US2004140221A1PendingUtilityA1
Method of anodizing aluminum utilizing stabilized silicate solutions
Priority: Jan 21, 2003Filed: Jan 21, 2003Published: Jul 22, 2004
Est. expiryJan 21, 2023(expired)· nominal 20-yr term from priority
C25D 11/08C25D 11/10
51
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Claims
Abstract
An anodizing solution, and method of anodizing, comprising suspending at least one aluminium substrate in an anodizing solution and applying an anodizing current to the anodizing solution. The anodizing solution comprises 0.01-5%, by weight, sodium silicate and 0.01-5%, by weight, α-amino acid.
Claims
exact text as granted — not AI-modifiedClaimed is:
1 . An electrolyte composition comprising 0.01-5%, by weight, sodium silicate and 0.01-5%, by weight, α-amino acid.
2 . The electrolyte composition of claim 1 comprising 0.1% and 1%, by weight, sodium silicate.
3 . The electrolyte composition of claim 1 comprising 0.1% and 1%, by weight, α-amino acid.
4 . The electrolyte composition of claim 1 wherein said α-amino acid comprises at least one compound selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine, threonine, glycine, alanine, valine, leucine, isoleucine, methionine, proline, phenylalanine, tryptothan, serine, cysteine, asparginine, glutamine, arginine, histidine, and α-aminoadipic acid.
5 . The electrolyte composition of claim 4 wherein said α-amino acid is selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine and threonine.
6 . The electrolyte composition of claim 5 wherein said α-amino acid is selected from a group consisting of aspartic acid and glutamic acid.
7 . The electrolytic composition of claim 6 wherein said α-amino acid is aspartic acid.
8 . The electrolyte composition of claim 1 wherein said α-amino acid has a solubility of at least 0.04 g/100 ml H 2 O at 25° C.
9 . The electrolyte composition of claim 1 wherein said composition has a pH of at least about 6 to no more than about 7.
10 . The electrolyte composition of claim 1 further comprising an α-hydroxy carboxylic acid.
11 . The electrolyte composition of claim 10 wherein said α-hydroxy carboxylic acid is present at a concentration of no more than about 5%, by weight.
12 . The electrolyte composition of claim 10 wherein said α-hydroxy carboxylic acid is selected from a group consisting of malic acid, tartartic acid and citric acid.
13 . The electrolyte composition of claim 12 wherein said α-hydroxy carboxylic acid is tartartic acid.
14 . A method of anodizing comprising suspending at least one aluminium substrate into an electrolytic solution and applying an anodizing current to the electrolytic solution wherein the electrolyte solution comprises 0.01-5%, by weight, sodium silicate and 0.01-5%, by weight, α-amino acid.
15 . The method of anodizing of claim 14 comprising 0.1% and 1%, by weight, sodium silicate.
16 . The method of anodizing of claim 14 comprising 0.1% and 1%, by weight, α-amino acid.
17 . The method of anodizing of claim 14 wherein said α-amino acid comprises at least one compound selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine, threonine, glycine, alanine, valine, leucine, isoleucine, methionine, proline, phenylalanine, tryptothan, serine, cysteine, asparginine, glutamine, arginine, histidine, and α-aminoadipic acid.
18 . The method of anodizing of claim 17 wherein said α-amino acid is selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine and threonine.
19 . The method of anodizing of claim 18 wherein said α-amino acid is selected from a group consisting of aspartic acid and glutamic acid.
20 . The method of anodizing of claim 19 wherein said α-amino acid is aspartic acid.
21 . The method of anodizing of claim 14 wherein said α-amino acid has a solubility of at least 0.04 g/100 ml H 2 O at 25° C.
22 . The method of anodizing of claim 14 wherein said composition has a pH of at least about 6 to no more than about 7.
23 . The method of anodizing of claim 14 further comprising an α-hydroxy carboxylic acid.
24 . The method of anodizing of claim 23 wherein said α-hydroxy carboxylic acid is present at a concentration of no more than about 5%, by weight.
25 . The method of anodizing of claim 23 wherein said α-hydroxy carboxylic acid is selected from a group consisting of malic acid, tartartic acid and citric acid.
26 . The method of anodizing of claim 25 wherein said α-hydroxy carboxylic acid is tartartic acid.
27 . A method for forming an aluminium oxide barrier layer on an aluminium substrate comprising suspending at least one aluminium substrate into an electrolytic solution and applying an anodizing current to the electrolytic solution wherein the electrolyte solution comprises 0.01-5%, by weight, sodium silicate and 0.01-5%, by weight, α-amino acid.
