WO2018132233A1 - Sealing anodized aluminum using a low-temperature nickel-free process - Google Patents

Sealing anodized aluminum using a low-temperature nickel-free process Download PDF

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Publication number
WO2018132233A1
WO2018132233A1 PCT/US2017/067493 US2017067493W WO2018132233A1 WO 2018132233 A1 WO2018132233 A1 WO 2018132233A1 US 2017067493 W US2017067493 W US 2017067493W WO 2018132233 A1 WO2018132233 A1 WO 2018132233A1
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composition
sealing
ppm
complexing agent
anodized
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PCT/US2017/067493
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French (fr)
Inventor
Sara SALSA
Patrizia ANGELI
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MacDermid Acumen Inc
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MacDermid Acumen Inc
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Priority to JP2019536069A priority Critical patent/JP6811868B2/en
Priority to CN201780083121.9A priority patent/CN110168138A/en
Priority to KR1020197023349A priority patent/KR102255583B1/en
Priority to EP17891421.4A priority patent/EP3545117A4/en
Publication of WO2018132233A1 publication Critical patent/WO2018132233A1/en
Anticipated expiration legal-status Critical
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02—Anodisation
    • C25D11/04—Anodisation of aluminium or alloys based thereon
    • C25D11/18—After-treatment, e.g. pore-sealing
    • C25D11/24—Chemical after-treatment
    • C25D11/246—Chemical after-treatment for sealing layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00—Processes for applying liquids or other fluent materials
    • B05D1/36—Successively applying liquids or other fluent materials, e.g. without intermediate treatment
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/40—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing molybdates, tungstates or vanadates
    • C23C22/42—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing molybdates, tungstates or vanadates containing also phosphates
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/40—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing molybdates, tungstates or vanadates
    • C23C22/44—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing molybdates, tungstates or vanadates containing also fluorides or complex fluorides
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/82—After-treatment
    • C23C22/83—Chemical after-treatment
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02—Anodisation
    • C25D11/04—Anodisation of aluminium or alloys based thereon

