US3185637A - Plating bath containing formaldehyde producing material - Google Patents
Plating bath containing formaldehyde producing material Download PDFInfo
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- US3185637A US3185637A US120207A US12020761A US3185637A US 3185637 A US3185637 A US 3185637A US 120207 A US120207 A US 120207A US 12020761 A US12020761 A US 12020761A US 3185637 A US3185637 A US 3185637A
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- formaldehyde
- bath
- reaction product
- zinc
- dicy
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- 238000007747 plating Methods 0.000 title claims description 26
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title description 100
- 239000000463 material Substances 0.000 title description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 37
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 35
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 20
- 229910052725 zinc Inorganic materials 0.000 claims description 20
- 239000011701 zinc Substances 0.000 claims description 20
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 13
- 239000004327 boric acid Substances 0.000 claims description 13
- 238000005282 brightening Methods 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 238000000151 deposition Methods 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 4
- 239000012895 dilution Substances 0.000 claims description 3
- 238000010790 dilution Methods 0.000 claims description 3
- 230000001376 precipitating effect Effects 0.000 claims description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 16
- 238000000576 coating method Methods 0.000 description 16
- 239000011248 coating agent Substances 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 12
- 229910000537 White brass Inorganic materials 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 11
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 229910001297 Zn alloy Inorganic materials 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 229910052759 nickel Inorganic materials 0.000 description 8
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 239000010941 cobalt Substances 0.000 description 6
- 229910017052 cobalt Inorganic materials 0.000 description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 6
- 235000019253 formic acid Nutrition 0.000 description 6
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 6
- 229960004889 salicylic acid Drugs 0.000 description 6
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 239000004312 hexamethylene tetramine Substances 0.000 description 4
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 4
- 229960004011 methenamine Drugs 0.000 description 4
- GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 4
- 229910000881 Cu alloy Inorganic materials 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- -1 chelates Chemical class 0.000 description 2
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- 229940044175 cobalt sulfate Drugs 0.000 description 1
- 229910000361 cobalt sulfate Inorganic materials 0.000 description 1
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- HZPNKQREYVVATQ-UHFFFAOYSA-L nickel(2+);diformate Chemical compound [Ni+2].[O-]C=O.[O-]C=O HZPNKQREYVVATQ-UHFFFAOYSA-L 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/22—Electroplating: Baths therefor from solutions of zinc
- C25D3/24—Electroplating: Baths therefor from solutions of zinc from cyanide baths
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/38—Electroplating: Baths therefor from solutions of copper
- C25D3/40—Electroplating: Baths therefor from solutions of copper from cyanide baths, e.g. with Cu+
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/56—Electroplating: Baths therefor from solutions of alloys
- C25D3/58—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of copper
Definitions
- This invention relates to the electrodeposition of copper, zinc and copper-zinc alloys and is particularly directed to an alkaline cyanide plating bath for depositing bright, mirror-like zinc and copper-zinc alloy deposits which contains a brightening agent as hereinafter described.
- the present invention provides an improved alkaline cyanide plating bath in which a polymer of a dicyandiamide and formaldehyde is used as a brightening agent.
- a suitable material for the brightening agent of the present invention is a polymer of formaldehyde and dicyandiamide.
- the polymer is preferably made by reacting dicyandiam-ide, formaldehyde and boric acid in a mole ratio of 1, 3.5-5, and 01-1 moles, respectively, at about 70 to 100 C. for about three to four hours.
- the resultant polymer is a resinous liquid, is soluble in both hot and cold water and is non-precipitating even on extreme dilution of the aqueous solution. Its aqueous solution is stable in water on standing and, generally, the more boric acid used in making the polymer, the more stable the solution.
- the final pH is around 7 /2 to 8 /2 in a 10% solution.
