US3309293A - Copper cyanide electroplating bath - Google Patents
Copper cyanide electroplating bath Download PDFInfo
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- US3309293A US3309293A US411543A US41154364A US3309293A US 3309293 A US3309293 A US 3309293A US 411543 A US411543 A US 411543A US 41154364 A US41154364 A US 41154364A US 3309293 A US3309293 A US 3309293A
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- bath
- cyanide
- copper
- baths
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- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 title description 13
- 238000009713 electroplating Methods 0.000 title description 3
- LEKPFOXEZRZPGW-UHFFFAOYSA-N copper;dicyanide Chemical compound [Cu+2].N#[C-].N#[C-] LEKPFOXEZRZPGW-UHFFFAOYSA-N 0.000 claims description 15
- 238000007747 plating Methods 0.000 claims description 12
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000654 additive Substances 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 239000000080 wetting agent Substances 0.000 description 7
- -1 cationic quaternary ammonium chloride compounds Chemical class 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- PSBDWGZCVUAZQS-UHFFFAOYSA-N (dimethylsulfonio)acetate Chemical group C[S+](C)CC([O-])=O PSBDWGZCVUAZQS-UHFFFAOYSA-N 0.000 description 4
- FEWJPZIEWOKRBE-JCYAYHJZSA-L L-tartrate(2-) Chemical compound [O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-L 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 4
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical class [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 4
- 239000011669 selenium Substances 0.000 description 4
- 235000011006 sodium potassium tartrate Nutrition 0.000 description 4
- 229940117986 sulfobetaine Drugs 0.000 description 4
- 229940095064 tartrate Drugs 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 238000005282 brightening Methods 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 239000003752 hydrotrope Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- IZWSFJTYBVKZNK-UHFFFAOYSA-N lauryl sulfobetaine Chemical compound CCCCCCCCCCCC[N+](C)(C)CCCS([O-])(=O)=O IZWSFJTYBVKZNK-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 229910052716 thallium Inorganic materials 0.000 description 2
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 2
- DKZRLCHWDNEKRH-UHFFFAOYSA-N 1-nonoxynonane Chemical compound CCCCCCCCCOCCCCCCCCC DKZRLCHWDNEKRH-UHFFFAOYSA-N 0.000 description 1
- ORTUYCUWCKNIND-UHFFFAOYSA-N 3-[2-(2-aminoethylamino)ethylamino]propanenitrile Chemical compound NCCNCCNCCC#N ORTUYCUWCKNIND-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- SLEGPTUZZMEOPB-UHFFFAOYSA-N [Na].C(CCCCCCCCC)N Chemical compound [Na].C(CCCCCCCCC)N SLEGPTUZZMEOPB-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical compound OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- FMJJKGCANRBYNT-UHFFFAOYSA-L dipotassium dioxido(selanylidene)-lambda4-sulfane Chemical compound S(=[Se])([O-])[O-].[K+].[K+] FMJJKGCANRBYNT-UHFFFAOYSA-L 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940085675 polyethylene glycol 800 Drugs 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- IYKVLICPFCEZOF-UHFFFAOYSA-N selenourea Chemical compound NC(N)=[Se] IYKVLICPFCEZOF-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- HSFQBFMEWSTNOW-UHFFFAOYSA-N sodium;carbanide Chemical group [CH3-].[Na+] HSFQBFMEWSTNOW-UHFFFAOYSA-N 0.000 description 1
- AGGIJOLULBJGTQ-UHFFFAOYSA-N sulfoacetic acid Chemical compound OC(=O)CS(O)(=O)=O AGGIJOLULBJGTQ-UHFFFAOYSA-N 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-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
- C25D3/38—Electroplating: Baths therefor from solutions of copper
- C25D3/40—Electroplating: Baths therefor from solutions of copper from cyanide baths, e.g. with Cu+
Definitions
- the present invention is directed to electroplating, more particularly to an improvement in a copper cyanide plating bath whereby higher efficiency is obtained.
- the concentration of betaine to be effective was comparatively high, the minimum being .075 gram per liter.
- the tolerance thereof to organic compounds was low, and the rinsability of the coating was far from that desired. Also, the brightening effect was only moderate.
- the present invention is intended to overcome the deficiencies of the prior art, it being among the objects thereof to provide an additive to a cyanide copper plating bath which will not only impart improved brightness thereto, but will also be effective in the low current density areas.
- R is CH (CH and the CH chain may have some unsaturated radicals, having y carbon atoms, and y is to 25.
- R and R are the same or different radicals taken from the class of H and-alkyl and hydroxy alkyl having 1 to 4 carbon atoms,-n is 1 to 6.