Definitions

  • the invention generally relates to a method for sealing anodized aluminum surfaces to protect the surfaces from corrosion.
  • Anodizing is a process which has long been used to protect the surface of aluminum components from corrosion.
  • the process consists of making a component anodic in an acidic solution.
  • a typical anodizing process consists of degreasing, pickling/etching (or brightening), desmutting, anodizing, sealing and aging steps.
  • the process of anodization leads to the formation of a porous oxide layer on the aluminum surface which may have a thickness in the range of 3 to 25 microns depending on the field of application. Because the oxide layer is porous, it is necessary to seal the pores to prevent corrosion.
  • One method uses hot water (typically used at boiling point) for sealing porous oxide layers.
  • hot water typically used at boiling point
  • the required immersion time to achieve complete sealing of the surface is between 2 and 3 minutes per micron of oxide coating, which can lead to overall lengthy immersion times.
  • using hot water for sealing is not energy efficient and there are obvious safety hazards involved with the use of boiling water.
  • the oxide layer is often not homogeneous on aluminum alloys with high amounts of silicon. Due to the non-uniformity of the oxide layer, such alloys cannot be successfully treated using hot water because the resulting corrosion performance will not be adequate.
  • low temperature sealing processes have been developed using nickel salts, typically using nickel fluoride. These processes operate at low temperatures, typically less than 30°C, and involve a contact time of about 1 minute per micron of oxide on the aluminum surface.
  • the sealing process is thought to be accomplished via the formation of a complex of nickel aluminum - fluoride salt in the pores of the anodized coating.
  • Nickel based sealing processes have obvious advantages in terms of production throughput and energy efficiency. Furthermore, using nickel based sealing processes provides good corrosion resistance, especially for those aluminum alloys higher in silicon. However, the use of nickel is becoming increasingly restricted due to its carcinogenic properties; therefore a low temperature sealing process that does not contain nickel is desirable for providing corrosion resistance on anodized aluminum surfaces. Additionally, because of the toxicity of nickel, measures must be taken to carefully treat the wastewater from nickel based sealing processes, which can be very expensive.
  • the current invention provides a two-step process wherein the composition of the first step comprises lithium ions and fluoride ions and the composition of the second step comprises tungsten, molybdenum, titanium, zirconium, or vanadium ions.
  • This process allows for successful sealing of anodized aluminum alloys, including alloys with high silicon content.
  • the sealing of the anodized aluminum alloys is achieved at a low temperature, reduced immersion time and in the absence of nickel in the sealing composition.
  • Surfaces treated with the inventive process have excellent corrosion resistance and performance equivalent to traditional nickel based cold-sealing processes in standardized testing.
  • the current invention is summarized as a method for sealing an anodized aluminum or anodized aluminum alloy surface comprising:
  • a method for the low temperature sealing of the surface of anodized aluminum and anodized aluminum alloys, including those with high-silicon content.
  • the method involves two steps that result in excellent corrosion resistance of anodized aluminum components that do not comprise nickel and can be carried out at low temperatures.
  • the first step seals the anodized surface and the second step passivates the surface to impart excellent corrosion resistance to the surface.
  • the inventive process is more environmentally friendly and energy efficient in comparison to cold-sealing nickel and hot water sealing processes.
  • the process according to the invention can be used for sealing the surface of a wide variety of anodized aluminum and anodized aluminum alloys, including those with silicon content of 1 % or higher.
  • the process can be used for both colored and uncolored anodized surfaces of aluminum and aluminum alloys.
  • the anodized surfaces of aluminum and aluminum alloys are colored by traditional processes such as integral coloring, absorptive coloring, reactive coloring, electrochemical coloring, or interference coloring.
  • the current invention additionally reduces the bleeding of such colors that occurs with high temperature processes.
  • the anodized aluminum component to be sealed is immersed in a sealing composition containing a soluble lithium salt sufficient to provide a lithium ion concentration of between 100 and 2000 ppm, preferably between 300 and 800 ppm.
  • the lithium ions are preferably provided from lithium-acetate or lithium-fluoride, but any soluble salt of lithium can be used.
  • the sealing composition must also contain fluoride ions in a concentration of between 100 and 2000 ppm of fluoride, preferably between 150 and 800 ppm.
  • anhydrous wherein the lithium acetate is present in the sealing composition in a concentration of between 3000 to 8000 ppm and the fluoride ions are supplied from potassium- fluoride (anhydrous), wherein the potassium- fluoride is present in the composition in a concentration of between 450 to 2400 ppm.
  • the sealing composition will also preferably contain a complexing agent.
