US3767540A - Additive for electrodeposition of bright zinc from aqueous, acid, electroplating baths - Google Patents
Additive for electrodeposition of bright zinc from aqueous, acid, electroplating baths Download PDFInfo
- Publication number
- US3767540A US3767540A US00296826A US3767540DA US3767540A US 3767540 A US3767540 A US 3767540A US 00296826 A US00296826 A US 00296826A US 3767540D A US3767540D A US 3767540DA US 3767540 A US3767540 A US 3767540A
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- United States
- Prior art keywords
- zinc
- acid
- aqueous
- bright
- electrodeposition
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- 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
Definitions
- ABSTRACT It has been found that upon addition to an aqueous, acid, zinc electroplating bath, naphthol polyoxyalkylate and polyethylenimine act synergistically to provide smooth, bright, ductile, electrodeposits of zinc.
- This invention pertains to improvements in the electrodeposition of bright zinc from aqueous acid plating baths.
- Acid zinc electroplating baths are not new in the plating field and have, in fact, been used with moderate success for quite some time. Prior to this invention, however, certain limitations have in many instances rendered the existing acid zinc plating bath compositions extremely impractical to use and quite often not applicable at all.
- Another problem that has been common has been the lack of ductility in the zinc plate obtained from existing acid zinc bath compositions. Many parts are bent or shaped after plating either through manufacturing processes or through normal use. If the electrodeposit is not reasonably ductile, chipping, flaking and peeling of the plate canoccur, thus causing rejection of the part.
- the additionagents and bath compositions of this invention have overcome these serious limitations. With the use of this invention, mugh higher current densities and operating temperatures can be used to obtain lustrous, bright, ductile deposits of zinc from acid zinc plating baths. This is possible because these additives provide bright deposits over a very wide current density range, are'chemically stable, and are not adversely affected by normal increases in temperature.
- R is hydrogen and methyl, and x is about 8 to 20.
- polyethylenimine having the formula:
- R is hydrogen, methyl, ethyl, propyl, hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 2- aminoethyl, Z-aminopropyl, and 3-aminopropy1, and y is about 10 to 20.
- the present invention is also an addition agent for an acid zinc electroplating bath consisting of from about 1:100 to :1 parts by weight of naphthol polyoxyalkylate and polyethylenimine of the above formulae.
- a general purpose bath was made up which contained 30 gms. ZnCl /liter and 200 gms. NH Cl/liter at a pH of 4.9.
- the current density area from 0 to 50 amps per sq. ft. is left as a dark, rough electrodeposit with no trace of brightness.
- the naphthol polyoxyalkylate and the polyethylenimine act synergistically to provide a bright, lustrous electrodeposit from about 12 amps per sq. ft. to well over 200 amps per sq. ft. In addition to being extremely bright, the deposit is quite ductile.
- the current densities below 12 amps per sq. ft. can be made bright by the addition of between 0.01 and 10 gms. per liter of a substance selected from the group consisting of anisaldehyde, piperonal, veratraldehyde, benzaldehyde, vanillan, benzylidene acetone, and cinnamic aldehyde.
- An addition agent for an acid zinc electroplating bath consisting of from about 1:100 to about parts by weight of naphthol polyoxyalkylate having the formula:
- R is hydrogen, methyl, ethyl propyl, hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 2- aminoethyl, 2-aminopropyl, and 3-aminopropyl, and y is about 10 to about 20.
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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)
Abstract
It has been found that upon addition to an aqueous, acid, zinc electroplating bath, naphthol polyoxyalkylate and polyethylenimine act synergistically to provide smooth, bright, ductile, electrodeposits of zinc.
Description
United States Patent Rosenberg 1 Oct. 23, 1973 ADDITIVE FOR ELECTRODEPOSITION OF BRIGHT ZINC FROM AQUEOUS, ACID, ELECTROPLATING BATHS William E. Rosenberg, Parma, Ohio Assignee: R. 0. Hull & Company, Inc.,
Cleveland, Ohio Filed: Oct. 12, 1972 Appl. No.: 296,826
Related U.S. Application Data Division of Ser. No. 229,590, Feb. 25, 1972, Pat. No. 3,723,263.
Inventor:
U.S. c1. 204/55 R, 204/DIG. 2 Int. Cl. c231, 5/46 Field of Search 204/55 R, 55 Y, 43,
204/44, 45 R, 45 A, 46, 47, 48, 49, 50 R, 50 Y, 51, 52 R, 52 Y, 53,54 R, 54 L, DIG. 2
Primary Examiner-G. L. Kaplan Att0rneyBlythe D. Watts et al.
[57] ABSTRACT It has been found that upon addition to an aqueous, acid, zinc electroplating bath, naphthol polyoxyalkylate and polyethylenimine act synergistically to provide smooth, bright, ductile, electrodeposits of zinc.
1 Claim, No Drawings ADDI'TIVE FOR ELECTRODEPOSITION F BRIGHT ZINC FROM AQUEOUS, ACID, ELECTROPLATING BATI-IS This application is a division of my copending U.S. Pat. application, Ser. No. 229,590, filed Feb. 25, 1972, now U.S. Pat. No. 3,723,263.
