US3305461A - Nickel electroplating bath with additives - Google Patents
Nickel electroplating bath with additives Download PDFInfo
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- US3305461A US3305461A US304270A US30427063A US3305461A US 3305461 A US3305461 A US 3305461A US 304270 A US304270 A US 304270A US 30427063 A US30427063 A US 30427063A US 3305461 A US3305461 A US 3305461A
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- Prior art keywords
- mercapto
- acetylenic
- nickel
- compounds
- additives
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- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 title claims description 51
- 229910052759 nickel Inorganic materials 0.000 title claims description 25
- 239000000654 additive Substances 0.000 title description 5
- 238000009713 electroplating Methods 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 18
- 238000007747 plating Methods 0.000 claims description 16
- 239000011260 aqueous acid Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 8
- HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical class SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 description 8
- NIAGBSSWEZDNMT-UHFFFAOYSA-N hydroxidotrioxidosulfur(.) Chemical class [O]S(O)(=O)=O NIAGBSSWEZDNMT-UHFFFAOYSA-N 0.000 description 6
- 150000003230 pyrimidines Chemical class 0.000 description 6
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 6
- -1 sulfonated aryl aldehydes Chemical class 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 241000080590 Niso Species 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000011133 lead Substances 0.000 description 3
- 239000002932 luster Substances 0.000 description 3
- 150000003460 sulfonic acids Chemical class 0.000 description 3
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
- UJHVKLMYJAONMU-UHFFFAOYSA-N 4,4,6-trimethyl-2,3-dihydro-1h-pyrimidine Chemical compound CC1=CC(C)(C)NCN1 UJHVKLMYJAONMU-UHFFFAOYSA-N 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000005282 brightening Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 description 2
- XTEGVFVZDVNBPF-UHFFFAOYSA-N naphthalene-1,5-disulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1S(O)(=O)=O XTEGVFVZDVNBPF-UHFFFAOYSA-N 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- SAITXBOGTNNNJW-UHFFFAOYSA-N 1,2-dihydropyrimidine-2-thiol Chemical compound SC1NC=CC=N1 SAITXBOGTNNNJW-UHFFFAOYSA-N 0.000 description 1
- QXTDXPHVQQCKEK-UHFFFAOYSA-N 1,4-diethoxybut-2-yne-1,1-diol Chemical compound C(C)OC(C#CCOCC)(O)O QXTDXPHVQQCKEK-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- JQZGUQIEPRIDMR-UHFFFAOYSA-N 3-methylbut-1-yn-1-ol Chemical compound CC(C)C#CO JQZGUQIEPRIDMR-UHFFFAOYSA-N 0.000 description 1
- XRVWIVBMIGIJHG-UHFFFAOYSA-N 4,6-dimethyl-1,2-dihydropyrimidine Chemical compound CC1=CC(C)=NCN1 XRVWIVBMIGIJHG-UHFFFAOYSA-N 0.000 description 1
- 240000005020 Acaciella glauca Species 0.000 description 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- SYBUMOIKKHDLBN-UHFFFAOYSA-N C(=C)S(=O)(=O)O.C1=CC=CC=C1 Chemical compound C(=C)S(=O)(=O)O.C1=CC=CC=C1 SYBUMOIKKHDLBN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-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
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- DLDJFQGPPSQZKI-UHFFFAOYSA-N but-2-yne-1,4-diol Chemical compound OCC#CCO DLDJFQGPPSQZKI-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 125000001145 hydrido group Chemical group *[H] 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- GPUMPJNVOBTUFM-UHFFFAOYSA-N naphthalene-1,2,3-trisulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC2=C1 GPUMPJNVOBTUFM-UHFFFAOYSA-N 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- TVDSBUOJIPERQY-UHFFFAOYSA-N prop-2-yn-1-ol Chemical compound OCC#C TVDSBUOJIPERQY-UHFFFAOYSA-N 0.000 description 1
- KZVLNAGYSAKYMG-UHFFFAOYSA-N pyridine-2-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=N1 KZVLNAGYSAKYMG-UHFFFAOYSA-N 0.000 description 1
- ZKIHLVYBGPFUAD-UHFFFAOYSA-N quinoline-2-sulfonic acid Chemical compound C1=CC=CC2=NC(S(=O)(=O)O)=CC=C21 ZKIHLVYBGPFUAD-UHFFFAOYSA-N 0.000 description 1
