Electrolyte for anodizing magnesium products

Information

  • Patent Application
  • 20070246691
  • Publication Number
    20070246691
  • Date Filed
    February 02, 2007
    17 years ago
  • Date Published
    October 25, 2007
    16 years ago
Abstract
An electrolyte for anodizing magnesium products, includes a base solution, a main blackening agent, an auxiliary blackening agent, and a complexing agent. The base solution includes 2 to 25 g/l of alkali, 1 to 30 g/l of fluoride, and 1 to 35 g/l of silicate. The main blackening agent mainly includes cupric salt, concentration of the cupric salt is from 0.3 to 9 grams per liter (g/l). The auxiliary blackening agent mainly includes oxysalt, concentration of the oxysalt is from 0.1 to 8 g/l. Concentration of the complexing agent is from 0.5 to 20 g/l.
Description
DETAILED DESCRIPTION OF THE INVENTION

An electrolyte used for anodizing magnesium products in accordance with a preferred embodiment of the present invention is provided. A magnesium alloy substrate material as an anode is put in the electrolyte, and another metal (such as stainless steel, or other infusible inert metal) as a cathode is put in the electrolyte. Supplying power between the anode and the cathode until a black coating is formed on the magnesium alloy substrate material by the means of spark discharge. The electrolyte includes a base solution, a main blackening agent, an auxiliary blackening agent, a complexing agent, and an inhibitor. Temperature of the electrolyte is preferably kept between 10 to 60 degrees Celsius (° C.).


The base solution includes alkali, fluoride, silicate, and water. Concentration of the alkali is from 2 to 25 grams per liter (g/l), and preferably from 8 to 12 g/l. Concentration of the fluoride is from 1 to 30 g/l, and preferably from 8 to 12 g/l. Concentration of the silicate is from 1 to 35 g/l, and preferably from 3 to 8 g/l. The alkali includes at least one item selected from the group consisting of potassium hydroxide, and sodium hydroxide. The fluoride includes at least one item selected from the group consisting of potassium fluoride, sodium fluoride, ammonium fluoride, and other compounds including fluorinion. The silicate includes at least one item selected from the group consisting of potassium metasilicate, sodium silicate, potassium fluosilicate, and sodium fluosilicate.


The main blackening agent mainly includes cupric salt. The cupric salt includes at least one item selected from the group consisting of cupric hydroxide, basic copper carbonate, cupric pyrophosphate, cupric citrate, and other metal salts including cupric ions. Concentration of the cupric salt is from 0.3 to 9 g/l, and preferably from 1 to 3 g/l.


The auxiliary blackening agent includes at least one item selected from the group consisting of nickel nitrate, ammonium molybdate, ammonium metavanadate, and other oxysalts. Concentration of the auxiliary blackening agent is from 0.1 to 8 g/l, and preferably from 2 to 4 g/l.


The complexing agent includes at least one item selected from the group consisting of acid and salt of ammonia, ethylenediamine tetracetic acid (EDTA), citric acid, tartaric acid, ethylenediamine, and trolamine. Concentration of the complexing agent is from 0.5 to 20 g/l, and preferably from 3 to 5 g/l.


The inhibitor included in the electrolyte works to increase blackening, and prevent corrosion of the magnesium product. The inhibitor includes at least one item selected from the group consisting of thiourea, sodium m-nitrobenzene sulfonate, and methenamine. Each of the group consisting of thiourea, sodium m-nitrobenzene sulfonate, and methenamine includes amido, hydroxyl, nitryl, or other adsorbing radicals. Concentration of the inhibitor is from 0 to 5 g/l, and preferably from 0.5 to 2 g/l.


The present invention may be explained by means of the following embodiment examples:


EXAMPLE 1

Composition of the electrolyte:


















sodium hydroxide
25 g/l 



sodium silicate
1 g/l



potassium fluoride
10 g/l 



cupric pyrophosphate
4 g/l



nickel nitrate
0.1 g/l  



sodium citrate
8 g/l



thiourea
1 g/l










  • Temperature of the electrolyte is held at 35° C.;

  • Color of the coating formed on the magnesium product: black;

  • Thickness of the coating formed on the magnesium product: 10 micrometers (μm).



