Silver-electroplating process

Claim 2

A process for silver-plating which comprises the steps of preplating a substrate material in an aqueous preplating solution comprising 10 -5 to 0.02 mole/l of silver and more than 0.01 mole/l of a silver complexing agent under non-current density, to preplate a sufficient thickness of silver to restrain or substantially prevent substitution plating, and then electroplating the preplated substrate material by supplying an electric current to said material in an aqueous silver plating solution comprising silver and thiocyanic ions and having a pH in a range of from 0.5 to 10.5.

Claim 3

A process according to claim 1, wherein the silver is in the electroplating aqueous silver plating solution in a concentration of 0.04 to 0.8 mole/l.

Claim 4

A process according to claim 2, wherein the electroplating aqueous silver plating solution is made by dissolving AgCl, AgBr, AgI, AgSCN, Ag 2 O, Ag 2 CO 3 , Ag 2 SO 4 , AgNO 3 , AgSCN, Ag 2 SeO 4 , or AgCH 3 COO 3 in an aqueous medium.

Claim 5

A process according to claim 1, wherein the thiocyanic ions are in the electroplating aqueous silver plating solution in a concentration of 0.5 to 10 moles/l.

Claim 6

A process according to claim 4, wherein the thiocyanic ions are generated from dissolved KSCN, NaSCN, NH 4 SCN, CsSCN, or RbSCN.

Claim 7

A process according to claim 1, wheren the electroplating aqueous silver plating solution contains a film-improving agent in an amount sufficient to suppress a local growth of silver deposition.

Claim 8

A process according to claim 6, wherein the film-improving agent is at least one member selected from the group consisting of: ______________________________________ Bromine ions (Br.sup.-) 1 × 10.sup.-3 to 0.1 mole/l Iodine ions (I.sup.-) 1.2 × 10.sup.-4 to 1.2 × 10.sup.-3 mole/l Selenocyanic ions (SeCN.sup.-) 5 × 10.sup.-4 to 1 × 10.sup.-2 mole/l Cobalt ions (Co.sup.++) 5 × 10.sup.-6 to 5 × 10.sup.-3 mole/l Stannic acid ions (SnO.sub.3.sup.--) 1 × 10.sup.-4 to 1 × 10.sup.-2 mole/l Thiourea (SC(NH.sub.2).sub.2) 5 × 10.sup.-6 5 × 10.sup.-3 mole/l Triethanol amine ((HOCH.sub.2 CH.sub.2).sub.3 N) 1 × 10.sup.-3 to 1 mole/l Silinic acid ions (SeO.sub.4.sup.--) 5 × 10.sup.-6 to 5 × 10.sup.-3 ______________________________________ mole/l

Claim 9

A process according to claim 7, wherein the bromine ions are generated from dissolved AgBr, KBr, or NaBr.

Claim 10

A process according to claim 7, wherein the iodine ions are generated from dissolved KI, NaI, AgI, RbI, or CsI.

Claim 11

A process according to claim 7, wherein the selenocyanic ions are generated from dissolved H 2 SeO 4 , Ag 2 SeO 4 , K 2 SeO 4 or Na 2 SeO 4 .

Claim 12

A process according to claim 7, wherein the selenic acid ions are generated from dissolved H 2 SeO 4 , Ag 2 SeO 4 , K 2 SeO 4 or Na 2 SeO 4 .

Claim 13

A process according to claim 7, wherein the cobalt ions are generated from dissolved CoSO 4 , CoCl 2 or CoSeO 4 .

Claim 14

A process according to claim 7, wherein the stannic acid ions (SnO 3 -- ) are generated from dissolved Na 2 SnO 3 .

Claim 15

A process according to claim 1, wherein the substrate material is copper, nickel or their alloys.

Claim 16

A process according to claim 1, wherein the silver complexing agent has a stability constant of 1×10 6 to 1×10 15 at 25° C. with relation to silver in the aqueous preplating solution.

Claim 17

A process according to claim 1, wherein the silver complexing agent is selected from the group consisting of thiocyanic ions, ammonia, thiosulfate ions, bromine ions, iodine ions, methylamine, thiourea, dimethylamine, ethylamine, ethyleneamine, glycine, 2-hydroxy ethyleneamine, imidazole, allylamine, n-propylamine, 2,2'-diamino diethylamine, 2,2'-diamino diethylsulfide, histidine, phenylthioacetic acid, benzylthioacetic acid and β-benzylthiopropionic acid.

Claim 18

A process according to claim 1, wherein the preplating is carried out for a period of about 10 seconds to about 30 minutes.

Claim 19

A process according to claim 1, wherein the deposition speed of silver during the preplating is within 0.001 mg/dm 2 to 0.01 mg/dm 2 per second.