BACKGROUND OF THE INVENTION
[0001] The present invention relates to a corrosion resistant, chromate-free, phosphate-fluoride
conversion coating, with or without vanadate, for a product formed from magnesium
or a magnesium alloy and to a coating solution for use in a coating process.
[0002] Magnesium alloys are light and strong, but very vulnerable to corrosion due to the
reactive nature of magnesium. Magnesium alloys are protected from corrosion in all
practical applications. A commonly used, low cost, corrosion resistant treatment for
magnesium alloys is a dichromate based conversion coating. While dichromate based
conversion coatings provide good corrosion protection, they are based on a chemical
compound (hexavalent chromium) that has many occupational exposure risks. A non-chromate,
corrosion resistant magnesium conversion coating is required to meet industry demands.
[0003] Another treatment for protecting magnesium or magnesium alloy products is shown in
U.S. Patent No. 5,683,522 to Joesten. In this treatment, a paint adherent and corrosion
resistant coating of magnesium phosphate and magnesium fluoride is applied to a product
formed from a magnesium alloy. The process for applying the coating involves immersing
the magnesium alloy product in a solution having phosphate and fluoride ions. This
treatment while providing a barrier film and very good paint adhesion, does not include
electrochemically active ingredients to suppress corrosion. U.S. Patent Application
Publication No. 2003/0150525 discloses an improved phosphate-fluoride corrosion coating
for magnesium and process for applying same.
[0004] It is an object of the present invention to provide an improved chromate-free corrosion
resistant conversion coating for magnesium and magnesium alloy products.
[0005] It is a further object of the present invention to provide a coating solution for
forming the chromate-free corrosion resistant coating.
SUMMARY OF THE INVENTION
[0006] The foregoing objects are attained by the present invention.
[0007] In accordance with the present invention, a chromate-free, phosphate-fluoride conversion
coating, with or without vanadate, formed on a magnesium or a magnesium alloy substrate,
includes an active corrosion inhibitor selected from the group consisting of organo-phosphonic
acids. The phosphonic acid group reacts with the magnesium metal of the substrate
to form an insoluble salt. The preferred organo-phosphonic acids used as corrosion
inhibitors in accordance with the present invention are selected from the group consisting
of straight chain or branched amino alkyl phosphonic acids, straight chain or branched
alkyl phoshonic acids, and triphosphonic acids, particularly, nitrilotris (methylene)
triphosphonic acid (NTMP). When the corrosion inhibitor includes amino alkyl phosphonic
acids, the amine group can interact with vanadate ions in the coating solution to
increase the vanadate incorporation into the conversion coating.
[0008] Other details of the magnesium-magnesium alloy conversion coating of the present
invention, as well as objects and advantages attended thereto, are set forth in the
following detailed description.
DETAILED DESCRIPTION
[0009] In accordance with the present invention, a solution for forming a chromate-free,
corrosion resistant coating on a magnesium or magnesium alloy substrate comprises
a solution having phosphate and fluoride ions and, an active corrosion inhibitor selected
from the group consisting of organo-phosphonic acids.
[0010] The solution of the present invention may optionally include vanadate anions. The
active corrosion inhibitor is selected from the group consisting of straight chained
or branched amino-alkyl phosphonic acids, straight chained or branched alkyl phosphonic
acids, triphosphonic acids, and mixtures thereof. A particular useful triphosphonic
acid comprises nitrilotris (methylene) triphosphonic acid (NTMP).
[0011] As noted above, the chromate-free solution include phosphate and fluoride ions. Phosphate
and fluoride ions are present in an amount of between about 1 g/L to 50 g/L and 1
g/L to 10 g/L, respectively, preferably between 10 g/L to 25 g/L and 3 g/L to 5 g/L,
respectively. It is important in the present invention to control the pH of the solution
and this is achieved by the amount of phosphate ions and fluoride ions in the solution.
