOPHOSPHITE ANIONS AND PHOSPHITE ANIONS; WHICH METHOD COMPRISES TRAEATING SAID "SPENT" PLATING BATH TO INDUCE "RANDOM DECOMPOSITION" THEREOF, WHEREBY THE RESIDUE OF SAID PLATING BATH COMPRISES A LIQUID HAVING SUSPENDED THEREIN A METALLIC PRECIPITATE CONTAINING ABOUT 88 TO 94% NICKEL AND 6 TO 12% PHOSPHORUS BY WEIGHT, SEPARATING SAID METALLIC PRECIPITATE FROM SAID LIQUID, AND HEATING SAID SEPARAARED METALLIC PRECIPITATE TO A TEMPERATURE SUFFICIENTLY HIGH TO MELT THE SAME, WHEREBY THE NICKEL AND PHOSPHORUS CONSTITUENTS OF SAID MELT ARE ALLOYED UPON SUBSEQUENT COOLING AND SOLIDIFYING THEREOF, SAID ALLOY BEING CHARACTERIZED BY AN EUTECTIC COMPOSITION COMPRISING NICKEL AND PHOSPHORUS CONSTITUENTS CONTAINING ABOUT 89% NICKEL AND 11% PHOSPHORUS BY WEIGHT AND HAVING AN EUTECTIC TEMPERATURE OF ABOUT 880* C.