- Suitable brightening agents as effective as the dicy/ -formaldehyde/boric acid polymers, are condensation products of dicy, formaldehyde and formic acid. In these the reaction is not understood. They are produced by 3,185,537 Patented May 25, 1965 adding one mole dicy to 3 or more moles formic acid and then adding a mixture of 0.1 to 3 moles of formaldehyde to 1 to 4 moles of formic acid. The mixture is then refluxed at atmospheric pressure for several hours to several days and subsequently evacuated to a low pressure of the order of 20 mm. of mercury until the bulk of the formic acid has been evaporated out as determined by acidity tests. 4
- the product so formed has characteristics similar to those of the boric acid product but is also easier to control in a plating solution of alkaline zinc or zinc-copper alloy cyanide type.
- the bath As indicated above, generally about 0.005 to 2.5% by volume of the bath is generally the amount of brightening agent used.
- the 'brightener is the reaction product of dicyandiamide (sometimes called dicy), formaldehyde and boric acid. It is preferred that, for the best physical properties of the resultant coating such as density, fine grainness, low porosity, durability and brightness, a range of about ,4 to 2% by volume should be used although the best results are obtained with about 0.05 to 1.0 by volume of the bath. In any event, it has been found that when less than about 0.004% by volume of the brightener is used, there is little brightening effect and the coating is porous and of little commercial value. On the other hand, when more than 3.0% by volume of the polymer of dicy and formaldehyde is used, the resultant coating is irregular and becomes brittle an dark with increase of brightener.
- the resultant coating from the above described zinc cyanide bath is a bright ductile zinc deposit requiring no bright dip.
- the bath composition may be stabilized with a reaction product of salicylic acid and hexamethylene tetramine (sometimes called hexamine) using about /2 to 3 ounces per gal. of the above described reaction product.
- This reaction product generally contains a mixture of amino derivatives of salicylic acid.
- nickel and cobalt or mixtures thereof can be used in low free cyanide baths as such as those set forth in Table I.
- Nickel and cobalt may be added in the form of nickel or cobalt salts such as formates, carbonates, acetates, cyanides, chelates, or salts of nickel or cobalt and ethylene diamine or other poly amine in very small amounts, generally about 0.005 to 0.5 gram/liter to greatly increase the smoothness of the resultant coating.
- Nickel sulphate and cobalt sulfate usually are not dcsir+ able because they build up in the bath and a high level of sulfate is apparently harmful to the resultant coating.
- the nickel and cobalt increase smoothness and improve the plating in low current density areas by s! extending the plating range and the nickel by evening out the color. Likewise, nickel apparently increases the efficiency of plating in the low current density areas.
- Other metals which may be advantageously added as soluble salts, are copper and cadmium as well as traces of lead and thallium. However, these metals are not as effective as nickel or cobalt. In general, the use of nickel and cobalt increases corrosion resistance.
- Table II sets forth the preferred and general ranges of amounts of ingredients in a typical white brass or zinc-copper alloy plating bath: a
- the amount of reaction product of dicy and formaldehyde in a zinc alloy plating bath should be preferably as much as 0.05% by volume in order to get a dense, fine grained, low porosity and bright deposit.
- the above described bath is generally used at a current density of about 20-130 amperes per sq. ft.
- the operating temperatures of the bath generally range from 60 to 145 F. As is known in the art, in the temperature range between about 60 to 90 F. and above 124 F. the anodes are not polarized and thus, these temperatures are preferred for copper-zinc alloy cyanide plating baths.
- the copper-zinc alloy plated is more dense, finer grained, less porous, brightened and even leveled somewhat.
- white brass can be plated bright on metal surfaces such as steel and the like with no limitation on thickness. For instance, a layer 0.003 in. thick that takes 1 hour to plate can be just as bright as a layer plated in minutes.
- the white brass deposit Under a microscope, before the reaction product and dicy and formaldehyde is put in the bath the white brass deposit has numerous scattered pits or particles over the surface. The addition of the reaction product of dicy and formaldehyde reduces markedly and nearly eliminates this pitting or scattering of particles over the surface. After the reaction product is added, the resultant coating is more alloyed, evener and looks more fused.
- reaction product of idicy and formaldehyde permits the bright plating of sandwich layers of bright zinc and bright copperrich layers as well as white brass.
- reaction product of hexarnethylene tetramine and salicylic acid may be used in amounts of /3 to 3% by volume of bath (or about V2 to 4 02/ gal.) to stabilize the white brass bath illustrated in Table II'.
