US3682789A - Electrolytic solution for zinc plating - Google Patents
Electrolytic solution for zinc plating Download PDFInfo
- Publication number
- US3682789A US3682789A US795071*A US3682789DA US3682789A US 3682789 A US3682789 A US 3682789A US 3682789D A US3682789D A US 3682789DA US 3682789 A US3682789 A US 3682789A
- Authority
- US
- United States
- Prior art keywords
- zinc
- electrolytic solution
- zinc plating
- chloride
- solution
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/22—Electroplating: Baths therefor from solutions of zinc
Definitions
- This invention relates to an electrolytic solution for zinc plating. More particularly, it relates to a process for plating zinc on metal surfaces and an electrolytic solution therefor which contains (1) zinc acetate, zinc chloride or zinc sulfate; (2) ammonium chloride; 3) sodium or potassium gluconate, (4) boric acid and (5) glossing agents.
- Acidic zinc sulfate electrolytic solutions, alkaline zinc cyanide electrolytic solutions, etc. have principally been used heretofore as electrolytic solutions for galvanic zinc plating.
- the alkaline zinc cyanide electrolytic solutions are considerably superior to the acidic zinc sulfate electrolytic solutions insofar as uniform depositability is concerned.
- alkaline zinc cyanide electrolytic solutions have usually been used.
- the alkaline zinc cyanide electrolytic solutions contain very toxic cyanides, making the disposition of the electrolytic solution a very troublesome matter. Furthermore, much expense and valuable space are required for the disposal of the waste solution.
- One of the objects of the present invention is to provide an electrolytic solution which contains no toxic cyanides and is equal or superior in performance and effect to an alkaline zinc cyanide electrolytic solution.
- Another object of the invention is to provide an electrolytic solution capable of giving an excellent corrosion resistance by means of a relatively simple operation and device.
- a further object of the invention is to provide an electrolytic solution capable of producing a good glossy and smooth surface.
- a still further object of the present invention is to provide an eflicacious and advantageous process for the plating of zinc.
- the objectives outlined above are attained by using for the zinc plating an electrolytic solution comprising (1) zinc acetate, zinc chloride or zinc sulfate, (2) ammonium chloride, (3) sodium or potassium gluconate, (4) boric acid and (5) glossing agents.
- the zinc ion concentration employed in the electrolytic solution of the present invention is 10-100 g./l. (grams per liter), preferably 20-50 g./l.
- the amount of zinc ion is closely related to the uniform depositability and cathode current efficiency which can be obtained, and when the zinc ion is used in excess, the uniformity of the deposit tends to worsen and become undesirable.
- the zinc salts used in the present invention are zinc acetate, zinc chloride and zinc sulfate.
- the ammonium chloride concentration used in the electrolytic solution is preferably 30-150 g./l.
- the ammonium chloride is used as a current-passing assistant, and when the ammonium chloride is used in excess amounts, the deposited zinc surface tends to become worse, with the result that the corrosion resistance also tends to deteriorate in quality.
- the adhesiveness of the deposited zinc to metal surface tends to become poor when too much or too little of an amount of ammonium chloride is used.
- the concentration of potassium or sodium gluconate used in the electrolytic solution is preferably 30-300 g./l. More specifically, the concentration of sodium or potassium gluconate is preferably 180-220 g./l. in the case of zinc acetate, -120 g./l. in the case of zinc chloride and -140 g./l. in the case of zinc sulfate.
- the addition of sodium or potassium gluconate to the solution makes it possible to obtain a deposited zinc surface having a uniform gloss distribution. A film of chromate having a good corrosion resistance can be readily formed on the deposited zinc surface by chromate treatment. The adhesiveness of the deposited zinc to metal surface tends to become worse when too small of a quantity of gluconate is used.
- the boric acid concentration is preferably 10-100 g./l. more preferably 15-25 g./l.
- the boric acid acts as a pH buffering agent. By adding H BO to the electrolytic solution, the gloss of the deposited zinc can be much improved.
- the pH of the solution is preferably kept at 2 to 7, more preferably 4-5.
- the pH is closely related to the adhesiveness of deposited zinc to metal plate. The adhesiveness tends to become poor when too high or too low of a pH is used. A too low pH increases the solution of the zinc anode, and control of the electrolytic solution becomes difiicult.
- Glossing agents which may be employed in the solution include, for example, gelatin, glue, dextrin, polyethylene glycol and triethanolamine.
- aqueous solution further contains an effective amount of at least one glossing agent selected from the group consisting of gelatin, glue, dextrin, polyethylene glycol and triethanolamine.
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP497668 | 1968-01-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3682789A true US3682789A (en) | 1972-08-08 |
Family
ID=11598611
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US795071*A Expired - Lifetime US3682789A (en) | 1968-01-29 | 1969-01-29 | Electrolytic solution for zinc plating |
Country Status (6)
Country | Link |
---|---|
US (1) | US3682789A (xx) |
BE (1) | BE727608A (xx) |
CH (1) | CH508732A (xx) |
DE (1) | DE1904319B2 (xx) |
FR (1) | FR2000932A1 (xx) |
GB (1) | GB1201587A (xx) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4016013A (en) * | 1974-02-07 | 1977-04-05 | Ciba-Geigy Corporation | Process for producing diffusion layers of carbides, nitrides and/or carbonitrides |
CN107142501A (zh) * | 2017-07-12 | 2017-09-08 | 合肥信亚达智能科技有限公司 | 一种环保镀锌液及其制备方法 |
US9899695B2 (en) | 2015-05-22 | 2018-02-20 | General Electric Company | Zinc-based electrolyte compositions, and related electrochemical processes and articles |
-
1969
- 1969-01-28 CH CH124269A patent/CH508732A/de not_active IP Right Cessation
- 1969-01-29 US US795071*A patent/US3682789A/en not_active Expired - Lifetime
- 1969-01-29 DE DE19691904319 patent/DE1904319B2/de active Pending
- 1969-01-29 GB GB5021/69A patent/GB1201587A/en not_active Expired
- 1969-01-29 FR FR6901831A patent/FR2000932A1/fr not_active Withdrawn
- 1969-01-29 BE BE727608D patent/BE727608A/xx unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4016013A (en) * | 1974-02-07 | 1977-04-05 | Ciba-Geigy Corporation | Process for producing diffusion layers of carbides, nitrides and/or carbonitrides |
US9899695B2 (en) | 2015-05-22 | 2018-02-20 | General Electric Company | Zinc-based electrolyte compositions, and related electrochemical processes and articles |
CN107142501A (zh) * | 2017-07-12 | 2017-09-08 | 合肥信亚达智能科技有限公司 | 一种环保镀锌液及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
GB1201587A (en) | 1970-08-12 |
BE727608A (xx) | 1969-07-01 |
FR2000932A1 (xx) | 1969-09-19 |
DE1904319A1 (de) | 1969-09-25 |
DE1904319B2 (de) | 1971-04-22 |
CH508732A (de) | 1971-06-15 |
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