The present invention relates to a method for coating a turbomachine part with a paint, for example an anti-corrosion paint, implementing a step of deposition by electrophoresis.
High-strength steels, such as Managing 250 or ML340, can be used to form turbomachine parts. However, in use, these steels can be sensitive to corrosion. In order to protect the parts from corrosion, it is known to coat them with anti-corrosion paints sprayed using a spray gun. With this type of method, controlling the thickness of applied paint can be relatively delicate, in particular if the part has a complex geometry. Non-compliant coatings having an unsatisfactory corrosion resistance may therefore be obtained.
It is therefore desirable to have a method for depositing a coating, for example an anti-corrosion coating, which makes it possible to obtain, in a simple manner, a coating having the desired properties, for example a satisfactory anti-corrosion protection.
The invention relates to a method for coating a turbomachine part, comprising:
For conciseness, the expressions “first voltage stabilization phase” and “second voltage stabilization phase” are respectively designated hereinafter by “first phase” and “second phase”, The ratio R [duration of the first phase]/[duration of the first phase+duration of the second phase] will in turn be designated hereinafter by the expression “ratio R”.
Through the use of the pulsed voltage cycles described above, the invention makes it possible to achieve a uniform and dense coating conferring, for example, a satisfactory protection against corrosion. The invention makes it possible, in particular, to avoid the phenomena of “bubbling” of the electrolyte associated with the electrolysis of water which may be encountered when a DC voltage is imposed during electrophoresis. This “bubbling” phenomenon leads to a much less uniform and therefore significantly less efficient coating. The invention is based on the implementation of an electrophoresis technique with specific electrical parameters, which enables the desired coating to be obtained in a simple manner. The electrophoresis technique implemented in the invention also provides better control of the thickness of the coating deposited in comparison to spraying using a spray gun. It is thus of particular interest for coating parts having a complex geometry.
In an embodiment, the absolute value of the first potential difference is less than or equal to 15 V.
The use of a first potential difference with limited absolute value makes it possible to further improve the uniformity of the obtained coating.
In particular, the absolute value of the first potential difference may be less than or equal to 10 V, for example less than or equal to 7 V. The absolute value of the first potential difference can be between 2 V and 15 V, for example between 2 V and 10 V, for example between 5 V and 10 V, for example between 5 V and 7 V or between 2 V and 7 V.
In an embodiment, the absolute value of the second potential difference is less than or equal to 5 V.
The use of a second potential difference with limited absolute value makes it possible to further improve the uniformity of the obtained coating.
In an embodiment, the ratio R is between 1:10 and 1:3.
The use of these values for the ratio R makes it possible to further improve the uniformity of the coating obtained.
In particular, the ratio R can be between 1:10 and 1:4. The ratio R can also be between 1:6 and 1:3 or between 1:6 and 1:4.
In an embodiment, the pulsed voltage cycles are repeated with a frequency less than or equal to 1 kHz during the deposition by electrophoresis.
The fact of limiting the frequency of repetition of the pulsed voltage cycles is advantageous in order to increase the relaxation time of the system between two successive first phases, which enables the uniformity of the coating obtained to be further improved.
In particular, said frequency can be less than or equal to 100 Hz, or even less than or equal to 10 Hz.
In an embodiment, the paint is inorganic.
The use of an inorganic paint is advantageous when the turbomachine part is intended to operate at relatively high temperatures, outside of the stability range for organic paints.
In an embodiment, the paint is an anti-corrosion paint.
In an embodiment, the part is an aircraft turbomachine part.
With reference to
The surface of the part 1 intended to be coated comprises an electrically conductive material. The part 1 can be made of a metal material, for example aluminum or an aluminum alloy, steel or a nickel- or cobalt-based superalloy. The part 1 may be an aircraft turbomachine part. The part 1 may be a turbomachine blade, such as a turbine blade or a compressor blade, a turbine shaft or a portion of a turbine shaft, a compressor shaft for a portion of a compressor shaft.
The part 1 constitutes an electrode which is connected to a first terminal of a voltage generator G. A counter electrode 20 is present facing the surface of the part 1 to be coated and is also immersed in the bath of paint 10. The counter electrode 20 is connected to a second terminal of the voltage generator G, different from the first terminal.
During the deposition by electrophoresis, the generator G imposes specific pulsed voltage cycles between the part 1 and the counter electrode 20 which are described in more detail in the following, with reference to
A commercial paint 10 that is known per se can be used. The paint 10 is typically in the form of a suspension comprising solid particles 11 dispersed in a liquid medium. Advantageously, the paint 10 can be devoid of chromium in oxidation state +VI in order to be compatible with the regulations on “Registration, Evaluation, Authorization and Restriction of Chemicals” (“REACH”). The paint 10 can contain chromium in oxidation state +III. An example of usable paint 10 is the paint marketed by PRAXAIR under the name SERMETEL W®.
The particles 11 of the paint 10 can comprise one or more pigments, for example one or more anti-corrosion pigments in the case of an anti-corrosion paint. These pigments are typically chosen from: metal phosphates, for example zinc phosphate; metal chromates, such as magnesium chromate; or halogen-zirconates; or the mixtures of such compounds. Electrically conductive particles, such as aluminum particles, can be added to the pigment or pigments. The addition of these conductive particles makes it possible to give the layer 6 an electrically conductive nature, which makes it possible to avoid a self-limiting effect of the deposition by electrophoresis and makes it possible, if desired, to deposit a relatively thick layer 6.
In the case where such conductive particles are not present, the treated surface can become gradually more and more insulating during the deposition of the layer 6, naturally slowing, or even stopping, its formation. By way of illustration, the thickness e of the deposited layer 6 can be greater than or equal to 35 μm, for example between 35 μm and 70 μm.