- 235000003499 redwood Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940075560 sodium lauryl sulfoacetate Drugs 0.000 description 1
- 229940067741 sodium octyl sulfate Drugs 0.000 description 1
- UAJTZZNRJCKXJN-UHFFFAOYSA-M sodium;2-dodecoxy-2-oxoethanesulfonate Chemical compound [Na+].CCCCCCCCCCCCOC(=O)CS([O-])(=O)=O UAJTZZNRJCKXJN-UHFFFAOYSA-M 0.000 description 1
- HRQDCDQDOPSGBR-UHFFFAOYSA-M sodium;octane-1-sulfonate Chemical compound [Na+].CCCCCCCCS([O-])(=O)=O HRQDCDQDOPSGBR-UHFFFAOYSA-M 0.000 description 1
- WFRKJMRGXGWHBM-UHFFFAOYSA-M sodium;octyl sulfate Chemical compound [Na+].CCCCCCCCOS([O-])(=O)=O WFRKJMRGXGWHBM-UHFFFAOYSA-M 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- 229960001124 trientine Drugs 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
- C25D3/12—Electroplating: Baths therefor from solutions of nickel or cobalt
- C25D3/14—Electroplating: Baths therefor from solutions of nickel or cobalt from baths containing acetylenic or heterocyclic compounds
Definitions
- this concentration of acetylenic derivatives is such that the low current density areas for example, areas as loW as 1 amp/sq. ft. or less are then not covered by the nickel electroplate. Since in modern electroplating it is essential from a commercially feasible application to have the nickel electroplate cover the low current density areas, as Well as the high, it becomes necessary frequently to operate these nickel'baths with less than the optimum concentration of the acetylenic compounds in order to secure coverage in these low current densities. This, of course, results in deposits that do not have the maximum leveling or brightening rate.
- acetylenic compounds When the acetylenic compounds are added to the bath at their optimum concentration, or in excess of the optimum concentration, in addition to skipping, these high concentrations of acetylenic compounds also impart hazes and clouds to the deposit. These hazes and clouds are sometimes corrected by the addition of sulfooxygen compounds. These compounds must generally be added in fairly large quantities and they in turn adversely afiect the leveling. In any event the sulfo-oxygen compounds do not overcome the tendency to skip, whereas they may correct the clouding and hazing concentrations.
- the present invention is adapted and intended to overcome the difiiculties inherent in prior compositions of the type discussed above, it being among the objects of the invention to provide an aqueous acid nickel plating bath having certain additives therein which will avoid skipping in the low current density areas.
- the combination of mercapto alkyl hydropyrimidines in conjunction with acetylenic compounds overcome the tendency for these compounds to skip.
- the alkyl groups have from 1 to 4 carbon atoms.
- the acetylenic derivatives in conjunction with the mercapto alkyl pyrimidines produce bright plate without haze, cloud and skip, without impairment of the leveling characteristics.
- the combination of the mercapto pyrimidines with the acetylenic derivatives and the sulfo-oxygen compound will produce deposits that are level and bright, without any of the aforementioned undesirable characteristics.
- the tolerance of the acetylenic base baths to zinc, copper or lead is greatly enhanced by the addition of the mercapto pyrimidine. Since the mercapto pyrimidines are not too soluble in the system, we prefer to use the sulfonated or sulfated type of derivatives. It is only through the combination of these three ingredients that the maximum improvements can be secured.
- sulfo-oxygen compounds are such sulfonamids and sulfonimides as o-benzene sulfonimid (Na salt), benzene sulfonamid, dibenzene sulfonimid, p-toluene sulfonamid, benzene sulfahydroxamic acid (Na salt), and allyl sulfonamid.
- sulfonic acids are naphthalene trisulfonic acid (Na salt), benzene sulfonic acid (Ni salt), benzene vinyl sulfonic acid (Na salt), allyl sulfonic acid (Na salt), naphthalene 1,5 disulfonic acid (Na salt), l-butene sulfonic acid, quinoline sulfonic acid, and pyridine sulfonic acid.