BACKGROUND OF THE INVENTION This invention pertains to improvements in the electrodeposition of bright zinc from aqueous acid plating baths.
Acid zinc electroplating baths are not new in the plating field and have, in fact, been used with moderate success for quite some time. Prior to this invention, however, certain limitations have in many instances rendered the existing acid zinc plating bath compositions extremely impractical to use and quite often not applicable at all.
One of the most limiting factors in the plating of bright zinc from acid plating baths has been that only a rather low current density could be applied to a given part to produce a lustrous zinc deposit. By raising the current density to increase the speed of plating, the platr would encounter dark, coarse, and even spongy deposits of zinc.
Another problem that has been common has been the lack of ductility in the zinc plate obtained from existing acid zinc bath compositions. Many parts are bent or shaped after plating either through manufacturing processes or through normal use. If the electrodeposit is not reasonably ductile, chipping, flaking and peeling of the plate canoccur, thus causing rejection of the part.
Many of the addition agents prior to this invention have been considerably intolerant to operating temperatures higher than 90 F. These additives would either be chemically destroyed at higher temperatures or just lose their ability to produce bright deposits.
The additionagents and bath compositions of this invention have overcome these serious limitations. With the use of this invention, mugh higher current densities and operating temperatures can be used to obtain lustrous, bright, ductile deposits of zinc from acid zinc plating baths. This is possible because these additives provide bright deposits over a very wide current density range, are'chemically stable, and are not adversely affected by normal increases in temperature.
where R is hydrogen and methyl, and x is about 8 to 20. and polyethylenimine having the formula:
where R is hydrogen, methyl, ethyl, propyl, hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 2- aminoethyl, Z-aminopropyl, and 3-aminopropy1, and y is about 10 to 20.
The present invention is also an addition agent for an acid zinc electroplating bath consisting of from about 1:100 to :1 parts by weight of naphthol polyoxyalkylate and polyethylenimine of the above formulae.
DETAILED DESCRIPTION Both the naphthol polyoxyalkylates and the polyethylenimines of this invention are available in commerce and are supplied as viscous oils and aqueous solutions.
For ease of handling the addition agents were made up as aqueous solutions, but any other suitable solvent or emulsion will work as well.
All testing was done in a conventional 267 ml. Hull Cell using steel cathode panels and a zinc anode. Two ampere panels were run for ten minutes at temperatures ranging from 70 to F. with mechanical agitation.
A general purpose bath was made up which contained 30 gms. ZnCl /liter and 200 gms. NH Cl/liter at a pH of 4.9.
Addition of between 0.1 to 20 gms. of naphthol polyoxyalkylate to the general purpose bath produces only a semi-bright cloudy electrodeposit of zinc from 0 to about 40 amps. per sq. ft. The current density area from 40 amps. per sq. ft. up to 200 amps. per sq. ft. is left as a dark, rough and somewhat spongy electrodeposit.
Similarly, the singular addition of about 0.1 to 20 gms. per liter of polyethylenimine to this bath gives only a semi bright, gray electrodeposit from about 50 amps. per sq. ft. up to 200 amps per sq. ft.
The current density area from 0 to 50 amps per sq. ft. is left as a dark, rough electrodeposit with no trace of brightness.
When the naphthol polyoxyalkylate and the polyethylenimine are added together to this general purpose bath, they act synergistically to provide a bright, lustrous electrodeposit from about 12 amps per sq. ft. to well over 200 amps per sq. ft. In addition to being extremely bright, the deposit is quite ductile. The current densities below 12 amps per sq. ft. can be made bright by the addition of between 0.01 and 10 gms. per liter of a substance selected from the group consisting of anisaldehyde, piperonal, veratraldehyde, benzaldehyde, vanillan, benzylidene acetone, and cinnamic aldehyde.
While the addition agents of this invention are effective in many aqueous, acid zinc plating bath formulations, it is preferred to use any of the basic baths described in the following examples. It will be understood that the following examples are just illustrations and are not meant to limit the use of the invention to thesev bath compositions only;
EXAMPLE I Bath Composition Concentrations in gms/liter Zinc Chloride 30 Ammonium Chloride 200 pH 5.0 Polyethylenimine 4 (600 molecular weight) b-naphthol polyoxyethylene 4 (12 moles of ethylene oxide) EXAMPLE ll Bath Composition Concentration in gms/liter Zinc Sulfate 34 Ammonium Chloride 150 pH 4.8 N-hydroxyethyl polyethylenimine 10 (L200 molecular weight) b-naphthol polyethylene oxide l (15 moles of ethylene oxide) EXAMPLE lII Bath Composition Concentration in gms/liter Zinc chloride 60 Ammonium Chloride 200 pH 5.0
Polyethylenimine 4 (600 molecular weight) b-naphthol polyethylene oxide 4 (8 moles of ethylene oxide) Piperonal (added as methanol 1 solution) EXAMPLE lV Bath Composition Concentration in gms/liter Zinc Chloride 30 Ammonium Chloride 200 pH 6.0 2-hydroxy propyl polyethylenimine 8 (i200 molecular weight) a-naphthol polyethylene oxide moles ethylene oxide) Benzaldehyde (added as methanol 1 I2 moles ethylene oxide) Having thus described this invention in such full,
clear, concise and exact terms as to enable any person skilled in the art to which it pertains to make and use the same, and having set forth the best mode contemplated of carrying out this invention, 1 state that the subject matter which I regard as being my invention is particularly pointed out and distinctly claimed in what is claimed, it being understood that equivalents or modifications of, or substitutions for, parts of the above specifically described embodiment of the invention may be made without departing from the scope of the invention as set forth in what is claimed.