- Example 1 A zinc plating bath for the electrodeposition of zinc was prepared from the following ingredients.
- Zinc was plated from the above bath using a current density of 40 a.s.f. and a temperature of 88 F.
- the resultant plate was bright and ductile and had improved corrosion resistance.
- the smoothness and evenness was very good even in the low and high current density areas.
- Example 2 A white brass plating bath was made according to the formulation that follows.
- the resultant bath was heated to 82 F. and white brass plated therefrom for 60 minutes using a current density range of 60 a.s.f.
- the resultant plated coating was bright, dense, fine grained, and markedly low in porosity.
- Example 3 A white brass plating bath was made according to the formulation that follows.
- the resultant bath was heated to 82 F. and white brass r plated therefrom for 60 minutes using a current density range of 60 a.s.f.
- the resultant plated coating was bright, dense, fine grained, and low in porosity; the final coating being even smoother than the coating of Example 2 and slightly improved in the lower density areas.
- a coating plated from this formulation (except that no reaction product of dicy and formaldehyde was used) was not bright, poor in surface regularity and relatively brittle.
- Example 4 A bath was prepared using the same ingredients set forth in Example 2 except that a reaction product of hexarnine and salicylic acid was added in an amount of 2% by volume of the bath.
- the reaction product was produced by reaction of hexamine and salicylic acid at F. for 24 hours in an aqueous solution at a pH of 4.5 and the reaction mixture thereafter further reacted with potassium hydroxide to provide a pH of 9 /2.
- the above reaction product can be made by reacting about 1 to 4 moles of salicylic acid and 1 mole of hexamine at a temperature of about 125 to 190 F.
- the resultant bath was very stable, resulting in an economical bath.
- the resultant plated White brass coating was bright, dense, low in porosity and improved in corrosion resistance.
- reaction product of dicy and formaldehyde previously described may be substituted for the particular reaction product of dicy and formaldehyde used in the working examples to provide similar results.
- the use of the reaction product of 1 mole of dicy and 3.5 to 5 moles 'of formaldehyde, particularly with 0.1 to 1 mole of boric acid, as the brightening agent provides a denser deposit with an improvement in ductility as well as a reduced rate of corrosion.
- the polymer produced by reacting about 1 mole of dicy with about 0.1 to 3 moles of formaldehyde and about 4 to 10 moles of formic acid can be substituted for part or all of the reaction product of dicy and formaldehyde used in the working examples, to provide equivalent results.
- the sodium hydroxide used in the above examples can be substituted by another alkali metal hydroxide such as potassium hydroxide; likewise, in Examples 1 to 4, an alkali metal cyanide such as potassium cyanide can be substituted for all or part of the sodium cyanide to provide equivalent results.
- An aqueous plating bath of the alkaline cyanide type for depositing a metal comprising zinc the bath containing as a brightening agent about 0.005 to 2.5% by volume of a reaction product of about 1 mole of dicyandiamide, about 3.5 to 5 moles of formaldehyde, and about 0.1 to 1 mole of boric acid, the reaction products being soluble in cold water and non precipitating even on extreme dilution of aqueous solution, and the reaction product having a pH of about 7 /2 to 8 /2.
- An aqueous plating bath of the alkaline cyanide type for depositing a metal comprising zinc the bath containing about 0.005 to 3.0% by volume of a reaction product of (1) mixture of about 1 mole of dicyandiamide and about 3 to 6 moles of formaledhyde and (2) a mixture of about 0.1 to 3 moles of formaldehyde and about 1 to 4 moles of formic acid, the reaction product being soluble in alkaline solution.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Electroplating And Plating Baths Therefor (AREA)
Description
United States Patent ice 3,185,637 PLATING BATH CONTAG FORMALDEHYDE PRODUCING MATERIAL Anthony Debs, 13203 Canterbury Road, Cleveland, Ohio No Drawing. Filed June 28, 1961, Ser. No. 120,207 2 Claims. (Cl. 204-55) This invention relates to the electrodeposition of copper, zinc and copper-zinc alloys and is particularly directed to an alkaline cyanide plating bath for depositing bright, mirror-like zinc and copper-zinc alloy deposits which contains a brightening agent as hereinafter described.