- the components include the anhydrides wherein S is linked to N through oxygen. Examples of such radicals are oleyl, myristyl, methyl, octyl, hydroxy propyl, and the like.
- Such components are very active surface active wetting agents when used alone. They also improve the characteristics of other known wetting agents, including those described below.
- the sulfobetaines show synergistic effects. For instance, many such adducts exhibit reduced solubility in the bath and cause cloudiness at increased temperatures. Such cloudiness is greatly reduced and even completely eliminated when the sulfobetaines are added to the bath.
- metallic addition agents are used to help brighten the deposit.
- Some of the metallics which have been proposed are the soluble salts of lead, antimony, bismuth, thallium and arsenic.
- Lead, antimony and thallium have been used in conjunction with sulfur compounds such as thiocyanate or with selenium compounds. They, however, have the undesirable characteristic of occasionally causing rough deposits.
- sulfur compounds such as thiocyanate or with selenium compounds. They, however, have the undesirable characteristic of occasionally causing rough deposits.
- the plating bath was idle, they tended to deposit on the anode by immersion and were thus removed from solution. This deposition necessitated the use of excessively large amounts of these metallics and required a period of initial electrolysis to dissolve the deposited metallic bright-- eners from the anodes in order to make them effective in the bath.
- the aforementioned addition agents are compounds having the following formulas wherein n is 2 to R is aryl or alkyl containing from 6 to 20 carbon atoms. R is (CH COOH where y is 1 to 6.
- nitrogen containing compounds are preferred to the others, although a beneficial effect upon the bath is produced by the use of any one or more.
- ampholytic compounds those compounds which have the property of dissociation in either acid or basic media.
- R is aryl or alkyl containing from 6 to 20 carbon atoms.
- R is (CH .SO H, wherein y is 1 to 6.
- modified ethylene oxide compound 7 it is also possible using the modified ethylene oxide compound 7 to provide additives which do not readily cloud when used in high concentrations in the bath without impairing the beneficial effect thereof on the heavy metal addition agents.
- modified compounds have an improved cloud point, impart brightness to the cyanide copper baths and still maintain the desirable property of reacting with heavy metal addition agents.
- ethylene oxide-carboxy acid ampholytes of Example 7 and the sulfonic ampholytes of Example 8 are also effective brighteners in the cyanide copper baths and are completely stable under all normal conditions of operation.
- the present invention overcomes practically all of the defects above noted. Applicants have obtained superior brightening of the deposits and particularly so in the low current density areas. They obtain better rinsability of the work, and have eliminated the tendency to water breaking.
- the additives produce greater tolerance to the presence of contaminants of organic nature. When used in conjunction with other wetting agents they act as improved hydrotropes.
- Our baths are notably effective to give excellent results in low free cyanide baths. The baths are not subject to skip plating.
- Example 6 CuCN 60 KCN 95 KOH 30 KCNS 15 Sb as tartrate .008 Lau'ryl thioether of polypropylene glycol 1000 .05 Lauryl amine sulfoacetate 0.4
- y is 1 to 6
- R is a radical selected from the group consisting of aliphatic chains having 6 to 20 carbon atoms
- R and R are radicals selected from the group consisting of alkyl having 1 to 4 carbon atoms; the amount of said additive being from 0.001 g/l. to the limit of solubility.
- An alkaline cyanide copper bath according to claim 2 characterized in that it contains polyglycol ethers hav- 6 ing surface activity, said ethers having 2 to 100 ethoxy groups.
- An alkaline cyanide copper bath according to claim 1 characterized in that there is also present an agent which is selected from the group consisting of an ethoxylated alcohol amine and thio-alcohol.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electroplating And Plating Baths Therefor (AREA)
Description
3,309,293 COPPER CYANIDE ELECTROPLATING BATH Barnet D. Ostrow and Fred 1. Nobel, Roslyn, N.Y., assignors to Elechem Corp., Jersey City, N.J., a corporation of New Jersey N Drawing. Filed Nov. 16, 1964, Ser. No. 411,543
4 Claims. (Cl. 204-52) This application is a continuation-in-part of co-pending application Ser. No. 636,862 filed Jan. 29, 1957, now abandoned, for Copper Bath With Alkylene Oxide Derivatives, which is a continuation-in-part of Ser. No.
78,908 filed Dec. 30, 1954, now abandoned, for Copper Plating Composition.
The present invention is directed to electroplating, more particularly to an improvement in a copper cyanide plating bath whereby higher efficiency is obtained.-
The addition of surface active agents to cyanide copper baths has been proposed frequently in the past to increase the tolerance of the baths toward organic addition agents and these agents were required to be present in cornpara tively large concentrations. For example, the use of alkyl betaines has been sugggested. In order to overcome the adverse effects of water breaks inherent in thesematerials, cationic quaternary ammonium chloride compounds were incorporated therewith.
