US2469727A - Electrodeposition of nickel - Google Patents
Electrodeposition of nickel Download PDFInfo
- Publication number
- US2469727A US2469727A US528776A US52877644A US2469727A US 2469727 A US2469727 A US 2469727A US 528776 A US528776 A US 528776A US 52877644 A US52877644 A US 52877644A US 2469727 A US2469727 A US 2469727A
- Authority
- US
- United States
- Prior art keywords
- nickel
- chloride
- sulfate
- naphthosultone
- sultone
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 title description 64
- 229910052759 nickel Inorganic materials 0.000 title description 32
- 238000004070 electrodeposition Methods 0.000 title description 9
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 21
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 21
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 20
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 19
- 150000008053 sultones Chemical class 0.000 description 18
- 238000007747 plating Methods 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- 238000007792 addition Methods 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 7
- 239000004327 boric acid Substances 0.000 description 7
- 150000002816 nickel compounds Chemical class 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- IEIADDVJUYQKAZ-UHFFFAOYSA-N 1,8-naphthosultone Chemical compound C1=CC(S(=O)(=O)O2)=C3C2=CC=CC3=C1 IEIADDVJUYQKAZ-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- MRXZEDMLQMDMGB-UHFFFAOYSA-N 3-formylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(C=O)=C1 MRXZEDMLQMDMGB-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- C25D3/12—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
- C25D3/18—Heterocyclic compounds
Definitions
- This invention relates to the electrodeposition of nickel and is more particularly concerned with nickel plating compositions, nickel plating baths, and processes for the electrodeposition of nickel wherein there is employed as an organic addition agent a sultone.
- the addition agents for use in nickel plating are characterized by the presence of the sultone group, as seen in 1,8-naphthosultone:
- 1,8-naphthosultone 1,8-naphthosultone- -sulfonic acid, 1,8-naphthosultone-3-sulfonic acid, and l,8-naphthosultone-3,6-disu1fonic acid.
- the sultones may be added to nickel plating baths as such or in the form of suitable salts, such as a sodium, potassium, ammonium, or nickel salts. Whether or not the sultone is present in the bath as a salt or as a free acid will depend upon the pH of the bath, and for the purposes of this application when reference is made to a sultone, it will be understood that any soluble salt may alternatively be used.
- suitable salts such as a sodium, potassium, ammonium, or nickel salts.
- the sultones may be used as addition agents in any of the nickel plating baths known to the art. There may be used for instance baths containing nickel sulfate, or nickel chloride, or mixtures of these nickel compounds preferably to-' gether with boric acid. Some of the best results are obtained with high chloride baths but the addition agents are quite satisfactory in sulfate baths containing relatively small amounts of chloride.
- Plating compositions may be oliered to the trade containing a sultone and one or more of the chemicals required to make up or to replenish a bright nickel plating bath.
- a sultone may, for instance, be packaged in a dry, prepared composition containing nickel sulfate, nickel chloride, or both, and may additionally contain wetting agents, other organic addition agents, or other desired bath additions.
- a typical dry packaged composition of the invention would contain from about /200 to part by weight of a sultone and the balance nickel sulfate, nickel chloride, or a mixture of them.
- Nickel sulfate "grams per liter 350 Nickel chloride do 15 Boric acid do 35 1,8-naphthosultone-4-su1fonic acid do 3 Temperature C' 50 pH 3.8
- Example II Nickel chloride grams per liter 250 Nickel sulphate do 15 Boric acid 50 1,8-naphthosultone-4-sulfonic acid do 4 Temperature C 50 pH 3.5
- Example VI Nickel chloride grands per liter 250 Nickel sulfate do Boric acid do 50 1,8-naphthosultone do 2 M-sulfobenzaldehyde do 2 Temperature C 50 pH 3.5
- the deposits obtained using the baths of the above examples are of increased brightness and ductility and the bright current density range is broadened by reason of the inclusion of a sultone.
- a nickel plating composition comprising a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel chloride and nickel sulfate, and /200 to /50 parts by Weight of a sultone.