- Na salt naphthalene trisulfonic acid
- benzene sulfonic acid Na salt
- benzene vinyl sulfonic acid Na salt
- allyl sulfonic acid Na salt
- naphthalene 1,5 disulfonic acid Na salt
- l-butene sulfonic acid quinoline sulfonic acid
- pyridine sulfonic acid Of the above sulfonamids and sulfonimids are presently preferred.
- Typical acetylenic derivatives are Z-methyl 3-butyne 2-01, 1,4 butyne diol, 1,4 diethoxy butyne diol, propargyl alcohol, butynoxyacetic acid, N,N,N propargyl triethylene tetramine, and N,N,N propargyl diethylene triamine.
- Typical mercapto pyrimidines includes '2-mercapto 4,6 diethyl 4-methyl dihydro pyrimidine, sulfonated 2-mercapto 4,6 diethyl 4-methyl dihydro pyrimidine, Z-mercapto 4,4,6 trimethyl dihydro pyrimidine, Z-mercapto 4,6 dimethyl dihydro pyrimidine, and sulfonated Z-mercapto 4,4,6 trimethyl dihydropyrimidine.
- NiSO '6H O g./1. 100-300 NiCl -6H O, g./l. 30-100 H BO g./l. 2060 pH 3.0-4.8
- the preferred bath is one with NiSO '6H O 300 g./l., NiCl -6H O 90 g./l., H 80 45 g./l., pH 4.0-4.5, and temperature l35140 F. with mild agitation.
- surface active agents as are commonly employed in the art to decrease surface tension and reduce pitting.
- surfactants are sodium lauryl sulfate, sodium octyl sulfate, sodium octyl sulfonate, and sodium lauryl sulfoacetate.
- the mercapto pyrimidines may be used in concentrations as low as 0.001 gram per liter.
- the amounts of sulfonamides, sulfonamids and the sulfonic acids may be present in the solution in the bath in amounts of about 0.2 gram per liter and up to saturation. The higher concentrations will be determined by the quantity of acetylenic compound that is present in the bath as well as the type of acetylenic compound. Generally a sufficient quantity of the mercapto pyrimidine is added to overcome the skipping or low current density problem.
- the standard Watts type solution containing 1 gram per liter of saccharine and 0.4 gram per liter of methylbutynol, with the nickel solution being agitated will show a tendency toward low current density skipping.
- the addition of 0.01 gram per liter of the sulfonated derivative of 4,4,6,trimethyl 2-mercapto dihydropyrimidine will increase the coverage of the nickel in the low current density, substantially eliminating the skip without impairing the luster and level of the bright nickel plate.
- the concentrations of the several additives may be greatly varied as other concentrations than those set forth are workable with good effects.
- the preferred range of the acetylenic compound is from .001 to 1.0 gram per liter, and the concentration of the mercapto pyrimidine is from .001 to 1.0 gram per liter, but the invention is not restricted to these specific amounts.
- An aqueous acid nickel plating bath having incorporated therein a water soluble acetylenic compound and a water-soluble mercapto alkyl hydropyrimidine, the amount of said compounds being sufficient to prevent skip plate in low current density areas.
- a nickel plating bath according to claim 1 characterized in that said bath contains also a substance taken from the class consisting of aromatic sulfonamids, sulfonimids, and sulfonic acids in sufficient amounts to produce leveling of deposits without clouding.
- a nickel plating bath according to claim 2 characterized in that said substance is present in amounts of 0.2 gram per liter to saturation.
- a nickel plating bath according to claim 2 characterized in that said acetylenic compound is present in amounts of .001 to 1.0 gram per liter.
- a nickel plating bath according to claim 2 characterized in that said mercapto-pyrimidine is present in amounts of .001 to 1.0 gram per liter.
- a nickel plating bath according to claim 1 characterized in that said acetylenic compound is present in amounts of .001 to 1.0 gram per liter.
- a nickel plating bath according to claim 1 characterized in that said mercapto-pyrirnidine is present in amounts of .001 to 1.0 gram per liter.
- a nickel plating bath according to claim 1 characterized in that said pyrimidine contains at least one hydro group.
- a nickel plating bath according to claim 1 characterized in that said pyrimidine contains a plurality of alkyl groups.