The concentration of betaine to be effective was comparatively high, the minimum being .075 gram per liter. The tolerance thereof to organic compounds was low, and the rinsability of the coating was far from that desired. Also, the brightening effect was only moderate.
The present invention is intended to overcome the deficiencies of the prior art, it being among the objects thereof to provide an additive to a cyanide copper plating bath which will not only impart improved brightness thereto, but will also be effective in the low current density areas.
It is also among the objects of the invention to introduce such an additive which will give better rinsability with little or no tendency for water breaking, have greater tolerance to organic contamination, and be compatible with other bath additives.
It is further among the objects to provide a substance which will act as an improved hydrotrope when used in conjunction with other wetting agents and will show synergistic effects.
In practicing the invention, there is added to the bath a compound of the following general formula, that is a sulfobetaine:
wherein R is CH (CH and the CH chain may have some unsaturated radicals, having y carbon atoms, and y is to 25. R and R are the same or different radicals taken from the class of H and-alkyl and hydroxy alkyl having 1 to 4 carbon atoms,-n is 1 to 6.- The components include the anhydrides wherein S is linked to N through oxygen. Examples of such radicals are oleyl, myristyl, methyl, octyl, hydroxy propyl, and the like.
Such components are very active surface active wetting agents when used alone. They also improve the characteristics of other known wetting agents, including those described below.
In conjunction with such brightening agents, such as the ethylene oxide adducts, the sulfobetaines show synergistic effects. For instance, many such adducts exhibit reduced solubility in the bath and cause cloudiness at increased temperatures. Such cloudiness is greatly reduced and even completely eliminated when the sulfobetaines are added to the bath.
States Patent 0 Cyanide copper plating baths, particularly the high efliciency baths, operating with a low free cyanide content, are desirable for improved and broader bright current density range and higher efficiency. However, such baths are highly sensitive to skip plating and they exhibit dullness in the low current density range when contaminated with organic substances. The prior carboxy betaines and carboxy acids do not improve the brightness in the low current density areas to any such extent as the sulfobetaines under equivalent conditions.
In cyanide copper plating, numerous metallic addition agents are used to help brighten the deposit. Some of the metallics which have been proposed are the soluble salts of lead, antimony, bismuth, thallium and arsenic. Lead, antimony and thallium have been used in conjunction with sulfur compounds such as thiocyanate or with selenium compounds. They, however, have the undesirable characteristic of occasionally causing rough deposits. Also, when the plating bath was idle, they tended to deposit on the anode by immersion and were thus removed from solution. This deposition necessitated the use of excessively large amounts of these metallics and required a period of initial electrolysis to dissolve the deposited metallic bright-- eners from the anodes in order to make them effective in the bath.
It has been found that certain surface active wetting agents when used in cyanide copper electrolytes in conjunction with certain metallic addition agents, prevent the metallics from depositing on the copper anode by immersion when the bath is idle. They thus reduce the necessity of requiring higher concentrations of these metallics .in order to be eifective and hence reduce or eliminate the tendency to cause roughness of the deposit. These wetting agents are also beneficial when used alone or in combination with each other as herein subsequently described.
The aforementioned addition agents are compounds having the following formulas wherein n is 2 to R is aryl or alkyl containing from 6 to 20 carbon atoms. R is (CH COOH where y is 1 to 6.
Of these agents, nitrogen containing compounds are preferred to the others, although a beneficial effect upon the bath is produced by the use of any one or more.
Many of the aforementioned compounds can be used in small concentrations, for example .001 to .01 gram per liter, and still remain effective. It is true, however, that under certain conditions higher concentrations may be required or desired and are not harmful. These concentrations may go up to the limit of solubility of the particular compound used. Since these materials have the characteristic of increasing the tolerance of the cyanide copper bath to organic contamination, they may also be used in higher concentrations to overcome the effect of organic contamination in addition to having the beneficial effect referred to above on the heavy metals. However, with very high concentrations, many of these ethylene oxide condensates tend to cloud or even salt out under the operating conditions of the cyanide copper baths and thus tend to limit the concentration which can effectively remain in solution.