EXAMPLE 2

Composition of the electrolyte:


















sodium hydroxide
 13 g/l



sodium silicate
  8 g/l



potassium fluoride
 13 g/l



cupric pyrophosphate
1.8 g/l



nickel nitrate
0.1 g/l



sodium citrate
  5 g/l



thiourea
0.1 g/l










  • Temperature of the electrolyte is held at 25° C.;

  • Color of the coating formed on the magnesium product: black;

  • Thickness of the coating formed on the magnesium product: 14 μm.



EXAMPLE 3

Composition of the electrolyte:


















potassium hydroxide
2 g/l



sodium silicate
35 g/l 



potassium fluoride
1 g/l



cupric pyrophosphate
6 g/l



nickel nitrate
0.1 g/l  



disodium ethylenediamine tetraacetate
3 g/l



methenamine
0.1 g/l  










  • Temperature of the electrolyte is held at 60° C.;

  • Color of the coating formed on the magnesium product: reddish black;

  • Thickness of the coating formed on the magnesium product: 14 μm.



EXAMPLE 4

Composition of the electrolyte:


















sodium hydroxide
15 g/l



sodium silicate
21 g/l



potassium fluoride
10 g/l



cupric hydroxide
0.3 g/l 



ammonium molybdate
 1 g/l



ethylenediamine
0.5 g/l 



thiourea
 1 g/l










  • Temperature of the electrolyte is held at 35° C.;

  • Color of the coating formed on the magnesium product: black;

  • Thickness of the coating formed on the magnesium product: 8 μm.



EXAMPLE 5

Composition of the electrolyte:


















sodium hydroxide
  3 g/l



sodium silicate
  4 g/l



potassium fluoride
 30 g/l



cupric hydroxide
4.5 g/l



ammonium molybdate
0.6 g/l



ethylenediamine
0.5 g/l



sodium citrate
  8 g/l



thiourea
1.5 g/l










  • Temperature of the electrolyte is held at 35° C.;

  • Color of the coating formed on the magnesium product: black;

  • Thickness of the coating formed on the magnesium product: 12 μm.



EXAMPLE 6

Composition of the electrolyte:


















potassium hydroxide
15 g/l 



sodium silicate
21 g/l 



potassium fluoride
10 g/l 



cupric hydroxide
1 g/l



cupric pyrophosphate
8 g/l



ammonium metavanadate
4 g/l



ethylenediamine
5 g/l



sodium citrate
15 g/l 



thiourea
1 g/l










  • Temperature of the electrolyte is held at 35° C.;

  • Color of the coating formed on the magnesium product: bluish black;

  • Thickness of the coating formed on the magnesium product: 18 μm.



EXAMPLE 7

Composition of the electrolyte:


















potassium hydroxide
15 g/l 



sodium silicate
3 g/l



potassium fluoride
15 g/l 



cupric pyrophosphate
1 g/l



ammonium metavanadate
8 g/l



ethylenediamine
2 g/l



potassium sodium tartrate
12 g/l 










  • Temperature of the electrolyte is held at 35° C.;

  • Color of the coating formed on the magnesium product: black;

  • Thickness of the coating formed on the magnesium product: 11 μm.



EXAMPLE 8

Composition of the electrolyte:


















potassium hydroxide
25 g/l 



sodium silicate
11 g/l 



potassium fluoride
10 g/l 



cupric hydroxide
1 g/l



cupric pyrophosphate
2 g/l



ammonium metavanadate
2 g/l



ethylenediamine
1 g/l



sodium citrate
8 g/l



thiourea
1 g/l



Methenamine
4 g/l










  • Temperature of the electrolyte is held at 10° C.;

  • Color of the coating formed on the magnesium product: black;

  • Thickness of the coating formed on the magnesium product: 5 μm.