  • Suitable complexing agents include phosphines, phosphonates and polymers of acrylic acids.
  • the complexing agent may be present in the sealing composition in a concentration of between 10 to 10000 ppm, preferably between 50 to 500 ppm.
  • the complexing agent in the sealing solution is preferably selected from the group comprising phosphino-carboxylic acid polymers, phosphono- carboxylic acid polymers and mixtures thereof.
  • a particularly preferred complexing agent is 2- phosphonobutane-l,2,4-tricarboxylic acid (Structure 1).
  • Other suitable complexing agents include polymers of acrylic acid which may be used at similar concentrations to the phosphines and pliosphonates. Acrylic acid polymers with a molecular weight between 1,000 and 10,000 particularly useful in the current invention. A homopolymer of acrylic acid with a molecular weight around 4500 is most preferred.
  • the operating temperature of the sealing composition is between 20°C and 60°C, preferably between 35 °C and 40°C.
  • the pH of the sealing composition is between 5 and 8, preferably between 6 and 7.
  • the immersion time in the sealing composition is between 0.75 and 1.25 minutes per micron of anodized coating, and most preferably about 1 minute per micron.
  • the passivation composition comprises metal salts which provide metal ions selected from the group comprising tungsten, titanium, zirconium, and mixtures thereof.
  • Preferred examples of the metal salts are ammonium metatungstate, ammonium molybdate, ammonium tungstate, ammonium vanadate, zirconium acetate, titanium oxalate and mixtures thereof.
  • the most preferred metal salt is ammonium tungstate.
  • the metal salts are present in the passivation composition in a concentration of between 200 and 8000 ppm or more preferably between 1000 and 4000 ppm.
  • the metal ions are preferably present in the passivation composition at a concentration between 100 and 3000 ppm.
  • the passivation composition preferably contains a complexing agent.
  • Suitable complexing agents include phosphines and pliosphonates.
  • the phosphine and phosphonate complexing agent(s) may be present in the passivation composition in a concentration of between 10 and 10000 ppm, preferably at a concentration of between 50 and 500 ppm.
  • the complexing agent in the passivation composition is preferably selected from the group comprising phosphino-carboxylic acid polymers, phosphono-carboxylic acid polymers and mixtures thereof.
  • a particularly preferred phosphonate complexing agent is nitrilotrimethylene phosphonic acid (Structure 2).
  • Suitable complexing agents include polymers of acrylic acid which may be used at similar concentrations to the phosphine and phosphonate complexing agents.
  • Acrylic acid polymers with a molecular weight between 1 ,000 and 10,000 are particularly useful in the current invention.
  • a homopolymer of acrylic acid with a molecular weight around 4500 is most preferred.
  • the operating temperature of the passivation composition is between 40 °C and 80°C, preferably at a temperature of between 55 °C and 65°C.
  • the pH of the passivation composition should be between 4 and 8, preferably between 5.5 and 7.0.
  • the immersion time in the passivation composition is between 5 and 35 minutes, preferably from 10 to 25 minutes.
  • the components are rinsed and dried.
  • Nickel ion concentration 1.2 - 2 g/1
  • One black anodized panel and one natural panel were dipped in a sealing composition, as described in the sealing step of the current invention, comprising:
  • Lithium acetate 5000 ppm
  • the sealing composition has a pH between 6.0 and 7.0 and the panels were immersed for 20 minutes at 35°C.
  • the passivation composition has a pH between 5.5 and 7.0 and the panels were immersed for 20 minutes at 60°C.
  • the natural panels were additionally tested using an acetic acid salt spray test according to UNI EN ISO 9227. Again, the results obtained from the inventive process were similar to that obtained from the conventional nickel sealing process. The panels were also tested by dipping them in 50% nitric acid for 24 hours at 20°C. Again, the results using the inventive process were similar to that of the conventional nickel sealing process.
  • Aluminum alloy components comprising 5% silicon were anodized with a thickness of 20 microns of oxide. The components were then treated and tested as described in example 1. In all cases, similar results were obtained with the inventive process compared to the conventional nickel sealing process.
  • Aluminum alloy components comprising 7% silicon were anodized with a thickness of 20 microns of oxide. The components were then treated and tested as described above, in example 1. Similar results were obtained with the process of the invention and the conventional nickel containing sealing process.
  • the invention is generally disclosed herein using affirmative language to describe the numerous embodiments.
  • the invention also specifically includes embodiments in which particular subject matter is excluded, in full or in part, such as substances or materials, method steps and conditions, protocols, procedures, assays or analysis.
  • the invention is generally not expressed herein in terms of what the invention does not include, aspects that are not expressly included in the invention are nevertheless disclosed herein.
  • a number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Electrochemistry (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Sealing Material Composition (AREA)