- a nickel plating composition consisting of a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel chloride and nickel sulfate and /200 to /50 parts by Weight of 1,8-naphthosultone- 4-sulfonic acid.
- the step comprising electrodepositing nickel from an aqueous solution containing as electrolyte a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel sulfate and nickel chloride in the presence of one to ten grams per liter of a sultone.
- the step comprising electrodepositing nickel from an acidic aqueous solution containing as electrolyte a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel sulfate and nickel chloride in the presence of about 1 to 10 grams per liter of a sultone.
- the step comprising electrodepositing nickel from an acidic aqueous solution containing as electrolyte a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel sulfate and nickel chloride in the presence of about 1 to 10 grams er liter of 1,8-naphthosultone-4-sulfonic acid.
- the step comprising electrodepositing nickel from an acidic aqueous solution containing as electrolyte a major amount of nickel sulfate and a minor amount of nickel chloride in the presence of one to ten grams per liter of a sultone.
Landscapes
- 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
Patented May 10, 1949 ELEGTRODEPOSITION F NICKEL Raymond A. Hofiman, Euclid, Ohio,
E. I. du Font de Nemours & Company,
assignor to Wilmington, DeL, a corporation of Delaware No Drawing. ApplicationMarch 30, 1944, Serial No. 528,776
6 Claims.
This invention relates to the electrodeposition of nickel and is more particularly concerned with nickel plating compositions, nickel plating baths, and processes for the electrodeposition of nickel wherein there is employed as an organic addition agent a sultone.
It has already been proposed to electrodeposit nickel directly from a plating bath in a bright condition Processes for the direct deposition of bright nickel are particularly advantageous in the production of undercoats for chromium plating. By depositing the nickel in a bright condition the necessity for bufiing is eliminated and metal is, therefore, not removed as when an article is buffed. The time required for obtaining a finished product is reduced by producing bright nickel deposits directly from the bath and, perhaps most important of all, recesses inaccessible for bufiing are given a bright coat of nickel suitable as an ornamental finish or suitable as an undercoat for chromium.
It is an object of this invention to produce bright nickel deposits. It is a further object to provide dry plating compositions which upon being dissolved in water can be used for the electrodeposition of nickel deposits of improved character. It is a still further object to provide nickel plating processes which are simple and economical in operation and which produce bright ductile nickel deposits. It is a still further object to provide compositions, baths, and processes which permit the electrodeposition of nickel with a wider permissible range of electroplating bath constituents. Further objects will appear hereinafter.
The foregoing and other objects of the invention are attained by employing as an organic addition agent in nickel plating compositions, baths, and processes a sultone. More specifically, it has been found desirable to use 1,8-naphthosultonei-sulfonic acid.
The addition agents for use in nickel plating, according to the present invention, are characterized by the presence of the sultone group, as seen in 1,8-naphthosultone:
As illustrative of sultones, there may be mentioned 1,8-naphthosultone, 1,8-naphthosultone- -sulfonic acid, 1,8-naphthosultone-3-sulfonic acid, and l,8-naphthosultone-3,6-disu1fonic acid.
The sultones may be added to nickel plating baths as such or in the form of suitable salts, such as a sodium, potassium, ammonium, or nickel salts. Whether or not the sultone is present in the bath as a salt or as a free acid will depend upon the pH of the bath, and for the purposes of this application when reference is made to a sultone, it will be understood that any soluble salt may alternatively be used.
It will ordinarily be desirable to use from about 1 to 10 grams per liter of a sultone. More specifically, it has been found desirable to use from about 2 to 5 grams per liter of 1,8-naphthosultone-4sulfonic acid in a sulfate-nickel plating bath and about 3 to 8 grams per liter of the same agent in a high chloride nickel plating bath.
The sultones may be used as addition agents in any of the nickel plating baths known to the art. There may be used for instance baths containing nickel sulfate, or nickel chloride, or mixtures of these nickel compounds preferably to-' gether with boric acid. Some of the best results are obtained with high chloride baths but the addition agents are quite satisfactory in sulfate baths containing relatively small amounts of chloride.