The pH of the solution is preferably in the range of 5 to 7. The particular phosphate
and fluoride compounds employed in forming the solution having the appropriate pH
is disclosed in detail in U.S. Patent Application Publication No. 2003/0150525 to
which suitable reference can be made. As mentioned therein, suitable phosphate compounds
include monobasic potassium phosphate (KH
2PO
4), dibasic potassium phosphate (K
2HPO
4), tribasic potassium phosphate (K
3PO
4), or phosphoric acid (H
3PO
4), or combinations of these alternatives. A preferred embodiment is a combination
of monobasic potassium phosphate and dibasic potassium phosphate. Suitable fluoride
compounds include sodium bifluoride (NaHF
2). In a preferred embodiment, the concentration is provided at about 0.3-0.5% by weight
sodium bifluoride. Other fluoride compounds, such as potassium fluoride or hydrofluoric
acid, may also be used.
[0012] In accordance with the present invention, the corrosion inhibitor is present in the
solution in an amount of between about 1 ppm to 1 wt%, preferably 10 ppm to 0.5 wt%.
The corrosion inhibitor is in the form of an organo-phosphonic acid. Preferred organo-phosphonic
acids include straight chained and branched amino-alkyl phosphonic acids, straight
chained or branched alkyl phosphonic acids and triphosphonic acids. A particularly
useful triphosphonic acid is nitrilotris (methylene) triphosphonic acid (NTMP).
[0013] In accordance with the present invention, the solution may optionally include vanadate
anions. Sodium vanadate is a suitable source of vanadate ions for the solution of
the present invention. In accordance with the present invention, the vanadate ions
are present in an amount of between about 1.0 g/l to 5.0 g/l. It has been found that
the vanadate anions interact with the amine group of the amino alkyl phosphonic acids
increase incorporation of the vanadate into the conversion coating thereby improving
the coating performance. In addition, the phosphonic acid groups of the corrosion
inhibitor react with the magnesium metal substrate to form insoluble salts which improve
corrosion performance.
[0014] The preferred chromate-free solution comprises phosphate ions in an amount of between
10 to 25 g/L, fluoride ions in an amount of between 3 g/L to 5 g/L, vanadate anions
in an amount of between 1 g/L to 5 g/L, and the corrosion inhibitor in an amount of
between 10 ppm to 0.5 wt%.
[0015] A magnesium or magnesium alloy substrate having a conversion coating in accordance
with the present invention comprises mostly magnesium phosphate and magnesium fluoride.
It is believed that the amino alkyl phosphonic acid will form insoluble magnesium
salt as part of the conversion coating. This component will increase the interaction
of vanadium with conversion coating, therefore increase vanadium content in the coating,
should vanadium is used as corrosion inhibitor as well.
[0016] It is to be understood that the invention is not limited to the illustrations described
and shown herein, which are deemed to be merely illustrative of the best modes of
carrying out the invention, and which are susceptible of modification of form, size,
arrangement of parts and details of operation. The invention rather is intended to
encompass all such modifications which are within its scope as defined by the claims.
1. A solution for forming a chromate-free, corrosion resistant coating on a product formed
from magnesium or a magnesium alloy, comprising:
the solution having phosphate and fluoride ions; and
an active corrosion inhibitor selected from the group consisting of organo-phosphonic
acids.
2. A solution according to claim 1, wherein the organo-phosphonic acid is selected from
the group consisting of straight chained amino-alkyl phosphonic acids, branched amino-alkyl
phosphonic acids, straight chained alkyl phosphonic acids, branched alkyl phosphonic
acids, triphosphonic acids, and mixtures thereof.
3. A solution according to claim 2, wherein the triphosphonic acids comprise nitrilotris
(methylene) triphosphonic acid (NTMP).
4. A solution according to any one of the preceding claims, wherein the solution includes
vanadate.
5. A solution according to any one of the preceding claims, wherein the solution comprises
1 ppm to 1 wt% of the corrosion inhibitor, preferably 10 ppm to 0.5 wt%.
6. A solution according to claim 5, wherein phosphate ions are present in an amount of
between 1 g/L to 50 g/L, preferably between 10 g/L to 25 g/L, and the fluoride ions
are present in an amount of 1 g/L to 10 g/L, preferably 3 g/L to 5 g/L.
7. A process for preparing a corrosion-resistant, chromate free, coating on a magnesium
or magnesium alloy substrate comprising treating the substrate with a solution as
defined in any one of the preceding claims, wherein the phosphonic acid group reacts
with magnesium metal forming an insoluble salt.
8. An article comprising a magnesium or magnesium alloy substrate and a corrosion resistant
coating obtainable by the process as defined in claim 7.