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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)
- Electroplating And Plating Baths Therefor (AREA)
Description
Un ted t es. P te Q I 3,305,461 NICKEL ELECTRORLATING BATH WITH ADDITIVES Barnet l). Ostrow, 125 Redwood Drive, and Fred I. Nobel, 75 Fem Drive, both of Roslyn, NY. 11576 No Drawing. Filed Aug. 23, 1963, Ser. No. 304,270 9 Claims. (Cl. 204-49) the major difiiculties associated with nickel baths emacetylenic derivatives are exceptionally prone to skipping, clouding and hazing. By skipping is meant, the inability of the nickel electroplating bath to cover with nickel, parts in low current density areas.
There has been described the addition to the bath of thiomalic acid to overcome this difiiculty. It has been found, however, that compounds of this category are not eiiective in overcoming such skipping tendencies. Although the thiomalic acids increase the tolerance of the electroplating bath to such metallic impurities as lead and Zinc, it will not overcome the skipping tendencies that are imparted by higher concentrations of acetylenic derivatives. Since the acetylenic derivatives impart the maximum luster and leveling to the plating bath, it is desirable to keep them in a fairly high concentration to obtain the optimum brilliance and leveling. In many cases this concentration of acetylenic derivatives is such that the low current density areas for example, areas as loW as 1 amp/sq. ft. or less are then not covered by the nickel electroplate. Since in modern electroplating it is essential from a commercially feasible application to have the nickel electroplate cover the low current density areas, as Well as the high, it becomes necessary frequently to operate these nickel'baths with less than the optimum concentration of the acetylenic compounds in order to secure coverage in these low current densities. This, of course, results in deposits that do not have the maximum leveling or brightening rate.
When the acetylenic compounds are added to the bath at their optimum concentration, or in excess of the optimum concentration, in addition to skipping, these high concentrations of acetylenic compounds also impart hazes and clouds to the deposit. These hazes and clouds are sometimes corrected by the addition of sulfooxygen compounds. These compounds must generally be added in fairly large quantities and they in turn adversely afiect the leveling. In any event the sulfo-oxygen compounds do not overcome the tendency to skip, whereas they may correct the clouding and hazing concentrations.
In modern bright nickel plating, the acetylenic derivatives, even in lower than optimum concentration, may
3,335,461 Patented Feb. 21, .1967
under electrolysis, form degradation productions that tend to give gray to black low current density recessed areas.
This condition is particularly more pronounced when trace amounts of zinc, lead or copper are present as impurities. Since commercial bright nickel plating involves plating of zinc die castings, as well as copper plated and copper base metal parts, the tendency for contamination with these metals, is always present and may become serious.
In US. Patent No. 2,361,720, it has been suggested that thiopyrimidines be used in nickel plating baths as brightening agents. Specifically a compound mentioned has been 2 mercapto-4,6,alkyl-6-dihydroxypyrimidine. To increase the solubility, these products are sul-fated or sulfonated. In addition, the use of the aforementioned pyrimidines in conjunction with sulfonated aryl aldehydes has been described. Although the pyrimidines and the pyrimidines in combination with sulfonated aryl aldehydes produced bright plate, these deposits exhibited no leveling. Actually, the pyrimidines, when used in concentrations sufiicient to impart overall brightness, tended to produce negative leveling. When used in conjunction with sulfo-oxygen compounds, the pyrimidines behaved in a similar manner.
The present invention is adapted and intended to overcome the difiiculties inherent in prior compositions of the type discussed above, it being among the objects of the invention to provide an aqueous acid nickel plating bath having certain additives therein which will avoid skipping in the low current density areas.
It is also among the objects of the invention to provide such a composition which will prevent or at least greatly limit the tendency of baths of this type to form hazy or cloudy depositsf It is further'among the objects of the present inven tion to provide such a composition which will impart to the deposit a maximum of luster and a high degree of leveling.