Abstract

The inventive two-step process operates at low temperature, without any toxic heavy metals, to provide excellent sealing on anodized aluminum substrates, especially those aluminum substrates comprising silicon. The first step of the process seals the anodized surface and the second step passivates the anodized surface. The process allows for corrosion resistance in anodized aluminum and anodized aluminum alloys to be achieved that is comparable to traditional nickel based sealants, without the toxicity of nickel. The process additionally does not require any excessive temperatures, as required by hot water sealing processes. The composition used for the sealing step comprises soluble lithium ions, fluoride ions, and preferably, a complexing agent comprising phosphines, phosphonates and/or polymers of acrylic acid. The composition used for the passivation step comprises metal ions and preferably a complexing agent comprising phosphines, phosphonates and/or polymers of acrylic acid.

Description

SEALING ANODIZED ALUMINUM USING A LOW-TEMPERATURE NICKEL-FREE
PROCESS
FIELD OF THE INVENTION
The invention generally relates to a method for sealing anodized aluminum surfaces to protect the surfaces from corrosion.
BACKGROUND OF THE INVENTION
Anodizing is a process which has long been used to protect the surface of aluminum components from corrosion. The process consists of making a component anodic in an acidic solution. A typical anodizing process consists of degreasing, pickling/etching (or brightening), desmutting, anodizing, sealing and aging steps.
The process of anodization leads to the formation of a porous oxide layer on the aluminum surface which may have a thickness in the range of 3 to 25 microns depending on the field of application. Because the oxide layer is porous, it is necessary to seal the pores to prevent corrosion. One method uses hot water (typically used at boiling point) for sealing porous oxide layers. However, the required immersion time to achieve complete sealing of the surface is between 2 and 3 minutes per micron of oxide coating, which can lead to overall lengthy immersion times. Additionally, using hot water for sealing is not energy efficient and there are obvious safety hazards involved with the use of boiling water. The oxide layer is often not homogeneous on aluminum alloys with high amounts of silicon. Due to the non-uniformity of the oxide layer, such alloys cannot be successfully treated using hot water because the resulting corrosion performance will not be adequate.
In order to address the problems associated with hot water sealing processes, low temperature sealing processes have been developed using nickel salts, typically using nickel fluoride. These processes operate at low temperatures, typically less than 30°C, and involve a contact time of about 1 minute per micron of oxide on the aluminum surface. The sealing process is thought to be accomplished via the formation of a complex of nickel aluminum - fluoride salt in the pores of the anodized coating.
Nickel based sealing processes have obvious advantages in terms of production throughput and energy efficiency. Furthermore, using nickel based sealing processes provides good corrosion resistance, especially for those aluminum alloys higher in silicon. However, the use of nickel is becoming increasingly restricted due to its carcinogenic properties; therefore a low temperature sealing process that does not contain nickel is desirable for providing corrosion resistance on anodized aluminum surfaces. Additionally, because of the toxicity of nickel, measures must be taken to carefully treat the wastewater from nickel based sealing processes, which can be very expensive.
There have already been attempts to produce nickel-free, low temperature sealing systems, but none of these at present effectively addresses the problems associated with treatment of high silicon alloys. For example, Canadian Patent 2,226,418 to Koemer et al.
proposes the use of a lithium fluoride based immersion process (optionally containing molybdate, vanadate or tungstate ions) prior to a conventional hot sealing process (80-100°C). The process is claimed to reduce the immersion time required in the hot process and provide effective sealing of anodized metals. However, temperatures in excess of 80°C are still required. U.S. Patent 4,786,336 to Schoener et al. describes a low temperature (40°C) process using a composition based on fluoro-zirconates or fluoro-tungstates in combination with silicate.
However, this process does not produce satisfactory results on anodized aluminum alloys with high silicon content. There are many industrial applications in which aluminum alloys have higher than 1 % silicon where corrosion resistance is critical. Brake calipers are an excellent example of an aluminum alloy component that may comprise a high percentage of silicon, where a sufficiently sealed surface will be paramount to the corrosion resistance of the final product. Accordingly, there is a need for a nickel-free, low temperature sealing process suitable for all anodized aluminum alloys including high silicon alloys. SUMMARY OF THE INVENTION