It is believed that the present embodiments and their advantages will be understood from the foregoing description, and it will be apparent that various changes may be made thereto without departing from the spirit and scope of the invention or sacrificing all of its material advantages, the examples hereinbefore described merely being preferred or exemplary embodiments of the invention.

Claims
  • 1. An electrolyte for anodizing magnesium products, the electrolyte comprising: a base solution;a main blackening agent mainly comprising cupric salt, concentration of the cupric salt ranging from 0.3 to 9 grams per liter (g/l);an auxiliary blackening agent mainly comprising oxysalt, concentration of the oxysalt ranging from 0.1 to 8 grams per liter (g/l); anda complexing agent, concentration of the complexing agent ranging from 0.5 to 20 g/l.
  • 2. The electrolyte as claimed in claim 1, wherein the base solution comprises 2 to 25 g/l of alkali, 1 to 30 g/l of fluoride, and 1 to 35 g/l of silicate.
  • 3. The electrolyte as claimed in claim 2, wherein concentration of the alkali is from 8 to 12 g/l, the fluoride from 8 to 12 g/l, and the silicate from 3 to 8 g/l.
  • 4. The electrolyte as claimed in claim 2, wherein the alkali comprises at least one item selected from the group consisting of potassium hydroxide, and sodium hydroxide.
  • 5. The electrolyte as claimed in claim 2, wherein the fluoride comprises at least one item selected from the group consisting of potassium fluoride, sodium fluoride, and ammonium fluoride.
  • 6. The electrolyte as claimed in claim 2, wherein the silicate comprises at least one item selected from the group consisting of potassium metasilicate, sodium silicate, potassium fluosilicate, and sodium fluosilicate.
  • 7. The electrolyte as claimed in claim 1, wherein the cupric salt comprises at least one item selected from the group consisting of cupric hydroxide, basic copper carbonate, cupric pyrophosphate, and cupric citrate.
  • 8. The electrolyte as claimed in claim 1, wherein the oxysalt comprises at least one item selected from the group consisting of nickel nitrate, ammonium molybdate, and ammonium metavanadate.
  • 9. The electrolyte as claimed in claim 1, wherein the complexing agent comprises at least one item selected from the group consisting of acid and salt of ammonia, ethylenediamine tetracetic acid (EDTA), citric acid, tartaric acid, ethylenediamine, and trolamine.
  • 10. The electrolyte as claimed in claim 1, further comprising an inhibitor for increase of blackening and preventing corrosion of the magnesium products, wherein the inhibitor comprises at least one item selected from the group consisting of thiourea, sodium m-nitrobenzene sulfonate, and methenamine, each of the thiourea, sodium m-nitrobenzene sulfonate, and methenamine including amido, hydroxyl, or nitryl absorbing radicals, concentration of the inhibitor is from 0 to 5 g/l.
  • 11. The electrolyte as claimed in claim 10, wherein concentration of the inhibitor is from 0.5 to 2 g/l.
  • 12. The electrolyte as claimed in claim 1, wherein concentration of the cupric salt is from 1 to 3 g/l, the oxysalt from 2 to 4 g/l, and the complexing agent from 3 to 5 g/l.
  • 13. An electrolyte for anodizing a magnesium product, the electrolyte comprising: a base solution comprising 8 to 12 g/l of alkali, 8 to 12 g/l of fluoride, and 3 to 8 g/l of silicate;a main blackening agent mainly comprising 1 to 3 g/l of cupric salt;an auxiliary blackening agent mainly comprising 2 to 4 g/l of oxysalt; anda complexing agent, concentration of the complexing agent ranging from 3 to 5 g/l.
  • 14. The electrolyte as claimed in claim 13, further comprising an inhibitor, wherein the alkali is sodium hydroxide concentration of which is 13 grams per liter (g/l), the fluoride is potassium fluoride concentration of which is 13 g/l, the silicate is sodium silicate concentration of which is 8 g/l, the cupric salt is cupric pyrophosphate concentration of which is 1.8 g/l, the oxysalt is nickel nitrate concentration of which is 0.1 g/l, the complexing agent is sodium citrate concentration of which is 5 g/l, and the inhibitor is thiourea concentration of which is 0.1 g/l.