It has now been found that the combination of mercapto alkyl hydropyrimidines in conjunction with acetylenic compounds, overcome the tendency for these compounds to skip. Usually the alkyl groups have from 1 to 4 carbon atoms. In addition, when used in combination with sulfo-oxygen compounds, the acetylenic derivatives in conjunction with the mercapto alkyl pyrimidines produce bright plate without haze, cloud and skip, without impairment of the leveling characteristics. Therefore, unlike the pyrimidines used in conjunction with suite-oxygen compounds alone, the combination of the mercapto pyrimidines with the acetylenic derivatives and the sulfo-oxygen compound, will produce deposits that are level and bright, without any of the aforementioned undesirable characteristics. The tolerance of the acetylenic base baths to zinc, copper or lead is greatly enhanced by the addition of the mercapto pyrimidine. Since the mercapto pyrimidines are not too soluble in the system, we prefer to use the sulfonated or sulfated type of derivatives. It is only through the combination of these three ingredients that the maximum improvements can be secured.
Compounds typical of the sulfo-oxygen compounds are such sulfonamids and sulfonimides as o-benzene sulfonimid (Na salt), benzene sulfonamid, dibenzene sulfonimid, p-toluene sulfonamid, benzene sulfahydroxamic acid (Na salt), and allyl sulfonamid. Among sulfonic acids are naphthalene trisulfonic acid (Na salt), benzene sulfonic acid (Ni salt), benzene vinyl sulfonic acid (Na salt), allyl sulfonic acid (Na salt), naphthalene 1,5 disulfonic acid (Na salt), l-butene sulfonic acid, quinoline sulfonic acid, and pyridine sulfonic acid. Of the above sulfonamids and sulfonimids are presently preferred.
Typical acetylenic derivatives are Z-methyl 3-butyne 2-01, 1,4 butyne diol, 1,4 diethoxy butyne diol, propargyl alcohol, butynoxyacetic acid, N,N,N propargyl triethylene tetramine, and N,N,N propargyl diethylene triamine. Typical mercapto pyrimidines includes '2-mercapto 4,6 diethyl 4-methyl dihydro pyrimidine, sulfonated 2-mercapto 4,6 diethyl 4-methyl dihydro pyrimidine, Z-mercapto 4,4,6 trimethyl dihydro pyrimidine, Z-mercapto 4,6 dimethyl dihydro pyrimidine, and sulfonated Z-mercapto 4,4,6 trimethyl dihydropyrimidine.
These combinations may be included in a standard Watts Formulation of the following composition or in a high chloride formulation of the following type of composition.
NiSO '6H O, g./1. 100-300 NiCl -6H O, g./l. 30-100 H BO g./l. 2060 pH 3.0-4.8
Temperature, F.
The preferred bath is one with NiSO '6H O 300 g./l., NiCl -6H O 90 g./l., H 80 45 g./l., pH 4.0-4.5, and temperature l35140 F. with mild agitation. To the baths above is added such surface active agents as are commonly employed in the art to decrease surface tension and reduce pitting. Examples of such surfactants are sodium lauryl sulfate, sodium octyl sulfate, sodium octyl sulfonate, and sodium lauryl sulfoacetate.
The mercapto pyrimidines may be used in concentrations as low as 0.001 gram per liter. The amounts of sulfonamides, sulfonamids and the sulfonic acids may be present in the solution in the bath in amounts of about 0.2 gram per liter and up to saturation. The higher concentrations will be determined by the quantity of acetylenic compound that is present in the bath as well as the type of acetylenic compound. Generally a sufficient quantity of the mercapto pyrimidine is added to overcome the skipping or low current density problem. For example, the standard Watts type solution containing 1 gram per liter of saccharine and 0.4 gram per liter of methylbutynol, with the nickel solution being agitated, will show a tendency toward low current density skipping. The addition of 0.01 gram per liter of the sulfonated derivative of 4,4,6,trimethyl 2-mercapto dihydropyrimidine will increase the coverage of the nickel in the low current density, substantially eliminating the skip without impairing the luster and level of the bright nickel plate.
Using a bath of the following composition will illustrate the combination usage of these additives:
G./l. NiSO -7H O 300 NiCl -6H O 45 H3BO3 45 Sodium lauryl sulfate 0.2
Grams Per Liter The concentrations of the several additives may be greatly varied as other concentrations than those set forth are workable with good effects. The preferred range of the acetylenic compound is from .001 to 1.0 gram per liter, and the concentration of the mercapto pyrimidine is from .001 to 1.0 gram per liter, but the invention is not restricted to these specific amounts.