The current invention provides a two-step process wherein the composition of the first step comprises lithium ions and fluoride ions and the composition of the second step comprises tungsten, molybdenum, titanium, zirconium, or vanadium ions. This process allows for successful sealing of anodized aluminum alloys, including alloys with high silicon content. The sealing of the anodized aluminum alloys is achieved at a low temperature, reduced immersion time and in the absence of nickel in the sealing composition. Surfaces treated with the inventive process have excellent corrosion resistance and performance equivalent to traditional nickel based cold-sealing processes in standardized testing.
The current invention is summarized as a method for sealing an anodized aluminum or anodized aluminum alloy surface comprising:
(i) contacting the anodized surface with a sealing composition comprising a source of lithium ions, a source of fluoride ions, and a complexing agent, followed by;
(ii) contacting the anodized surface with a passivation composition wherein the passivation composition comprises a source of metal ions and a complexing agent;
wherein the surface of the anodized aluminum or anodized aluminum alloy becomes corrosion resistant.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
According to this invention, a method is provided for the low temperature sealing of the surface of anodized aluminum and anodized aluminum alloys, including those with high-silicon content. The method involves two steps that result in excellent corrosion resistance of anodized aluminum components that do not comprise nickel and can be carried out at low temperatures. The first step seals the anodized surface and the second step passivates the surface to impart excellent corrosion resistance to the surface. The inventive process is more environmentally friendly and energy efficient in comparison to cold-sealing nickel and hot water sealing processes. The process according to the invention can be used for sealing the surface of a wide variety of anodized aluminum and anodized aluminum alloys, including those with silicon content of 1 % or higher. The process can be used for both colored and uncolored anodized surfaces of aluminum and aluminum alloys. The anodized surfaces of aluminum and aluminum alloys are colored by traditional processes such as integral coloring, absorptive coloring, reactive coloring, electrochemical coloring, or interference coloring. The current invention additionally reduces the bleeding of such colors that occurs with high temperature processes.
The anodized aluminum component to be sealed is immersed in a sealing composition containing a soluble lithium salt sufficient to provide a lithium ion concentration of between 100 and 2000 ppm, preferably between 300 and 800 ppm. The lithium ions are preferably provided from lithium-acetate or lithium-fluoride, but any soluble salt of lithium can be used. The sealing composition must also contain fluoride ions in a concentration of between 100 and 2000 ppm of fluoride, preferably between 150 and 800 ppm.
In a preferred embodiment the lithium ions are supplied from lithium acetate
(anhydrous), wherein the lithium acetate is present in the sealing composition in a concentration of between 3000 to 8000 ppm and the fluoride ions are supplied from potassium- fluoride (anhydrous), wherein the potassium- fluoride is present in the composition in a concentration of between 450 to 2400 ppm.
The sealing composition will also preferably contain a complexing agent. Suitable complexing agents include phosphines, phosphonates and polymers of acrylic acids. The complexing agent may be present in the sealing composition in a concentration of between 10 to 10000 ppm, preferably between 50 to 500 ppm. The complexing agent in the sealing solution is preferably selected from the group comprising phosphino-carboxylic acid polymers, phosphono- carboxylic acid polymers and mixtures thereof. A particularly preferred complexing agent is 2- phosphonobutane-l,2,4-tricarboxylic acid (Structure 1). Other suitable complexing agents include polymers of acrylic acid which may be used at similar concentrations to the phosphines and pliosphonates. Acrylic acid polymers with a molecular weight between 1,000 and 10,000 particularly useful in the current invention. A homopolymer of acrylic acid with a molecular weight around 4500 is most preferred.
Structure 1.
Figure imgf000006_0001
The operating temperature of the sealing composition is between 20°C and 60°C, preferably between 35 °C and 40°C. The pH of the sealing composition is between 5 and 8, preferably between 6 and 7. The immersion time in the sealing composition is between 0.75 and 1.25 minutes per micron of anodized coating, and most preferably about 1 minute per micron. After the sealing step, the components are rinsed and transferred to a passivating step.
Following the sealing treatment step as outlined above, the aluminum components are transferred to a second composition for passivation. The passivation composition comprises metal salts which provide metal ions selected from the group comprising tungsten, titanium, zirconium, and mixtures thereof. Preferred examples of the metal salts are ammonium metatungstate, ammonium molybdate, ammonium tungstate, ammonium vanadate, zirconium acetate, titanium oxalate and mixtures thereof. The most preferred metal salt is ammonium tungstate. The metal salts are present in the passivation composition in a concentration of between 200 and 8000 ppm or more preferably between 1000 and 4000 ppm. The metal ions are preferably present in the passivation composition at a concentration between 100 and 3000 ppm.