28 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 wherein said aluminium oxide barrier layer comprises silicate.
29 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 28 wherein said aluminium oxide barrier layer comprises about 20 ppm to about 100 ppm silicate.
30 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 29 wherein said aluminium oxide barrier layer comprises about 50 to about 100 ppm silicate.
31 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 30 wherein said aluminium oxide barrier layer comprises about 60 ppm silicate.
32 . A capacitor comprising an aluminium substrate anodized by the method of claim 27 .
33 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 comprising 0.1% and 1%, by weight, sodium silicate.
34 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 comprising 0.1% and 1%, by weight, α-amino acid.
35 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 wherein said α-amino acid comprises at least one compound selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine, threonine, glycine, alanine, valine, leucine, isoleucine, methionine, proline, phenylalanine, tryptothan, serine, cysteine, asparginine, glutamine, arginine, histidine, and α-aminoadipic acid.
36 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 35 wherein said α-amino acid is selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine and threonine.
37 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 36 wherein said α-amino acid is selected from a group consisting of aspartic acid and glutamic acid.
38 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 37 wherein said α-amino acid is aspartic acid.
39 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 wherein said α-amino acid has a solubility of at least 0.04 g/100 ml H 2 O at 25° C.
40 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 wherein said composition has a pH of at least about 6 to no more than about 7.
41 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 27 further comprising an α-hydroxy carboxylic acid.
42 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 41 wherein said α-hydroxy carboxylic acid is present at a concentration of no more than about 5%, by weight.
43 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 41 wherein said α-hydroxy carboxylic acid is selected from a group consisting of malic acid, tartartic acid and citric acid.
44 . The method for forming an aluminium oxide barrier layer on an aluminium substrate of claim 43 wherein said α-hydroxy carboxylic acid is tartartic acid.
45 . An aluminium substrate comprising an aluminium oxide barrier layer prepared by a method comprising suspending said aluminium substrate into an electrolytic solution and applying an anodizing current to the electrolytic solution wherein the electrolyte solution comprises 0.01-5%, by weight, sodium silicate and 0.01-5%, by weight, α-amino acid.
46 . The aluminium substrate of claim 45 wherein said aluminium oxide barrier layer comprises silicate.
47 . The aluminium substrate of claim 45 wherein said aluminium oxide barrier layer comprises about 20 ppm to about 100 ppm silicate.
48 . The aluminium substrate of claim 47 wherein said aluminium oxide barrier layer comprises about 50 to about 100 ppm silicate.
49 . The aluminium substrate of claim 48 wherein said aluminium oxide barrier layer comprises about 60 ppm silicate.
50 . A capacitor comprising an aluminium substrate anodized by the method of claim 45 .
51 . The aluminium substrate of claim 45 comprising 0.1% and 1%, by weight, sodium silicate.
52 . The aluminium substrate of claim 45 comprising 0.1% and 1%, by weight, α-amino acid.
53 . The aluminium substrate of claim 45 wherein said α-amino acid comprises at least one compound selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine, threonine, glycine, alanine, valine, leucine, isoleucine, methionine, proline, phenylalanine, tryptothan, serine, cysteine, asparginine, glutamine, arginine, histidine, and α-aminoadipic acid.
54 . The aluminium substrate of claim 53 wherein said α-amino acid is selected from a group consisting of aspartic acid, glutamic acid, lysine, tyrosine and threonine.
55 . The aluminium substrate of claim 54 wherein said α-amino acid is selected from a group consisting of aspartic acid and glutamic acid.
56 . The aluminium substrate of claim 55 wherein said α-amino acid is aspartic acid.
57 . The aluminium substrate of claim 45 wherein said α-amino acid has a solubility of at least 0.04 g/100 ml H 2 O at 25° C.
58 . The aluminium substrate of claim 45 wherein said composition has a pH of at least about 6 to no more than about 7.
59 . The aluminium substrate of claim 45 further comprising an α-hydroxy carboxylic acid.
60 . The aluminium substrate of claim 59 wherein said α-hydroxy carboxylic acid is present at a concentration of no more than about 5%, by weight.
61 . The aluminium substrate of claim 59 wherein said α-hydroxy carboxylic acid is selected from a group consisting of malic acid, tartartic acid and citric acid.
62 . The aluminium substrate of claim 61 wherein said α-hydroxy carboxylic acid is tartartic acid.
63 . An electrolytic composition comprising 0.1% and 1%, by weight, sodium silicate and 0.1% and 1%, by weight, a compound selected from a group consisting aspartic acid and glutamic acid wherein said electrolytic solution is at a pH of about 5 to about 7.Join the waitlist — get patent alerts
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