What is claimed is:
1. An aqueous acid nickel plating bath having incorporated therein a water soluble acetylenic compound and a water-soluble mercapto alkyl hydropyrimidine, the amount of said compounds being sufficient to prevent skip plate in low current density areas.
2. A nickel plating bath according to claim 1 characterized in that said bath contains also a substance taken from the class consisting of aromatic sulfonamids, sulfonimids, and sulfonic acids in sufficient amounts to produce leveling of deposits without clouding.
3. A nickel plating bath according to claim 2 characterized in that said substance is present in amounts of 0.2 gram per liter to saturation.
4. A nickel plating bath according to claim 2 characterized in that said acetylenic compound is present in amounts of .001 to 1.0 gram per liter.
5. A nickel plating bath according to claim 2 characterized in that said mercapto-pyrimidine is present in amounts of .001 to 1.0 gram per liter.
6. A nickel plating bath according to claim 1 characterized in that said acetylenic compound is present in amounts of .001 to 1.0 gram per liter.
7. A nickel plating bath according to claim 1 characterized in that said mercapto-pyrirnidine is present in amounts of .001 to 1.0 gram per liter.
8. A nickel plating bath according to claim 1 characterized in that said pyrimidine contains at least one hydro group.
9. A nickel plating bath according to claim 1 characterized in that said pyrimidine contains a plurality of alkyl groups.
References Cited by the Examiner UNITED STATES PATENTS HOWARD S. WILLIAMS, Primary Examiner. JOHN H. MACK, Examiner.
G. KAPLAN, Assistant Examiner.
Claims (1)
1. AN AQUEOUS ACID NICKEL PLATING BATH HAVING INCORPORATED THEREIN A WATER SOLUBLE ACETYLENIC COMPOUND AND A WATER-SOLUBLE MERCAPTO ALKYL HYDROPYRIMIDINE, THE AMOUNT OF SAID COMPOUNDS BEING SUFFICIENT TO PREVENT SKIP PLATE IN LOW CURRENT DENSITY AREAS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US304270A US3305461A (en) | 1963-08-23 | 1963-08-23 | Nickel electroplating bath with additives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US304270A US3305461A (en) | 1963-08-23 | 1963-08-23 | Nickel electroplating bath with additives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3305461A true US3305461A (en) | 1967-02-21 |
Family
ID=23175790
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US304270A Expired - Lifetime US3305461A (en) | 1963-08-23 | 1963-08-23 | Nickel electroplating bath with additives |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3305461A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3661731A (en) * | 1970-03-16 | 1972-05-09 | Allied Chem | Electrodeposition of bright nickel |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2361720A (en) * | 1942-02-21 | 1944-10-31 | Us Rubber Co | Nickel electroplating bath |
| US2485149A (en) * | 1944-04-17 | 1949-10-18 | Seymour Mfg Company | Bright nickel plating compositions and process |
| US2712522A (en) * | 1953-03-24 | 1955-07-05 | Hanson Van Winkle Munning Co | Bright nickel plating |
| US2818376A (en) * | 1956-12-28 | 1957-12-31 | Hanson Van Winkle Munning Co | Nickel plating |
| US3002904A (en) * | 1958-09-26 | 1961-10-03 | Hanson Van Winkle Munning Co | Electrodeposition of nickel |
-
1963
- 1963-08-23 US US304270A patent/US3305461A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2361720A (en) * | 1942-02-21 | 1944-10-31 | Us Rubber Co | Nickel electroplating bath |
| US2485149A (en) * | 1944-04-17 | 1949-10-18 | Seymour Mfg Company | Bright nickel plating compositions and process |
| US2712522A (en) * | 1953-03-24 | 1955-07-05 | Hanson Van Winkle Munning Co | Bright nickel plating |
| US2818376A (en) * | 1956-12-28 | 1957-12-31 | Hanson Van Winkle Munning Co | Nickel plating |
| US3002904A (en) * | 1958-09-26 | 1961-10-03 | Hanson Van Winkle Munning Co | Electrodeposition of nickel |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3661731A (en) * | 1970-03-16 | 1972-05-09 | Allied Chem | Electrodeposition of bright nickel |
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