It has been found that by incorporating with these ethylene oxide compounds small amounts of ampholytic surface active agents or anionic wetting agents, a reduction in the clouding tendency is obtained, permitting the use of larger amounts of these condensates. By ampholytic compounds is meant those compounds which have the property of dissociation in either acid or basic media. The ampholytic compounds which have been found satisfactory for the use described in the foregoing paragraphs are as follows:
8 RNHR R is aryl or alkyl containing from 6 to 20 carbon atoms. R is (CH .SO H, wherein y is 1 to 6.
It is also possible using the modified ethylene oxide compound 7 to provide additives which do not readily cloud when used in high concentrations in the bath without impairing the beneficial effect thereof on the heavy metal addition agents.
These modified compounds have an improved cloud point, impart brightness to the cyanide copper baths and still maintain the desirable property of reacting with heavy metal addition agents. These ethylene oxide-carboxy acid ampholytes of Example 7 and the sulfonic ampholytes of Example 8 are also effective brighteners in the cyanide copper baths and are completely stable under all normal conditions of operation.
In view of the disadvantages inherent in prior art additives, the present invention overcomes practically all of the defects above noted. Applicants have obtained superior brightening of the deposits and particularly so in the low current density areas. They obtain better rinsability of the work, and have eliminated the tendency to water breaking. The additives produce greater tolerance to the presence of contaminants of organic nature. When used in conjunction with other wetting agents they act as improved hydrotropes. Our baths are notably effective to give excellent results in low free cyanide baths. The baths are not subject to skip plating.
The following examples will serve to further illustrate this invention, the conditions of operation being the same as for the standard cyanide copper bath, the amounts being grams per liter (g./l.). The conditions of operation are those ordinarily used in Hull cell operation. A temperature of about 140 to 180 F. is used with a current density of about 10 to 60 amperes per square foot. Plating is conducted for 10 minutes with continuous agitation:
Example 1 CuCN 6O KCN 90 KOH 3O Rochelle salts 45 T1 as a soluble salt .007 Se as K Se .004 Lauryl amine of polyethylene glycol 660 .02 Sodium ethyl taurate of lauryl amine .08
Example 2 CuCN 60.0 KCN 95.0 KOH 30.0 Rochelle salts 25.0 C H OPO (C H O) H 0.15 Se as K SeO 0.3 Lauryl sulfobetaine 0.2
Example 3 CuCN 45.0 KCN 83.0 KOH 30.0
Decylamine sodium ethyltaurate 0.25
Sodium acetate of lauryl amine polyethylene glycol 660 (C H N(C H O) H)CH.COONa 0.25
Example 5 CuCN 60 KCN KOH 30 KCNS 15 Sb as tartrate 008 Lauryl diethylenetriamine of polyethylene glycol 800 0.1
Lauryl dimethyl sulfobetaine 0.5
Example 6 CuCN 60 KCN 95 KOH 30 KCNS 15 Sb as tartrate .008 Lau'ryl thioether of polypropylene glycol 1000 .05 Lauryl amine sulfoacetate 0.4
Example 7 Copper cyanide 60.0 Free KCN 12.0
KOH 45.0
NaCNS 15.0
KSb Tartrate 0.02
Cetyldimethyl sulfobetaine 0.3
Example 8 Copper Cyanide 45.0 Free KCN 10.0
K Tartrate 45.0
Selenourea .003
Pb acetate .004 Nonyl ether of polyethylene glycol 2000 0.20 O'leyldimethyl sulfo betaine 0.1
Example 9 CuCN 60 KCN 95 KOH 25 Rochelle salts 30 Se as selenourela .003 Methyl, hydroxyethyl, cetyl su'lfob'etaine 1.0
Example 10 CuCN 45 KCN 70 KOH 15 Rochelle salts 30 Se as potassium selenosulfite .005 Sodium methyl taurateof decylamine 0.2
Example 11 CuCN 60 KCN KOH 30 Potassium citrate 30 Dimethyl, lauryl sulfobetaine .03
While only a certain number of specific embodiments of this invention have been described, nevertheless this invention is not limited thereto and such changes as may be apparent to one skilled in the art may be made Without departing from the spirit thereof. Furthermore, this specification is to be broadly construed and not to be limited except by the character of the claims appended hereto.
In the claims there are listed a number of sulfonic acids. These may be introduced or used in the form of the soluble salts thereof. Such salts are formed in the alkaline baths when the free acids are added.
What is claimed is:
1. In an aqueous alkaline cyanide copper plating bath, the improvement which comprises the addition to said bath of RNH(OH SO X; in the amount of 0.001 g/l. to the limit of solubility and wherein R is a radical selected from the group consisting of alkyl radicals having 6 to 20 carbon atoms, X is H or alkali metal, and y is 1 to 6.