It is an object of the present invention to provide an aqueous alkaline cyanide plating bath for the deposition of zinc or copper-zinc alloy coating, the coating being materially brighter in surface appearance than ordinary Zinc coatings and having good ductility and leveling.
It is an object of the present invention to provide an improved plating bath and a method of using the same for electrolytically depositing zinc, copper and copperzinc alloys, the bath containing a brightening agent comprising a reaction product of formaldehyde and di cyandiamide.
' It is an object of the present invention to provide a plating bath for the electrolytic deposition of zinc from a cyanide plating bath by use of a brightening agent comprising a reaction product of dicyandiamide and formaldehyde.
It is an object of the present invention to provide a method of electrodepositing a metal such as zinc or a zinc copper-alloy from a plating bath in which a polymer of formaldehyde and dicyandiamide is used as a brightening agent.
It is an object of the present invention to provide a white brass or copper-Zinc alloy cyanide plating bath in which a polymer of'dicyandiamide and formaldehyde is used as the brightening agent.
The present invention provides an improved alkaline cyanide plating bath in which a polymer of a dicyandiamide and formaldehyde is used as a brightening agent.
A suitable material for the brightening agent of the present invention is a polymer of formaldehyde and dicyandiamide. The polymer is preferably made by reacting dicyandiam-ide, formaldehyde and boric acid in a mole ratio of 1, 3.5-5, and 01-1 moles, respectively, at about 70 to 100 C. for about three to four hours. The resultant polymer is a resinous liquid, is soluble in both hot and cold water and is non-precipitating even on extreme dilution of the aqueous solution. Its aqueous solution is stable in water on standing and, generally, the more boric acid used in making the polymer, the more stable the solution.
As pointed out in the US. Patent No. 2,852,490, which describes the preparation of a suitable dicy/formaldehyde/'boric acid polymer; the pH of the reaction solution generally should be initially below 7; the pH remains below 7 at first and, then, upon reaction of the ingredients, the pH of the solution rises and becomes practically constant.
While the polymer of dicyandiamide, formaldehyde and boric acid can be made with 1 to 5 moles of formaldehyde per mole of dicyandiamide, it has been found that only a 3.5 to 5 mole range gives solutions which are clear in cold water and stable. Upon standing, solutions of the polymers develop haziness and insolubility in cold water when only three moles of formaldehyde are used.
Continuing to describe the reaction, generally, the final pH is around 7 /2 to 8 /2 in a 10% solution.
Other suitable brightening agents, as effective as the dicy/ -formaldehyde/boric acid polymers, are condensation products of dicy, formaldehyde and formic acid. In these the reaction is not understood. They are produced by 3,185,537 Patented May 25, 1965 adding one mole dicy to 3 or more moles formic acid and then adding a mixture of 0.1 to 3 moles of formaldehyde to 1 to 4 moles of formic acid. The mixture is then refluxed at atmospheric pressure for several hours to several days and subsequently evacuated to a low pressure of the order of 20 mm. of mercury until the bulk of the formic acid has been evaporated out as determined by acidity tests. 4
To this mixture is then added cold very concentrated alkali hydroxide solution and the evaporation is continued until the solution becomes alkaline andbubbling and frothing cease. The product so formed has characteristics similar to those of the boric acid product but is also easier to control in a plating solution of alkaline zinc or zinc-copper alloy cyanide type.
A typical :bath for plating zinoin accordance with the present invention is given below in Table I, the table setting forth both the general ranges and the preferred ranges of each of the ingredients:
2 Percent by volume determined by trial in Hull cell.
As indicated above, generally about 0.005 to 2.5% by volume of the bath is generally the amount of brightening agent used. The 'brightener is the reaction product of dicyandiamide (sometimes called dicy), formaldehyde and boric acid. It is preferred that, for the best physical properties of the resultant coating such as density, fine grainness, low porosity, durability and brightness, a range of about ,4 to 2% by volume should be used although the best results are obtained with about 0.05 to 1.0 by volume of the bath. In any event, it has been found that when less than about 0.004% by volume of the brightener is used, there is little brightening effect and the coating is porous and of little commercial value. On the other hand, when more than 3.0% by volume of the polymer of dicy and formaldehyde is used, the resultant coating is irregular and becomes brittle an dark with increase of brightener.
