The present disclosure relates to bearings and, more particularly, automotive parts coated with iron oxide for electric drive unit bearings of vehicles.
Black oxide coatings are used to suppress white etching cracks by acting as a hydrogen diffusion barrier between the base metal and the lubricant. Black oxide coatings are also used as an insulating layer to lessen bearing failures associated with electrical damage. However, many process steps are involved and cycle times are relatively long.
Thus, while current systems and methods of coating an automotive part with black oxide coating achieve their intended purpose, there is a need for a new and improved system and method of coating an automotive part black (iron) oxide for an electric drive unit of a vehicle.
In one aspect of the present disclosure, a method of coating an automotive part with iron oxide for an electric drive unit of a vehicle is provided. The method comprises providing an automotive part comprising a body having an outer surface. The part comprises steel. The method further comprises introducing the part in an aqueous coating solution comprising sodium metabisulfite, an ionic surfactant, and citric acid to form residual oxides on the outer surface of the part defining a sample-water interface.
The method further comprises emitting ultrasonic waves in the coating solution to generate acoustic cavitation activity at the sample-water interface and continuously form oxygen and hydrogen species. The citric acid is arranged to chemically activate the steel surface and to allow for the reaction with the oxygen and hydrogen species to form iron hydroxide. The sodium metabisulfite is arranged to react with the iron hydroxide and generate iron oxysulfide on the outer surface such that the iron oxysulfide reacts with the oxygen and hydrogen species and produces iron oxides (FeO, Fe2O3, Fe3O4) and iron sulfide (FeS) on the outer surface. The iron oxides and iron sulfide define a black oxide coating having iron sulfide platelets disposed thereon.
In one example, the method further comprises, prior to introducing the part in the coating solution, cleaning the part to remove residual oil from the outer surface. In another example, cleaning comprises disposing the part in a cleaning solution and emitting ultrasonic waves on the outer surface. In yet another example, the method further comprises rinsing the cleaning solution from the outer surface.
In another example, the method further comprises rinsing the black oxide coating of the outer surface with an aqueous solution to remove the cleaning solution therefrom and drying the outer surface to remove the aqueous solution from the black oxide coating. In yet another example, the coating solution comprises between 5 weight (wt) percent (%) and 20 wt % sodium metabisulfite, between 3 wt % and 15 wt % ionic surfactant, and between 0.25 wt % and 3 wt % citric acid.
In one example, the coating solution is at between 15 degrees Celsius (° C.) and 40° C. In another example, emitting ultrasonic waves on the part has a duration of between 1 minute (min) and 20 mins at a frequency of between 15 kilohertz (KHz) and 400 kHz. In yet another example, the black oxide coating has a thickness of between 1 micron and 4 microns.
In accordance with another aspect of the present disclosure, a system for coating an automotive part with iron oxide for an electric drive unit of a vehicle is provided. The system comprises an automotive part comprising a body having an outer surface, the part comprising steel. The system further comprises an introducer mechanism arranged to suspend the part in an aqueous coating solution comprising sodium metabisulfite, an ionic surfactant, and citric acid to form residual oxides on the outer surface of the part defining a sample-water interface.
The system further comprises an ultrasonic mechanism arranged to emit ultrasonic waves in the coating solution to generate acoustic cavitation activity at the sample-water interface and continuously form oxygen and hydrogen species from the residual oxides. The citric acid is arranged to chemically activate the steel surface and to allow for the reaction with the oxygen and hydrogen species to form iron hydroxide. The sodium metabisulfite is arranged to react with the iron hydroxide and generate iron oxysulfide on the outer surface such that the iron oxysulfide reacts with the oxygen and hydrogen species producing iron oxides (FeO, Fe2O3, Fe3O4) and iron sulfide (FeS) on the outer surface to define a black oxide coating having iron sulfide platelets disposed thereon.
In one embodiment, the system further comprises a cleaning unit arranged to clean the part to remove residual oil from the outer surface defining the outer surface comprising the residual oxides. In another embodiment, the cleaning unit is arranged to dispose the part in a cleaning solution and emit ultrasonic waves thereon. In yet another embodiment, the cleaning unit is arranged to rinse the cleaning solution from the outer surface.
In another embodiment, the system further comprises a rinsing unit arranged to rinse the black oxide coating of the outer surface with an aqueous solution to remove the cleaning solution therefrom. The system further comprises a drying mechanism arranged to dry the outer surface to remove the aqueous solution therefrom.
In one embodiment, the coating solution comprises between 5 weight (wt) percent (%) and 20 wt % sodium metabisulfite, between 3 wt % and 15 wt % ionic surfactant, and between 0.25 wt % and 3 wt % citric acid. In another embodiment, the coating solution is at between 15 degrees Celsius (° C.) and 40° C. In yet another embodiment, emitting ultrasonic waves on the part has a duration of between 1 minute (min) and 20 mins at a frequency of between 15 kilohertz (kHz) and 400 kHz. In still another embodiment, the black oxide coating has a thickness of between 1 micron and 4 microns.