2. In an aqueous alkaline cyanide copper plating bath, the improvement which comprises the addition to said bath of at least one compound selected from the group consisting of wherein y is 1 to 6; R is a radical selected from the group consisting of aliphatic chains having 6 to 20 carbon atoms; and R and R are radicals selected from the group consisting of alkyl having 1 to 4 carbon atoms; the amount of said additive being from 0.001 g/l. to the limit of solubility.
3. An alkaline cyanide copper bath according to claim 2, characterized in that it contains polyglycol ethers hav- 6 ing surface activity, said ethers having 2 to 100 ethoxy groups.
4. An alkaline cyanide copper bath according to claim 1, characterized in that there is also present an agent which is selected from the group consisting of an ethoxylated alcohol amine and thio-alcohol.
References Cited by the Examiner UNITED STATES PATENTS 20 JOHN H. MACK, Primary Examiner.
ALLEN B. CURTIS, Examiner.
G. KAPLAN, Assistant Examiner.
Claims (1)
1. IN AN AQUEOUS ALKALINE CYANIDE COPPER PLATING BATH, THE IMPROVEMENT WHICH COMPRISES THE ADDITION TO SAID BATH OF RNH(CH2)YSO3X; IN THE AMOUNT OF 0.001 G/L. TO THE LIMIT OF SOLUBILITY AND WHEREIN R IS A RADICAL SELECTED FROM THE GROUP CONSISTING OF ALKYL RADICALS HAVING 6 TO 20 CARBON ATOMS, X IS H OR ALKALI METAL, AND Y IS 1 TO 6.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US411543A US3309293A (en) | 1964-11-16 | 1964-11-16 | Copper cyanide electroplating bath |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US411543A US3309293A (en) | 1964-11-16 | 1964-11-16 | Copper cyanide electroplating bath |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3309293A true US3309293A (en) | 1967-03-14 |
Family
ID=23629365
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US411543A Expired - Lifetime US3309293A (en) | 1964-11-16 | 1964-11-16 | Copper cyanide electroplating bath |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3309293A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4376685A (en) * | 1981-06-24 | 1983-03-15 | M&T Chemicals Inc. | Acid copper electroplating baths containing brightening and leveling additives |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2255057A (en) * | 1939-10-02 | 1941-09-09 | Du Pont | Electroplating copper |
| US2541700A (en) * | 1946-02-28 | 1951-02-13 | Du Pont | Electroplating copper |
| US2765269A (en) * | 1954-11-19 | 1956-10-02 | Barnet D Ostrow | Bath for plating bright gold |
| US2817627A (en) * | 1955-07-11 | 1957-12-24 | Barnet D Ostrow | Process for plating bright brass |
| US2828252A (en) * | 1953-04-28 | 1958-03-25 | Degussa | Electrodeposition of bright zinc, copper, or nickel |
| US2848394A (en) * | 1956-05-04 | 1958-08-19 | Hanson Van Winkle Munning Co | Bright copper plating |
| US2873234A (en) * | 1957-06-19 | 1959-02-10 | Metal & Thermit Corp | Electrodeposition of copper |
| US2873235A (en) * | 1957-06-19 | 1959-02-10 | Metal & Thermit Corp | Electrodeposition of copper |
| US3111465A (en) * | 1959-02-09 | 1963-11-19 | M & T Chemicals Inc | Electrodeposition of copper and copper alloys |
-
1964
- 1964-11-16 US US411543A patent/US3309293A/en not_active Expired - Lifetime
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2255057A (en) * | 1939-10-02 | 1941-09-09 | Du Pont | Electroplating copper |
| US2541700A (en) * | 1946-02-28 | 1951-02-13 | Du Pont | Electroplating copper |
| US2828252A (en) * | 1953-04-28 | 1958-03-25 | Degussa | Electrodeposition of bright zinc, copper, or nickel |
| US2765269A (en) * | 1954-11-19 | 1956-10-02 | Barnet D Ostrow | Bath for plating bright gold |
| US2817627A (en) * | 1955-07-11 | 1957-12-24 | Barnet D Ostrow | Process for plating bright brass |
| US2848394A (en) * | 1956-05-04 | 1958-08-19 | Hanson Van Winkle Munning Co | Bright copper plating |
| US2873234A (en) * | 1957-06-19 | 1959-02-10 | Metal & Thermit Corp | Electrodeposition of copper |
| US2873235A (en) * | 1957-06-19 | 1959-02-10 | Metal & Thermit Corp | Electrodeposition of copper |
| US3111465A (en) * | 1959-02-09 | 1963-11-19 | M & T Chemicals Inc | Electrodeposition of copper and copper alloys |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4376685A (en) * | 1981-06-24 | 1983-03-15 | M&T Chemicals Inc. | Acid copper electroplating baths containing brightening and leveling additives |
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