The resultant coating from the above described zinc cyanide bath is a bright ductile zinc deposit requiring no bright dip.
If desired, the bath composition may be stabilized with a reaction product of salicylic acid and hexamethylene tetramine (sometimes called hexamine) using about /2 to 3 ounces per gal. of the above described reaction product. This reaction product generally contains a mixture of amino derivatives of salicylic acid.
Also in accordance with another aspect of the present invention, nickel and cobalt or mixtures thereof can be used in low free cyanide baths as such as those set forth in Table I. Nickel and cobalt may be added in the form of nickel or cobalt salts such as formates, carbonates, acetates, cyanides, chelates, or salts of nickel or cobalt and ethylene diamine or other poly amine in very small amounts, generally about 0.005 to 0.5 gram/liter to greatly increase the smoothness of the resultant coating. Nickel sulphate and cobalt sulfate usually are not dcsir+ able because they build up in the bath and a high level of sulfate is apparently harmful to the resultant coating. In any event, the nickel and cobalt increase smoothness and improve the plating in low current density areas by s! extending the plating range and the nickel by evening out the color. Likewise, nickel apparently increases the efficiency of plating in the low current density areas. Other metals, which may be advantageously added as soluble salts, are copper and cadmium as well as traces of lead and thallium. However, these metals are not as effective as nickel or cobalt. In general, the use of nickel and cobalt increases corrosion resistance.
Returning to the advantage of using the bath of Table I, upon the addition of the reaction product of dicy and formaldehyde (which preferably has an average molecular weight range of about 2000 to 8000 or 10,000) the deposited metal evens out and brightens up the normally poor deposits in high current density areas. This is one of the main advantages of adding the reaction product of dicy and formaldehydethe improvement of deposits in high current density areas and making the deposits bright, even and dense.
In a manner similar to Table I, Table II below sets forth the preferred and general ranges of amounts of ingredients in a typical white brass or zinc-copper alloy plating bath: a
1 Percent by volume of bath. 2 Percent determined by trial.
As indicated above, the amount of reaction product of dicy and formaldehyde in a zinc alloy plating bath should be preferably as much as 0.05% by volume in order to get a dense, fine grained, low porosity and bright deposit.
The above described bath is generally used at a current density of about 20-130 amperes per sq. ft. The operating temperatures of the bath generally range from 60 to 145 F. As is known in the art, in the temperature range between about 60 to 90 F. and above 124 F. the anodes are not polarized and thus, these temperatures are preferred for copper-zinc alloy cyanide plating baths.
In the presence of the reaction product of dicy and formaldehyde, the copper-zinc alloy plated is more dense, finer grained, less porous, brightened and even leveled somewhat. Using the reaction product of dicy and formaldehyde in the bath of Table II, white brass can be plated bright on metal surfaces such as steel and the like with no limitation on thickness. For instance, a layer 0.003 in. thick that takes 1 hour to plate can be just as bright as a layer plated in minutes. Under a microscope, before the reaction product and dicy and formaldehyde is put in the bath the white brass deposit has numerous scattered pits or particles over the surface. The addition of the reaction product of dicy and formaldehyde reduces markedly and nearly eliminates this pitting or scattering of particles over the surface. After the reaction product is added, the resultant coating is more alloyed, evener and looks more fused.
Another feature of the use of 'the reaction product of idicy and formaldehyde is that it permits the bright plating of sandwich layers of bright zinc and bright copperrich layers as well as white brass. Also, as discussed in the case of the zinc bathof Table I, in a similar manner, the reaction product of hexarnethylene tetramine and salicylic acid may be used in amounts of /3 to 3% by volume of bath (or about V2 to 4 02/ gal.) to stabilize the white brass bath illustrated in Table II'.