In accordance with yet another aspect of the present disclosure, an automotive part for an electric drive unit of a vehicle is provided. The automotive part comprises an automotive part comprising a body having an outer surface. The body comprises steel and the outer surface comprising a black oxide coating. The black oxide coating comprising an iron oxide film and iron sulfide platelets disposed thereon. In one embodiment, the black oxide coating has a thickness of between 1 micron and 4 microns.
Further areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.
The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.
The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses.
Embodiments and examples of the present disclosure provide a new and improved system and method of coating an automotive part with black (iron) oxide for an electric drive unit of a vehicle. The automotive part may be a ball bearing assembly for a rotating shaft of an electric drive unit. The automotive part comprises a body and an outer wherein the outer surface is coated with a black oxide coating comprising an iron oxide film and iron sulfide platelets disposed on the iron oxide film. As a result, the systems and methods of the present disclosure involve reduced process steps. Moreover, the systems and methods have a reduced cycle time of between about 5 mins and 20 mins.
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More specifically, the coating solution 30 may comprise between 5 weight (wt) percent (%) and 20 wt %, 6 wt %, 7 wt %, 8 wt %, 10 wt %, 12 wt %, 14 wt %, 16 wt %, and 18 wt % sodium metabisulfite (Na2SO3). Moreover, the coating solution 30 may comprise between 3 wt % and 15 wt %, 4 wt %, 5 wt %, 6 wt %, 7 wt %, 8 wt %, 9 wt %, 10 wt %, 11 wt %, 12 wt %, 13 wt %, and 14 wt % surfactant. The surfactant may be a liquid detergent comprising a chlorosulfonated hydrocarbon, sodium dodecyl benzene sulphonate, or any other suitable solution without departing from the spirit of scope of the present disclosure. Additionally, the coating solution 30 may comprise between 0.25 wt % and 3 wt %, 0.5 wt %, 0.8 wt %, 1 wt %, 1.3 wt %, 1.5 wt %, 1.8 wt %, 2 wt %, 2.3 wt %, 2.5 wt %, and 2.8 wt % citric acid. Furthermore, the coating solution 30 in the coating tank 26 may have a temperature of between 15 degrees Celsius (° C.) and 40° C., 20° C., 25° C., 30° C., and 35° C.
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More specifically, the ultrasonic mechanism or ultrasound probe 32 is disposed in the coating solution 30 in which the part 12 is immersed. The ultrasonic mechanism 32 emits ultrasonic or sound waves through the coating solution 30 for a predetermined duration and with a predetermined frequency. Preferably, the predetermined frequency is between 15 kilohertz (kHz) and 400 kHz and more preferably between 20 KHz and 40 kHz. In other embodiments, the predetermined frequency may be 25 kHz, 30 KHz, 35 kHz, 45 kHz, 50 kHz, 55 kHz, 60 kHz, 70 kHz, 80 kHz, 100 kHz, 200 kHz, and 300 kHz. Furthermore, the predetermined duration may be between 1 minute (min) and 20 mins, 2 mins, 3 mins, 4 mins, 5 mins, 10 mins, and 15 mins.
In turn, acoustic cavitation bubbles are generated in the coating solution 30 at the sample-water interface 31. The acoustic cavitation bubbles undergo a sequence of dynamics in formation: bubble formation; growth in volume due to pressure and temperature; an unstable phase; and a collapse (implosion) due to excessive pressure (up to greater than 2000 ATMs) and temperature (up to greater than 5000 K) buildup in the bubbles. As a result, a dissociation of water vapor to hydroxyl and reactive oxygen/hydrogen radicals or species, including O2, H2O2, OH, H, HO2, O, and H2, occur. Such oxygen/hydrogen species are combined by chemical reactions to form hydrogen and oxygen molecules, hydrogen peroxide, and other reactive species. The chemical reactions may include:
where H2O is water in the aqueous coating solution 30, *OH is hydroxide radical, H* is hydrogen radical, H2 is hydrogen, O is oxygen atom, O2 is oxygen molecule, HO2 is hydroperoxyl.
In this example, the citric acid is arranged to chemically activate the steel surface and to allow for the reaction with oxygen/hydrogen species and iron (Fe) ions at the sample-water interface 31 forming iron hydroxide, Fe(OH)2. Moreover, the sodium metabisulfite is arranged to react with the iron hydroxide generating iron oxysulfide (FeSO3) at the sample-water interface 31 on the outer surface 20. In turn, the iron oxysulfide reacts with oxygen/hydrogen species to produce an iron oxide (FeO, Fe2O3, Fe3O4) film 34 and iron sulfide (FeS) platelets 36 on the outer surface 20. That is, a first portion of the iron oxysulfide reacts with oxygen to produce the iron oxide film 34 on the outer surface 20. Additionally, a second portion of the iron oxysulfide reacts with hydrogen to produce the iron sulfide platelets 36 disposed in the iron oxide film 34.
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As a result, the system 10 of the present disclosure involves reduced process steps. Moreover, the system 10 has a reduced cycle time of between about 5 mins and 20 mins.
