US2018171499A1PendingUtilityA1
Method of obtaining a yellow gold alloy deposition by galvanoplasty without using toxic materials
Assignee: SWATCH GROUP RES & DEV LTDPriority: Oct 15, 2009Filed: Feb 16, 2018Published: Jun 21, 2018
Est. expiryOct 15, 2029(~3.2 yrs left)· nominal 20-yr term from priority
B05D 1/18C25D 3/62C25D 3/56C25D 3/58C25D 7/005
68
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Claims
Abstract
A method of galvanoplastic deposition of a gold alloy on an electrode dipped into a bath including metal gold in alkaline aurocyanide form, organometallic compounds, a wetting agent, a sequestering agent and free cyanide, where the alloy metals are copper, in double copper and potassium cyanide form, and silver in cyanide form, allowing a mirror bright yellow gold alloy to be deposited on the electrode.
Claims
exact text as granted — not AI-modified1 . A method for the galvanoplastic deposition of a gold alloy on an electrode, the method comprising:
(a) dipping an electrode into a bath, wherein the hath comprises:
gold metal in alkaline aurocyanide form,
copper metal in copper and double potassium cyanide form,
silver metal in cyanide form,
organometallic compounds,
a wetting agent,
a sequestering agent, and
free cyanide,
wherein the bath has a proportion of 9.08% gold, 90.85% copper, and 0.07% silver, and the bath does not comprise cadmium or zinc; and then,
(b) galvanoplastically depositing a bright 3N colour gold alloy made of 75% gold, 21% copper, and 4% silver on the electrode, wherein the gold alloy has a thickness of 200 to 800 μm.
2 . The method according to claim 1 , wherein the bath comprises 5.5 g.l −1 of gold metal in alkaline aurocyanide form, 55 g.l −1 of copper metal in copper and double alkaline cyanide form, and 40 mg.l −1 of silver metal in cyanide form.
3 . The method according to claim 2 , wherein the bath comprises from 13 to 35 g.l −1 of cyanide.
4 . The method according to claim 1 , wherein a concentration of the wetting agent is between 0.05 and 10 ml.l −1 .
5 . The method according to claim 1 , wherein the wetting agent is selected from the group consisting of poly-oxy-alkenic, ether phosphate, lauryl sulphate, dimethyldodecylamine-N-oxide, and a dimethyl(dodecyl) ammonium propane sulfonate.
6 . The method according to claim 1 , wherein the bath further comprises an amine, and wherein a concentration of the amine is between 0.01 and 5 ml.l −1 .
7 . The method according to claim 1 , wherein the bath further comprises a depolariser, and wherein a concentration of the depolariser is between 0.1 mg.l −1 to 20 mg.l −1 .
8 . The method according to claim 1 , wherein the bath further comprises at least one conductive salt selected from the group consisting of a phosphate, a carbonate, a citrate, a sulphate, a tartrate, a gluconate, and a phosphonate conductive salt.
9 . The method according to claim 1 , wherein the temperature of the hath is kept between 50 and 80° C.
10 . The method according to claim 1 , wherein the pH of the bath is kept between 8 and 12.
11 . The method according to claim 1 , wherein the galvanoplastically depositing (b) is performed at a current density of between 0.3 A dm −2 .
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