In general, as the amount of reaction product of dicy and formaldehyde is increased in the brass bath of Table II, the low density areas tend to be copper-rich instead of zinc-rich.
The following examples are intended to illustrate the present invention and not to limit it in any way.
Example 1 A zinc plating bath for the electrodeposition of zinc was prepared from the following ingredients.
Ingredients: Oz. per gal. Zinc cyanide 8 Sodium hydroxide 10 Sodium cyanide 4 Reaction product of dicy, formaldehyde and boric acid .01
Zinc was plated from the above bath using a current density of 40 a.s.f. and a temperature of 88 F. The resultant plate was bright and ductile and had improved corrosion resistance. The smoothness and evenness was very good even in the low and high current density areas.
Example 2 A white brass plating bath was made according to the formulation that follows.
Ingredients: Oz. per gal. Zinc cyanide 5 Copper cyanide 2.4 Sodium cyanide 7.8 Sodium hydroxide 4.5 Reaction product of dicy, formaldehyde and boric acid 1 0.1
1 Percent by volume of the bath or about 0.15 oz./per gal.
The resultant bath was heated to 82 F. and white brass plated therefrom for 60 minutes using a current density range of 60 a.s.f. The resultant plated coating was bright, dense, fine grained, and markedly low in porosity.
Example 3 A white brass plating bath was made according to the formulation that follows.
Ingredients: Oz. per gal. Zinc cyanide 5 Copper cyanide 2.4 Sodium cyanide 7.8 Sodium hydroxide -i 4.5
Reaction product of dicy, formaldehyde and boric acid 1 0.1 Nickel formate 0.05
1 Percent by volume of the bath or about 0.15 oz./per gal.
50 The resultant bath was heated to 82 F. and white brass r plated therefrom for 60 minutes using a current density range of 60 a.s.f. The resultant plated coating was bright, dense, fine grained, and low in porosity; the final coating being even smoother than the coating of Example 2 and slightly improved in the lower density areas. In contrast to this, a coating plated from this formulation (except that no reaction product of dicy and formaldehyde was used) was not bright, poor in surface regularity and relatively brittle.
Example 4 A bath was prepared using the same ingredients set forth in Example 2 except that a reaction product of hexarnine and salicylic acid was added in an amount of 2% by volume of the bath. The reaction product was produced by reaction of hexamine and salicylic acid at F. for 24 hours in an aqueous solution at a pH of 4.5 and the reaction mixture thereafter further reacted with potassium hydroxide to provide a pH of 9 /2. In general, the above reaction product can be made by reacting about 1 to 4 moles of salicylic acid and 1 mole of hexamine at a temperature of about 125 to 190 F. and a pH of about 2 /2 to 5 /2 for at least 4 hours and thereafter reacting the reaction mixture with about 2 to 4 moles of an alkali hydroxide to provide the final reaction product having a pH of about 8 to 12 and preferably about 9% to 10 /2.
The resultant bath was very stable, resulting in an economical bath. The resultant plated White brass coating was bright, dense, low in porosity and improved in corrosion resistance.
In the above examples, other suitable reaction products of dicy and formaldehyde previously described may be substituted for the particular reaction product of dicy and formaldehyde used in the working examples to provide similar results. In all the zinc and zinc-alloy plating baths, such as illustrated in the examples, the use of the reaction product of 1 mole of dicy and 3.5 to 5 moles 'of formaldehyde, particularly with 0.1 to 1 mole of boric acid, as the brightening agent, provides a denser deposit with an improvement in ductility as well as a reduced rate of corrosion. As an equally useful alternative as previously indicated, the polymer produced by reacting about 1 mole of dicy with about 0.1 to 3 moles of formaldehyde and about 4 to 10 moles of formic acid can be substituted for part or all of the reaction product of dicy and formaldehyde used in the working examples, to provide equivalent results.
In a similar manner, the sodium hydroxide used in the above examples can be substituted by another alkali metal hydroxide such as potassium hydroxide; likewise, in Examples 1 to 4, an alkali metal cyanide such as potassium cyanide can be substituted for all or part of the sodium cyanide to provide equivalent results.