The passivation composition preferably contains a complexing agent. Suitable complexing agents include phosphines and pliosphonates. The phosphine and phosphonate complexing agent(s) may be present in the passivation composition in a concentration of between 10 and 10000 ppm, preferably at a concentration of between 50 and 500 ppm. The complexing agent in the passivation composition is preferably selected from the group comprising phosphino-carboxylic acid polymers, phosphono-carboxylic acid polymers and mixtures thereof. A particularly preferred phosphonate complexing agent is nitrilotrimethylene phosphonic acid (Structure 2). Other suitable complexing agents include polymers of acrylic acid which may be used at similar concentrations to the phosphine and phosphonate complexing agents. Acrylic acid polymers with a molecular weight between 1 ,000 and 10,000 are particularly useful in the current invention. A homopolymer of acrylic acid with a molecular weight around 4500 is most preferred.
Structure 2.
Figure imgf000007_0001
The operating temperature of the passivation composition is between 40 °C and 80°C, preferably at a temperature of between 55 °C and 65°C. The pH of the passivation composition should be between 4 and 8, preferably between 5.5 and 7.0. The immersion time in the passivation composition is between 5 and 35 minutes, preferably from 10 to 25 minutes.
Following the passivation step, the components are rinsed and dried.
The invention is illustrated by the following non-limiting examples:
Example 1.
Four Q- panels of aluminum alloy 6060 (maximum 0.3-0.6% silicon) were anodized with a thickness of 20 microns of oxide. Two of the Q-panels were dipped into black organic color for 10 minutes (8 g/1 of Sanodal Black 2MLW) at 50°C and the other two panels were left in a natural condition.
One black anodized panel and one natural panel were dipped in a conventional nickel fluoride based sealant for 10 minutes at 28 °C.
Nickel ion concentration: 1.2 - 2 g/1
Fluoride ion concentration: 500 ppm
One black anodized panel and one natural panel were dipped in a sealing composition, as described in the sealing step of the current invention, comprising:
Lithium acetate: 5000 ppm
Fluoride ions: 400 - 800 ppm
Complexing agent (Structure 1): 250 ppm
The sealing composition has a pH between 6.0 and 7.0 and the panels were immersed for 20 minutes at 35°C.
Then panels were then immersed in a passivation solution of the current invention, comprising;
Ammonium metatungstate: 2000 ppm
Complexing agent (Structure 2): 250 ppm
The passivation composition has a pH between 5.5 and 7.0 and the panels were immersed for 20 minutes at 60°C.
Following the passivation step, the visual aesthetics of the black panels were compared. It was found that the panel treated with the two-step process of the invention gave visually identical results to that obtained from the conventional nickel containing sealing process. The natural panels were analyzed using a weight loss test after dipping in
chromic/sulfuric acid as described in test UNI EN 12373-7. The weight loss from the panel processed using the inventive process was similar to that obtained from the conventional nickel sealing process.
The natural panels were additionally tested using an acetic acid salt spray test according to UNI EN ISO 9227. Again, the results obtained from the inventive process were similar to that obtained from the conventional nickel sealing process. The panels were also tested by dipping them in 50% nitric acid for 24 hours at 20°C. Again, the results using the inventive process were similar to that of the conventional nickel sealing process.
Example 2.
Aluminum alloy components comprising 5% silicon were anodized with a thickness of 20 microns of oxide. The components were then treated and tested as described in example 1. In all cases, similar results were obtained with the inventive process compared to the conventional nickel sealing process.
Example 3.
Aluminum alloy components comprising 7% silicon were anodized with a thickness of 20 microns of oxide. The components were then treated and tested as described above, in example 1. Similar results were obtained with the process of the invention and the conventional nickel containing sealing process.
The invention is generally disclosed herein using affirmative language to describe the numerous embodiments. The invention also specifically includes embodiments in which particular subject matter is excluded, in full or in part, such as substances or materials, method steps and conditions, protocols, procedures, assays or analysis. Thus, even though the invention is generally not expressed herein in terms of what the invention does not include, aspects that are not expressly included in the invention are nevertheless disclosed herein. A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention.