What is claimed is:
1. An addition agent for an acid zinc electroplating bath consisting of from about 1:100 to about parts by weight of naphthol polyoxyalkylate having the formula:
where R is hydrogen, methyl, ethyl propyl, hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 2- aminoethyl, 2-aminopropyl, and 3-aminopropyl, and y is about 10 to about 20.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22959072A | 1972-02-25 | 1972-02-25 | |
| US29682672A | 1972-10-12 | 1972-10-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3767540A true US3767540A (en) | 1973-10-23 |
Family
ID=26923437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00296826A Expired - Lifetime US3767540A (en) | 1972-02-25 | 1972-10-12 | Additive for electrodeposition of bright zinc from aqueous, acid, electroplating baths |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3767540A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928149A (en) * | 1973-09-18 | 1975-12-23 | Max Schloetter Dr Ing | Weak acidic bright ductile zinc electrolyte |
| US4075066A (en) * | 1977-01-27 | 1978-02-21 | R. O. Hull & Company, Inc. | Electroplating zinc, ammonia-free acid zinc plating bath therefor and additive composition therefor |
| US4765871A (en) * | 1981-12-28 | 1988-08-23 | The Boeing Company | Zinc-nickel electroplated article and method for producing the same |
| EP1260614A1 (en) * | 2001-05-24 | 2002-11-27 | Shipley Co. L.L.C. | Tin plating |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2355070A (en) * | 1937-07-03 | 1944-08-08 | Little Inc A | Electrolytic deposition of metal |
| US2384300A (en) * | 1937-07-03 | 1945-09-04 | Little Inc A | Electrolytic deposition of zinc |
| US2853444A (en) * | 1955-10-18 | 1958-09-23 | Dow Chemical Co | Electrowinning of metals |
| US3393135A (en) * | 1965-08-05 | 1968-07-16 | Enthone | Bright zinc electro-plating |
| US3565800A (en) * | 1969-02-04 | 1971-02-23 | Ventron Corp | Ionic compositions containing hg(ii),zn(ii),cd(ii),ag(i),cu(ii),ni(ii) and/or co(ii),and a polymer of an ethylene imine |
-
1972
- 1972-10-12 US US00296826A patent/US3767540A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2355070A (en) * | 1937-07-03 | 1944-08-08 | Little Inc A | Electrolytic deposition of metal |
| US2384300A (en) * | 1937-07-03 | 1945-09-04 | Little Inc A | Electrolytic deposition of zinc |
| US2853444A (en) * | 1955-10-18 | 1958-09-23 | Dow Chemical Co | Electrowinning of metals |
| US3393135A (en) * | 1965-08-05 | 1968-07-16 | Enthone | Bright zinc electro-plating |
| US3565800A (en) * | 1969-02-04 | 1971-02-23 | Ventron Corp | Ionic compositions containing hg(ii),zn(ii),cd(ii),ag(i),cu(ii),ni(ii) and/or co(ii),and a polymer of an ethylene imine |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928149A (en) * | 1973-09-18 | 1975-12-23 | Max Schloetter Dr Ing | Weak acidic bright ductile zinc electrolyte |
| US4075066A (en) * | 1977-01-27 | 1978-02-21 | R. O. Hull & Company, Inc. | Electroplating zinc, ammonia-free acid zinc plating bath therefor and additive composition therefor |
| US4765871A (en) * | 1981-12-28 | 1988-08-23 | The Boeing Company | Zinc-nickel electroplated article and method for producing the same |
| EP1260614A1 (en) * | 2001-05-24 | 2002-11-27 | Shipley Co. L.L.C. | Tin plating |
| US20020187355A1 (en) * | 2001-05-24 | 2002-12-12 | Shipley Company, L.L.C. | Tin plating |
| US6797142B2 (en) | 2001-05-24 | 2004-09-28 | Shipley Company, L.L.C. | Tin plating |
| US20040232000A1 (en) * | 2001-05-24 | 2004-11-25 | Shipley Company, L.L.C. | Tin plating |
| US20060051610A1 (en) * | 2001-05-24 | 2006-03-09 | Shipley Company, L.L.C. | Tin plating |
| US7160629B2 (en) | 2001-05-24 | 2007-01-09 | Shipley Company, L.L.C. | Tin plating |
| KR100885648B1 (en) * | 2001-05-24 | 2009-02-25 | 롬 앤드 하스 일렉트로닉 머트어리얼즈, 엘.엘.씨 | Tin plating |
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