What is claimed is:
1. An aqueous plating bath of the alkaline cyanide type for depositing a metal comprising zinc, the bath containing as a brightening agent about 0.005 to 2.5% by volume of a reaction product of about 1 mole of dicyandiamide, about 3.5 to 5 moles of formaldehyde, and about 0.1 to 1 mole of boric acid, the reaction products being soluble in cold water and non precipitating even on extreme dilution of aqueous solution, and the reaction product having a pH of about 7 /2 to 8 /2.
2. An aqueous plating bath of the alkaline cyanide type for depositing a metal comprising zinc, the bath containing about 0.005 to 3.0% by volume of a reaction product of (1) mixture of about 1 mole of dicyandiamide and about 3 to 6 moles of formaledhyde and (2) a mixture of about 0.1 to 3 moles of formaldehyde and about 1 to 4 moles of formic acid, the reaction product being soluble in alkaline solution.
References Cited by the Examiner UNITED STATES PATENTS 2,411,397 11/46 Walker. 2,451,426 10/48 Bair et al. 2,621,152 12/52 Hoifman. 2,852,490 9/58 Sellet et al. 260- FOREIGN PATENTS 461,074 11/49 Canada.
JOHN H. MACK, Primary Examiner.
JOHN R. SPECK, MURRAY TILLMAN, Examiners.
Claims (1)
1. AN AQUEOUS PLATING BATH OF THE ALKALINE CYANIDE TYPE FOR DEPOSITING A METAL COMPRISING ZINC, THE BATH CONTAINING AS A BRIGHTENING AGENT ABOUT 0.005 TO 2.5% BY VOLUME OF A REACTION PRODUCT OF ABOUT 1 MOLE OF DICYANDIAMIDE, ABOUT 3.5 TO 5 MOLES OF FORMALDEHYDE, AND ABOUT 0.1 TO 1 MOLE OF BORIC ACID, THE REACTION PRODUCTS BEING SOLUBLE IN COLD WATER AND NON PRECIPITATING EVEN ON EXTREME DILUTION OF AQUEOUS SOLUTION, AND THE REACTION PRODUCT HAVING A PH OF ABOUT 7 1/2 TO 8 1/2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US120207A US3185637A (en) | 1961-06-28 | 1961-06-28 | Plating bath containing formaldehyde producing material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US120207A US3185637A (en) | 1961-06-28 | 1961-06-28 | Plating bath containing formaldehyde producing material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3185637A true US3185637A (en) | 1965-05-25 |
Family
ID=22388886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US120207A Expired - Lifetime US3185637A (en) | 1961-06-28 | 1961-06-28 | Plating bath containing formaldehyde producing material |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3185637A (en) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2411397A (en) * | 1945-07-04 | 1946-11-19 | Du Pont | Production of sodium cyanamideformaldehyde condensation product |
| US2451426A (en) * | 1943-11-25 | 1948-10-12 | Du Pont | Bright zinc plating |
| CA461074A (en) * | 1949-11-15 | Richard Bair Robert | Bright zinc plating | |
| US2621152A (en) * | 1950-03-30 | 1952-12-09 | Allied Res Products Inc | Zinc cyanide plating bath |
| US2852490A (en) * | 1954-07-21 | 1958-09-16 | Jacques Wolf & Co | Dicyandiamide, formaldehyde and boric acid condensation product |
-
1961
- 1961-06-28 US US120207A patent/US3185637A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA461074A (en) * | 1949-11-15 | Richard Bair Robert | Bright zinc plating | |
| US2451426A (en) * | 1943-11-25 | 1948-10-12 | Du Pont | Bright zinc plating |
| US2411397A (en) * | 1945-07-04 | 1946-11-19 | Du Pont | Production of sodium cyanamideformaldehyde condensation product |
| US2621152A (en) * | 1950-03-30 | 1952-12-09 | Allied Res Products Inc | Zinc cyanide plating bath |
| US2852490A (en) * | 1954-07-21 | 1958-09-16 | Jacques Wolf & Co | Dicyandiamide, formaldehyde and boric acid condensation product |
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