Claims

IN THE CLAIMS
A method for sealing an anodized aluminum or anodized aluminum alloy surface comprising:
(i) contacting the anodized surface with a sealing composition comprising a source of lithium ions, a source of fluoride ions, and a complexing agent, followed by;
(ii) contacting the anodized surface with a passivation composition wherein the passivation composition comprises a source of metal ions and a complexing agent;
wherein the surface of the anodized aluminum or anodized aluminum alloy becomes corrosion resistant.
The method according to claim 1 , wherein the complexing agent in the sealing composition is selected from the group consisting of phosphines, phosphonates, acrylic acid polymers, and mixtures thereof.
The method according to claim 2, wherein the complexing agent is in the sealing composition in a concentration from 50 ppm to 500 ppm.
The method according to claim 1, wherein the complexing agent in the passivation composition is selected from the group consisting of phosphines, phosphonates, acrylic acid polymers, and mixtures thereof.
The method according to claim 4, wherein the complexing agent is in the passivation composition in a concentration from 50 ppm to 500 ppm.
The method according to claim 2, wherein the complexing agent in the sealing composition is selected from the group comprising phosphino-carboxylic acid polymers, phosphono-carboxylic acid polymers and mixtures thereof. The method according to claim 6, wherein the complexing agent is 2-phosphonobutane- 1,2,4-tricarboxylic acid.
The method according to claim 4, wherein the complexing agent in the passivation composition is selected from the group comprising phosphino-carboxylic acid polymers, phosphono-carboxylic acid polymers and mixtures thereof.
The method according to claim 8, wherein the complexing agent in the passivation composition is nitrilotrimethylene phosphonic acid.
The method according to claim 1, wherein the aluminum alloy comprises at least 1% silicon.
The method according to claim 10, wherein the aluminum alloy comprises at least 5% silicon.
The method according to claim 1 1, wherein the aluminum alloy comprises at least 7% silicon.
The method according to claim , wherein the metal ions in the passivation composition are selected from the group consisting of tungsten, titanium, molybdenum, vanadium, zirconium, and mixtures thereof.
The method according to claim 13, wherein the metal ions are in the passivation composition at a concentration of between 100 ppm and 3000 ppm
The method according to claim 13, wherein the metal ions in the passivation composition are tungsten.
The method according to claim 13, wherein the metal ions are provided by a metal salt selected from the group consisting of ammonium metatungstate, ammonium molybdate, ammonium tungstate, ammonium vanadate, zirconium acetate, titanium oxalate and mixtures thereof.
The method according to claim 16, wherein the metal salt providing the metal ions is ammonium metatungstate.
The method according to claim 1, wherein the lithium ions are in the sealing composition at a concentration between 300 ppm and 800 ppm.
The method according to claim 1, wherein the fluoride ions are in the sealing
composition at a concentration between 150 ppm and 800 ppm.
The method according to claim 1 , wherein the operating temperature of the sealing composition is between 20°C and 60°C.
The method according to claim 1, wherein the operating temperature of the passivation composition is between 40°C and 80°C.
The method according to claim 1 , wherein the immersion time in the sealing composition is between 0.75 min and 1.25 min per micron of anodized coating on the aluminum alloy surface.
The method according to claim 1 , wherein the pH of the passivation composition is between 5.5 and 7.0
PCT/US2017/067493 2017-01-13 2017-12-20 Sealing anodized aluminum using a low-temperature nickel-free process Ceased WO2018132233A1 (en)

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JP2019536069A JP6811868B2 (en) 2017-01-13 2017-12-20 Sealing of anodized aluminum using a low temperature nickel-free process
CN201780083121.9A CN110168138A (en) 2017-01-13 2017-12-20 Anodised aluminium is closed without nickel technique using low temperature
KR1020197023349A KR102255583B1 (en) 2017-01-13 2017-12-20 Sealing of anodized aluminum using a low temperature nickel-free process
EP17891421.4A EP3545117A4 (en) 2017-01-13 2017-12-20 Sealing anodized aluminum using a low-temperature nickel-free process

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US15/405,417 US10138566B2 (en) 2017-01-13 2017-01-13 Sealing anodized aluminum using a low-temperature nickel-free process

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Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108796579B (en) * 2018-07-20 2021-07-06 江苏飞拓界面工程科技有限公司 Nickel-free hole sealing agent for aluminum anodic oxidation
CN109440163B (en) * 2018-12-28 2022-02-22 江苏飞拓界面工程科技有限公司 Nickel-free hole sealing agent for aluminum and aluminum alloy anodic oxide films and application thereof
CN109972185A (en) * 2019-04-17 2019-07-05 邓华斌 A kind of aluminium alloy is without nickel environmental protection hole sealing agent and preparation method thereof
CN111074323B (en) * 2020-01-19 2021-10-29 南昌航空大学 A kind of aluminum and aluminum alloy anodic oxidation normal temperature nickel-free sealing liquid and sealing method
FR3140382A1 (en) * 2022-10-04 2024-04-05 Safran Landing Systems PROCESS FOR POST-ANODIZATION SEALING OF ALUMINUM AND ALUMINUM ALLOYS WITHOUT USING CHROME