  • 15. The electrolyte as claimed in claim 13, further comprising an inhibitor, wherein the alkali is potassium hydroxide concentration of which is 2 grams per liter (g/l), the fluoride is potassium fluoride concentration of which is 1 g/l, the silicate is sodium silicate concentration of which is 35 g/l, the cupric salt is cupric pyrophosphate concentration of which is 6 g/l, the oxysalt is nickel nitrate concentration of which is 0.1 g/l, the complexing agent is disodium ethylenediamine tetraacetate concentration of which is 3 g/l, and the inhibitor is methenamine concentration of which is 0.1 g/l.
  • 16. The electrolyte as claimed in claim 13, further comprising an inhibitor, wherein the alkali is sodium hydroxide concentration of which is 3 grams per liter (g/l), the fluoride is potassium fluoride concentration of which is 30 g/l, the silicate is sodium silicate concentration of which is 4 g/l, the main blackening agent is cupric hydroxide concentration of which is 4.5 g/l, the oxysalt is ammonium molybdate concentration of which is 0.6 g/l, the complexing agent is ethylenediamine and sodium citrate concentrations of which are 0.5 g/l and 8 g/l respectively, and the inhibitor is thiourea concentration of which is 1.5 g/l.
  • 17. The electrolyte as claimed in claim 13, wherein the alkali is potassium hydroxide concentration of which is 15 grams per liter (g/l), the fluoride is potassium fluoride concentration of which is 15 g/l, the silicate is sodium silicate concentration of which is 3 g/l, the cupric salt is cupric pyrophosphate concentration of which is 1 g/l, the oxysalt is ammonium metavanadate concentration of which is 8 g/l, and the complexing agent is ethylenediamine and potassium sodium tartrate concentrations of which are 2 g/l and 12 g/l respectively.
  • 18. The electrolyte as claimed in claim 13, wherein the complexing agent comprises at least one item selected from the group consisting of acid and salt of ammonia, ethylenediamine tetracetic acid (EDTA), citric acid, tartaric acid, ethylenediamine, and trolamine.
  • 19. The electrolyte as claimed in claim 13, further comprising an inhibitor for increase of blackening and preventing corrosion of the substrate material, wherein the inhibitor comprises at least one item selected from the group consisting of thiourea, sodium m-nitrobenzene sulfonate, and methenamine, each of the thiourea, sodium m-nitrobenzene sulfonate, and methenamine including amido, hydroxyl, or nitryl absorbing radicals.
  • 20. An electrolyte for anodizing magnesium products, comprising: a base solution comprising 2 to 25 g/l (grams per liter ) of alkalim, 1 to 30 g/l of fluoride, and 1 to 35 g/l of silicate;a main blackening agent comprising 0.3 to 9 g/l of cupric salt;an auxiliary blackening agent comprising 0.1 to 8 g/l of oxysalt;a complexing agent concentration of which ranges from 0.5 to 20 g/l, the complexing agent comprising at least one item selected from the group consisting of acid of ammonia, ethylenediamine tetracetic acid (EDTA), citric acid, tartaric acid, ethylenediamine, and trolamine, and salt of ammonia, ethylenediamine tetracetic acid (EDTA), citric acid, tartaric acid, ethylenediamine, and trolamine; andan inhibitor comprising at least one item selected from the group consisting of thiourea, sodium m-nitrobenzene sulfonate, and methenamine each of which comprises at least one of amido, hydroxyl and nitryl absorbing radicals, concentration of the inhibitor ranging from 0 to 5 g/l.
Priority Claims (1)
Number Date Country Kind
200610060396.4 Apr 2006 CN national
CROSS-REFERENCES TO RELATED APPLICATION

Relevant subject matter is disclosed in the co-pending U.S. patent application (Attorney Docket No. US10093) filed on the same date and entitled “METHOD FOR ANODIZING MAGNESIUM PRODUCTS”, which is assigned to the same assignee with this patent application.