US2003172998A1PendingUtilityA1
Composition and process for the treatment of metal surfaces
Priority: Mar 14, 2002Filed: Mar 14, 2002Published: Sep 18, 2003
Est. expiryMar 14, 2022(expired)· nominal 20-yr term from priority
C23C 22/40C23C 22/44
39
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Claims
Abstract
A method of forming a conversion layer on a metallic surface and a composition usable in the method are provided. The composition is an aqueous solution comprising a source of tungstate ions and a soluble material comprising zirconium. The method provides a conversion coating on a surface that can then be painted or otherwise treated. The conversion coatings of the present invention are minimally affected by heating and/or baking, unlike chromate conversion coatings of the prior art.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of forming a conversion layer on a metallic surface comprising the steps of:
treating the metallic surface with an aqueous treating solution comprising:
(a) a source of tungstate ions; and
(b) a soluble material comprising zirconium; and
thereafter drying and/or baking the treated metal surface.
2 . A method according to claim 1 , wherein the aqueous treating solution further comprises ammonium hydroxide.
3 . A method according to claim 1 , wherein the source of tungstate ions is selected from the group consisting of ortho-tungstates, meta-tungstates and para-tungstates, polytungstates, heteropolytungstates, isopolytungstates, peroxytungstates, and combinations thereof.
4 . A method according to claim 3 , wherein the source of tungstate ions is meta-tunstate or para-tungstate.
5 . A method according to claim 3 , wherein the source of tungstate ions is selected from the group consisting of sodium, potassium, lithium, calcium, cerium, barium, magnesium, strontium, hydrogen and ammonium tungstate salts.
6 . A method according to claim 3 , wherein the source of tungstate ions is tangstic acid, hexaamonium salt.
7 . A method according to claim 1 , wherein the concentration of tungstate ions, measured as tungsten, in treating solution is about 0.01 g/l to about 10.0 g/l.
8 . A method according to claim 7 , wherein the concentration of tungstate ions, measured as tungsten, in the treating solution is about 0.1 g/l to about 1.5 g/l.
9 . A method according to claim 8 , wherein the concentration of tungstate ions, measured as tungsten, in the treating solution is 1.0 g/l.
10 . A method according to claim 1 , wherein the soluble material comprising zirconium is selected from the group consisting of zirconium ammonium fluoride, dihydrogen hexafluorozirconate, potassium hexafluorozirconate, zirconium sulfate, zirconium carbonate, zirconium nitrate, and zirconium phosphate.
11 . A method according to claim 10 , wherein the soluble material comprising zirconium is dihydrogen hexafluorozirconate.
12 . A method according to claim 1 , wherein the concentration of the soluble material comprising zirconium in the treating solution is about 0.01 g/l to about 2.0 g/l.
13 . A method according to claim 12 , wherein the concentration of the soluble material comprising zirconium in the treating solution is about 0.05 g/l to about 0.5 g/l.
14 . A method according to claim 1 , wherein the aqueous treating solution further comprises a soluble aluminum salt.
15 . A method according to claim 14 , wherein the concentration of the soluble aluminum salt is between 5 and 500 parts per million as aluminum.
16 . A method according to claim 1 , wherein the temperature of the treating solution is within the range of about 55° F. to about 180° F.
17 . A method according to claim 16 , wherein the temperature of the treating solution is about 70° F. to about 120° F.
18 . A method according to claim 1 , wherein the pH of the treating solution is maintained from about 2.8 to about 7.0.
19 . A method according to claim 1 , wherein the parts are cleaned prior to treating the metallic surface with the treating solution.
20 . A method according to claim 19 , wherein the metallic surface is deoxidized after cleaning and prior to treating with the treating solution.
21 . A method according to claim 1 , wherein the treating solution is free of chromium.
22 . A method according to claim 1 , wherein the treating solution is applied by immersion or by spraying.
23 . A method according to claim 1 , wherein the treating solution further comprises at least one of a surfactant, an accelerator, a dye, an organic polymer, a buffering agent, and a pH adjusting agent.
24 . An aqueous conversion coating composition comprising a source of tungstate ions and a soluble material comprising zirconium.
25 . A composition according to claim 24 , wherein the aqueous treating solution further comprises ammonium hydroxide.
26 . A composition according to claim 24 , wherein the source of tungstate ions is selected from the group consisting of ortho-tungstates, meta-tungstates and para-tungstates, polytungstates, heteropolytungstates, isopolytungstates, peroxytungstates, and combinations thereof.
27 . A composition according to claim 26 , wherein the source of tungstate ions is meta-tungstate or para-tungstate.
28 . A composition according to claim 26 , wherein the source of tungstate ions is selected from the group consisting of sodium, potassium, lithium, calcium, cerium, barium, magnesium, strontium, hydrogen and ammonium tungstate salts.
29 . A composition according to claim 26 , wherein the source of tungstate ions is tungstic acid, hexaamonium salt.
30 . A composition according to claim 24 , wherein the concentration of tungstate ions, measured as tungsten, in treating solution is about 0.01 g/l to about 10.0 g/l.
31 . A composition according to claim 30 , wherein the concentration of tungstate ions, measured as tungsten, in the treating solution is about 0.1 g/l to about 1.5 g/l.
32 . A composition according to claim 31 , wherein the concentration of tungstate ions, measured as tungsten, in the treating solution is 1.0 g/l.
33 . A composition according to claim 24 , wherein the soluble material comprising zirconium is selected from the group consisting of zirconium ammonium fluoride, dihydrogen hexafluorozirconate, potassium hexafluorozirconate, zirconium sulfate, zirconium carbonate, zirconium nitrate, and zirconium phosphate.
34 . A composition according to claim 33 , wherein the soluble material comprising zirconium is dihydrogen hexafluorozirconate.
35 . A composition according to claim 24 , wherein the concentration of the soluble material comprising zirconium in the treating solution is about 0.01 g/l to about 2.0 g/l.
36 . A composition according to claim 35 , wherein the concentration of the soluble material comprising zirconium in the treating solution is about 0.05 g/l to about 0.5 g/l.
37 . A composition according to claim 24 , wherein the aqueous treating solution further comprises a soluble aluminum salt.
38 . A composition according to claim 37 , wherein the concentration of the soluble aluminum salt is between 5 and 500 parts per million as aluminum.
39 . A composition according to claim 24 , wherein the temperature of the treating solution is within the range of about 55° F. to about 180° F.
40 . A composition according to claim 39 , wherein the temperature of the treating solution is about 70° F. to about 120° F.
41 . A composition according to claim 24 , wherein the pH of the treating solution is maintained from about 2.8 to about 7.0.
42 . A composition according to claim 24 , wherein the treating solution is free of chromium.
43 . A composition according to claim 24 , wherein the treating solution further comprises at least one of a surfactant, an accelerator, a dye, an organic polymer, a buffering agent, and a pH adjusting agent.Join the waitlist — get patent alerts
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