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3175881A (en) * 1962-07-10 1965-03-30 Sylvania Electric Prod Method of producing crystalline ammonium metatungstate
US3900370A (en) * 1972-03-10 1975-08-19 Henkel & Cie Gmbh Process for treating aluminum surfaces
US4220485A (en) * 1978-12-14 1980-09-02 Calgon Corporation Process for sealing phosphatized metal components
US4786336A (en) 1985-03-08 1988-11-22 Amchem Products, Inc. Low temperature seal for anodized aluminum surfaces
US4801360A (en) * 1985-06-19 1989-01-31 Stc Plc Surface treatment of aluminum/silicon alloys
CA2226418A1 (en) 1995-07-07 1997-01-30 Torsten Koerner Process for sealing anodized metals with lithium- and fluoride-containing solutions free from heavy metals
US5775892A (en) * 1995-03-24 1998-07-07 Honda Giken Kogyo Kabushiki Kaisha Process for anodizing aluminum materials and application members thereof
US5935656A (en) * 1995-10-18 1999-08-10 Henkel Kommanditgesellschaft Auf Aktien Short duration hot seal for anodized metal surfaces
US6193815B1 (en) * 1995-06-30 2001-02-27 Henkel Corporation Composition and process for treating the surface of aluminiferous metals
US6447665B1 (en) * 1997-08-22 2002-09-10 Henkel Corporation Faster two-step sealing of anodized aluminum surfaces

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3849264A (en) * 1972-09-05 1974-11-19 Lockheed Aircraft Corp Production of stain resistant, clear, sealed anodized films
US4647347A (en) * 1984-08-16 1987-03-03 Amchen Products, Inc. Process and sealant compositions for sealing anodized aluminum
DE19621818A1 (en) * 1996-05-31 1997-12-04 Henkel Kgaa Short-term hot compression of anodized metal surfaces with solutions containing surfactants
US20020179189A1 (en) * 2001-02-26 2002-12-05 Nelson Homma Process and composition for sealing porous coatings containing metal and oxygen atoms
ES2732264T5 (en) * 2014-02-13 2025-06-26 Doerken Ewald Ag Method for production of a substrate with a chromium vi free and cobalt-free passivation
CN105200493A (en) * 2015-09-24 2015-12-30 马鞍山杰创塑胶科技有限公司 Nickel-free hole sealing agent for bright and smooth aluminum alloy anode oxide film and preparation method of nickel-free hole sealing agent

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3175881A (en) * 1962-07-10 1965-03-30 Sylvania Electric Prod Method of producing crystalline ammonium metatungstate
US3900370A (en) * 1972-03-10 1975-08-19 Henkel & Cie Gmbh Process for treating aluminum surfaces
US4220485A (en) * 1978-12-14 1980-09-02 Calgon Corporation Process for sealing phosphatized metal components
US4786336A (en) 1985-03-08 1988-11-22 Amchem Products, Inc. Low temperature seal for anodized aluminum surfaces
US4801360A (en) * 1985-06-19 1989-01-31 Stc Plc Surface treatment of aluminum/silicon alloys
US5775892A (en) * 1995-03-24 1998-07-07 Honda Giken Kogyo Kabushiki Kaisha Process for anodizing aluminum materials and application members thereof
US6193815B1 (en) * 1995-06-30 2001-02-27 Henkel Corporation Composition and process for treating the surface of aluminiferous metals
CA2226418A1 (en) 1995-07-07 1997-01-30 Torsten Koerner Process for sealing anodized metals with lithium- and fluoride-containing solutions free from heavy metals
US5891269A (en) * 1995-07-07 1999-04-06 Henkel Kommanditgesellschaft Auf Aktien Method of compacting anodized metals with lithium and fluoride-containing solutions without using heavy metals
US5935656A (en) * 1995-10-18 1999-08-10 Henkel Kommanditgesellschaft Auf Aktien Short duration hot seal for anodized metal surfaces
US6447665B1 (en) * 1997-08-22 2002-09-10 Henkel Corporation Faster two-step sealing of anodized aluminum surfaces

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JP2020503460A (en) 2020-01-30
US10138566B2 (en) 2018-11-27
EP3545117A1 (en) 2019-10-02
KR20190100403A (en) 2019-08-28
JP6811868B2 (en) 2021-01-13
CN110168138A (en) 2019-08-23
US20180202061A1 (en) 2018-07-19
KR102255583B1 (en) 2021-05-26

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