By way of illustration, the average size D50 of, possibly agglomerated, particles 11 of the paint 10 can be less than or equal to 10 μm, for example between 0.1 μm and 10 μm. The liquid medium of the paint can typically contain a binder and a solvent. The paint 10 may optionally further comprise one or more additives for adjusting its properties, such is its viscosity or the stability of the suspension.
During the deposition, the generator G imposes a variable potential difference between the part 1 and the counter electrode 20. Due to the application of an electric field between the part 1 and the counter electrode 20, the electrically charged paint particles 11 move and are deposited on the part 1 in order to obtain the layer 6. The example illustrated in
The preceding description has attempted to describe the electrophoresis system and the formation of the layer 6 with reference to
According to the example of
During the deposition by electrophoresis, there is an alternation between the first voltage stabilization phases P1 and the second voltage stabilization phases P2. Hence, there is, successively: performance of a first voltage stabilization phase P1 of a first cycle, then a second voltage stabilization phase P2 of this first cycle, then performance of a first voltage stabilization phase P1 of a second cycle, then a second voltage stabilization phase P2 of this second cycle and so on.
As indicated above, the relative durations of the first phases P1 and the second phases P2 are controlled within the scope of the invention. Hence, for each pulsed voltage cycle C1, the ratio R, which corresponds to the ratio T1/[T1+T2], is fixed at a predetermined value between 1:10 and 1:2, where T1 designates the duration of the first phase P1 and T2 the duration of the second phase P2. The ratio R is, for example, between 1:6 and 1:4.
The pulsed voltage cycles C1 can be repeated periodically during the deposition by electrophoresis, as illustrated. The frequency of repetition of the pulsed voltage cycles can be less than or equal to 1 kHz, for example less than or equal to 100 Hz, for example less than or equal to 5 Hz. This frequency can be between 0.1 Hz and 1 kHz, for example between 0.1 Hz and 100 Hz, for example between 1 Hz and 100 Hz, for example between 1 Hz and 10 Hz, or even between 1 Hz and 5 Hz. The pulsed voltage cycles C1 can be applied for a duration greater than or equal to 1 minute. This duration can be less than or equal to 30 minutes, for example less than or equal to 10 minutes. This duration can be between 1 minute and 30 minutes, for example between 1 minute and 10 minutes.
In general, the ratio R can vary between 1:10 and 1:2. It will be noted that for relatively high values of R, close to 1:2, it may be preferable to use first potential differences that are limited in absolute value, in order to improve the uniformity of the layer formed.
The method of the invention can be implemented for coating a turbomachine blade 21 having, for example, a root 22, an airfoil 24 and a head 26, as illustrated highly schematically in
An anti-corrosion paint was deposited using an electrophoresis system with two electrodes, comprising a platinum electrode and a 15CDV6 steel electrode. The deposited anti-corrosion paint was the paint marketed by PRAXAIR under the name SERMETEL W®.
A first test according to the invention was carried out by imposing a sequence of post-voltage cycles, each pulsed voltage cycle had a positive first voltage stabilization phase at 10 V and a second voltage stabilization phase at 0 V. The part icy to be coated was positively charged during the first phases. Each pulsed voltage cycle had a ratio R of 1:3. The voltage cycles were repeated at a frequency of 1 Hz and the deposition by electrophoresis was performed for a duration of 5 minutes.
By way of comparison, a second test outside of the scope of the invention was performed with the same electrophoresis system but by imposing a DC voltage at 10 V for a period of 1 minute 40 seconds (no alternation with second phases at zero voltage). This duration of 1 minute 40 seconds corresponds to the accumulated duration of application of the voltage of 10 V during the first test (=5 minutes/3).
It can be seen that the deposition associated with
Additional tests were carried out using the same electrophoresis system as in example 1 and by using the same sequence of pulsed voltage cycles as in the first test described in example 1 with the exception of the ratio R which was modified.
In these two cases, a particularly uniform anti-corrosion deposition was obtained, having an even better uniformity compared to that of the first test of example 1 using a ratio R of 1:3.
Additional tests were carried out using the same electrophoresis system as in example 1 and by using the same sequence of pulsed voltage cycles as in the first test described in example 1 with the exception of the value of the voltage of the first phases which was modified.
In these two cases, a particularly uniform anti-corrosion deposition was obtained, having an even better uniformity compared to that of the first test of example 1 using a voltage of 10 V during the first phases.
Additional tests were carried out using the same electrophoresis system as in example 1 and by using the same sequence of pulsed voltage cycles as in the first test described in example 1 with the exception of the value of the voltage of the second phases which was modified.
In this case, a particularly uniform anti-corrosion deposition was obtained, having an even better uniformity compared to that of the first test of example 1 using a voltage of 0 V during the second phases.
Additional tests were carried out using the same electrophoresis system as in example 1 and by using the same sequence of pulsed voltage cycles as in the first test described in example 1 with the exception of the duration of the deposition by electrophoresis which was fixed at 1 minute. Several voltage values of the first phases were evaluated with this treatment duration, namely: 10 V (
In all cases, it was observed that an anti-corrosion deposition having good uniformity was obtained.
Additional tests were carried out using the same electrophoresis system as in example 1 and by using the same sequence of pulsed voltage cycles as in the first test described in example 1 with the exception of the duration of the deposition by electrophoresis which was fixed at 1 minute and of the frequency which was modified.
In all cases, it was observed that an anti-corrosion deposition having good uniformity was obtained.
The expression “between . . . and . . . ” should be understood as including the limits.
Number | Date | Country | Kind |
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FR1909158 | Aug 2019 | FR | national |
Filing Document | Filing Date | Country | Kind |
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PCT/FR2020/051406 | 7/30/2020 | WO |