While the sultones are quite effective alone and may satisfactorily be used as the sole organic addition agent for a nickel plating bath, it may sometimes be found desirable to use them in conjunction with organic addition agents, wetting agents, or metal brighteners in accordance with the practices already well known in the art.
Plating compositions, according to the present invention, may be oliered to the trade containing a sultone and one or more of the chemicals required to make up or to replenish a bright nickel plating bath. A sultone may, for instance, be packaged in a dry, prepared composition containing nickel sulfate, nickel chloride, or both, and may additionally contain wetting agents, other organic addition agents, or other desired bath additions. A typical dry packaged composition of the invention would contain from about /200 to part by weight of a sultone and the balance nickel sulfate, nickel chloride, or a mixture of them.
In order that the invention may be better understood, reference should be had to the following illustrative examples.
Example I Nickel sulfate "grams per liter 350 Nickel chloride do 15 Boric acid do 35 1,8-naphthosultone-4-su1fonic acid do 3 Temperature C' 50 pH 3.8
Example II Nickel chloride grams per liter 250 Nickel sulphate do 15 Boric acid 50 1,8-naphthosultone-4-sulfonic acid do 4 Temperature C 50 pH 3.5
Easample III Nickel sulfate grams per liter 350 Nickel chloride do 15 Boric acid do 35 1,8-naphthosultone-4sulfonic acid do 2 M-sulfobenzaldehyde do 1 Temperature C 50 pH 3.8
Example IV Nickel chloride grams per liter 250 Nickel sulfate do 15 Boric acid do 50 1,8-Naphthosultone-4-sulfonic acid do 2 M-sulfobenzaldehyde do 2 Temperature C 50 pH 3.5
Example V Nickel sulfate grams per liter 350 Nickel chloride do 15 Boric acid d 35 1,8-naphthosultone do 2 M'-sulfobenzaldehyde do 2 Temperature C 50 pH 3.8
Example VI Nickel chloride grands per liter 250 Nickel sulfate do Boric acid do 50 1,8-naphthosultone do 2 M-sulfobenzaldehyde do 2 Temperature C 50 pH 3.5 The deposits obtained using the baths of the above examples are of increased brightness and ductility and the bright current density range is broadened by reason of the inclusion of a sultone.
I claim:
1. A nickel plating composition comprising a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel chloride and nickel sulfate, and /200 to /50 parts by Weight of a sultone.
2. A nickel plating composition consisting of a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel chloride and nickel sulfate and /200 to /50 parts by Weight of 1,8-naphthosultone- 4-sulfonic acid.
3. In a process for the electrodeposition of nickel, the step comprising electrodepositing nickel from an aqueous solution containing as electrolyte a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel sulfate and nickel chloride in the presence of one to ten grams per liter of a sultone.
4. In a process for the electrodeposition of nickel, the step comprising electrodepositing nickel from an acidic aqueous solution containing as electrolyte a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel sulfate and nickel chloride in the presence of about 1 to 10 grams per liter of a sultone.
5. In a process for the electrodeposition of nickel, the step comprising electrodepositing nickel from an acidic aqueous solution containing as electrolyte a nickel compound selected from the group consisting of nickel sulfate, nickel chloride, and mixtures of nickel sulfate and nickel chloride in the presence of about 1 to 10 grams er liter of 1,8-naphthosultone-4-sulfonic acid.
6. In a process for the electrodeposition of nickel, the step comprising electrodepositing nickel from an acidic aqueous solution containing as electrolyte a major amount of nickel sulfate and a minor amount of nickel chloride in the presence of one to ten grams per liter of a sultone.