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More specifically, the coating solution 30 may comprise between 5 weight (wt) percent (%) and 20 wt %, 6 wt %, 7 wt %, 8 wt %, 10 wt %, 12 wt %, 14 wt %, 16 wt %, and 18 wt % sodium metabisulfite (Na2SO3). Moreover, the coating solution 30 may comprise between 3 wt % and 15 wt %, 4 wt %, 5 wt %, 6 wt %, 7 wt %, 8 wt %, 9 wt %, 10 wt %, 11 wt %, 12 wt %, 13 wt %, and 14 wt % surfactant. The surfactant may be a liquid detergent comprising a chlorosulfonated hydrocarbon, sodium dodecyl benzene sulphonate, or any other suitable solution without departing from the spirit or scope of the present disclosure. Additionally, the coating solution 30 may comprise between 0.25 wt % and 3 wt %, 0.5 wt %, 0.8 wt %, 1 wt %, 1.3 wt %, 1.5 wt %, 1.8 wt %, 2 wt %, 2.3 wt %, 2.5 wt %, and 2.8 wt % citric acid. Furthermore, the coating solution 30 in the coating tank 26 may have a temperature of between 15 degrees Celsius (C) and 40° C., 20° C., 25° C., 30° C., and 35° C.
The method 110 further comprises in box 120 emitting ultrasonic waves in the coating solution 30. As in the system 10 of
More specifically, the ultrasonic mechanism 32 or ultrasound probe is disposed in the coating solution 30 in which the part 12 is immersed. The ultrasonic mechanism 32 emits ultrasonic or sound waves through the coating solution 30 for a predetermined duration and with a predetermined frequency. Preferably, the predetermined frequency is between 15 kilohertz (kHz) and 400 kHz and more preferably between 20 kHz and 40 kHz. In other embodiments, the predetermined frequency may be 25 kHz, 30 KHz, 35 kHz, 45 kHz, 50 KHz, 55 kHz, 60 kHz, 70 kHz, 80 kHz, 100 kHz, 200 kHz, and 300 kHz. Furthermore, the predetermined duration may be between 1 minute (min) and 20 mins, 2 mins, 3 mins, 4 mins, 5 mins, 10 mins, and 15 mins.
In turn, acoustic cavitation bubbles are generated in the coating solution 30 at the sample-water interface 31. The acoustic cavitation bubbles undergo a sequence of dynamics in formation: bubble formation; growth in volume due to pressure and temperature; an unstable phase; and a collapse (implosion) due to excessive pressure (up to greater than 2000 ATMs) and temperature (up to greater than 5000 K) buildup in the bubbles. As a result, a dissociation of water vapor to hydroxyl and reactive oxygen/hydrogen radicals or species, including O2, H2O2, OH, H, HO2, O, and H2, occur. Such oxygen/hydrogen species are combined by chemical reactions to form hydrogen and oxygen molecules, hydrogen peroxide, and other reactive species. As in the system 10 above, the chemical reactions may include:
where H2O is water in the aqueous coating solution 30, *OH is hydroxide radical, H* is hydrogen radical, H2 is hydrogen, O is oxygen atom, O2 is oxygen molecule, HO2 is hydroperoxyl.
In this example, the citric acid is arranged to react with oxygen/hydrogen species and iron (Fe) ions at the sample-water interface 31 forming iron hydroxide, Fe(OH)2. Moreover, the sodium metabisulfite is arranged to react with the iron hydroxide generating iron oxysulfide (FeSO3) at the sample-water interface 31 on the outer surface 20. In turn, the iron oxysulfide reacts with oxygen/hydrogen species to produce an iron oxide (Fe2O3) film 34 and iron sulfide (FeS) platelets 36 on the outer surface 20. That is, a first portion of the iron oxysulfide reacts with oxygen to produce the iron oxide film 34 on the outer surface 20. Additionally, a second portion of the iron oxysulfide reacts with hydrogen to produce the iron sulfide platelets 36 disposed in the iron oxide film 34.
In this example, the iron oxide and the iron sulfide are formed on the outer surface 20 to define a black oxide coating 40 disposed on the outer surface 20. The black oxide coating 40 comprises an iron oxide film 34 and iron sulfide platelets 36 disposed thereon. In this embodiment, the black oxide coating 40 may comprise between 50 wt % and 100 wt %, 55 wt %, 60 wt %, 65 wt %, 70 wt %, 75 wt %, 80 wt %, 85 wt %, 90 wt %, and 95 wt % iron oxide. Additionally, the black oxide coating 40 may comprise between 0 wt % and 50 wt %, 10 wt %, 15 wt %, 20 wt %, 25 wt %, 30 wt %, 35 wt %, 40 wt %, and 45 wt % iron sulfide. Furthermore, the black oxide coating 40 has a thickness of between 0.5 micron and 4 microns, 1 micron, 1.5 micron, 2 microns, 2.5 microns, 3 microns, and 3.5 microns.
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As a result, the method 110 of the present disclosure involves reduced process steps. Moreover, the method 110 has a reduced cycle time of between about 5 mins and 20 mins.
The description of the present disclosure is merely exemplary in nature and variations that do not depart from the gist of the present disclosure are intended to be within the scope of the present disclosure. Such variations are not to be regarded as a departure from the spirit and scope of the present disclosure.