RAYMOND A. HOFFMAN.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,112,818 Waite Mar. 29, 1938 2,338,529 Mougey et al Jan. 4, 1944 2,359,730 Schetty Oct. 3, 1944
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US528776A US2469727A (en) | 1944-03-30 | 1944-03-30 | Electrodeposition of nickel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US528776A US2469727A (en) | 1944-03-30 | 1944-03-30 | Electrodeposition of nickel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2469727A true US2469727A (en) | 1949-05-10 |
Family
ID=24107146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US528776A Expired - Lifetime US2469727A (en) | 1944-03-30 | 1944-03-30 | Electrodeposition of nickel |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2469727A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2539588A (en) * | 1949-02-17 | 1951-01-30 | Harshaw Chem Corp | Electrodeposition of nickel |
| US2876177A (en) * | 1955-03-16 | 1959-03-03 | Dehydag Gmbh | Additives for nickel electroplating baths |
| US3041255A (en) * | 1960-03-22 | 1962-06-26 | Metal & Thermit Corp | Electrodeposition of bright nickel |
| US3423296A (en) * | 1964-10-08 | 1969-01-21 | Enthone | Nickel electrodepositing baths,process,and additive composition comprising levelling agent therefor |
| US3457146A (en) * | 1964-10-08 | 1969-07-22 | Enthone | Process of electrodepositing nickel and electrolyte and additive composition therefor |
| US3856638A (en) * | 1971-08-20 | 1974-12-24 | Auric Corp | Bright gold electroplating bath and method of electroplating bright gold |
| US4077855A (en) * | 1976-05-04 | 1978-03-07 | Francine Popescu | Bright nickel electroplating bath and process |
| US4199416A (en) * | 1977-05-03 | 1980-04-22 | Johnson, Matthey & Co., Limited | Composition for the electroplating of gold |
| US4376018A (en) * | 1979-12-31 | 1983-03-08 | Bell Telephone Laboratories, Incorporated | Electrodeposition of nickel |
| US4715935A (en) * | 1985-01-25 | 1987-12-29 | Omi International Corporation | Palladium and palladium alloy plating |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2112818A (en) * | 1934-08-15 | 1938-03-29 | Mcgean Chem Co Inc | Electrodeposition of metals |
| US2338529A (en) * | 1936-06-08 | 1944-01-04 | Gen Motors Corp | Electrodeposition of nickel |
| US2359730A (en) * | 1942-10-02 | 1944-10-03 | Swiss Firm Of J R Geigy A G | Derivatives of naphthosultones and a process for their manufacture |
-
1944
- 1944-03-30 US US528776A patent/US2469727A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2112818A (en) * | 1934-08-15 | 1938-03-29 | Mcgean Chem Co Inc | Electrodeposition of metals |
| US2338529A (en) * | 1936-06-08 | 1944-01-04 | Gen Motors Corp | Electrodeposition of nickel |
| US2359730A (en) * | 1942-10-02 | 1944-10-03 | Swiss Firm Of J R Geigy A G | Derivatives of naphthosultones and a process for their manufacture |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2539588A (en) * | 1949-02-17 | 1951-01-30 | Harshaw Chem Corp | Electrodeposition of nickel |
| US2876177A (en) * | 1955-03-16 | 1959-03-03 | Dehydag Gmbh | Additives for nickel electroplating baths |
| US3041255A (en) * | 1960-03-22 | 1962-06-26 | Metal & Thermit Corp | Electrodeposition of bright nickel |
| US3423296A (en) * | 1964-10-08 | 1969-01-21 | Enthone | Nickel electrodepositing baths,process,and additive composition comprising levelling agent therefor |
| US3457146A (en) * | 1964-10-08 | 1969-07-22 | Enthone | Process of electrodepositing nickel and electrolyte and additive composition therefor |
| US3856638A (en) * | 1971-08-20 | 1974-12-24 | Auric Corp | Bright gold electroplating bath and method of electroplating bright gold |
| US4077855A (en) * | 1976-05-04 | 1978-03-07 | Francine Popescu | Bright nickel electroplating bath and process |
| US4199416A (en) * | 1977-05-03 | 1980-04-22 | Johnson, Matthey & Co., Limited | Composition for the electroplating of gold |
| US4376018A (en) * | 1979-12-31 | 1983-03-08 | Bell Telephone Laboratories, Incorporated | Electrodeposition of nickel |
| US4715935A (en) * | 1985-01-25 | 1987-12-29 | Omi International Corporation | Palladium and palladium alloy plating |
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