US20120241324A1 - Coated article and method for manufacturing same - Google Patents

Coated article and method for manufacturing same Download PDF

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Publication number
US20120241324A1
US20120241324A1 US13/268,173 US201113268173A US2012241324A1 US 20120241324 A1 US20120241324 A1 US 20120241324A1 US 201113268173 A US201113268173 A US 201113268173A US 2012241324 A1 US2012241324 A1 US 2012241324A1
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US
United States
Prior art keywords
anodic oxidation
substrate
oxidation film
coated article
nanopores
Prior art date
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Abandoned
Application number
US13/268,173
Inventor
Hsin-Pei Chang
Wen-Rong Chen
Huann-Wu Chiang
Cheng-Shi Chen
Chao-Yong Zhang
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hongfujin Precision Industry Shenzhen Co Ltd
Hon Hai Precision Industry Co Ltd
Original Assignee
Hongfujin Precision Industry Shenzhen Co Ltd
Hon Hai Precision Industry Co Ltd
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Publication date
Application filed by Hongfujin Precision Industry Shenzhen Co Ltd, Hon Hai Precision Industry Co Ltd filed Critical Hongfujin Precision Industry Shenzhen Co Ltd
Assigned to HON HAI PRECISION INDUSTRY CO., LTD., HONG FU JIN PRECISION INDUSTRY (SHENZHEN) CO., LTD. reassignment HON HAI PRECISION INDUSTRY CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHANG, HSIN-PEI, CHEN, Cheng-shi, CHEN, WEN-RONG, CHIANG, HUANN-WU, ZHANG, Chao-yong
Publication of US20120241324A1 publication Critical patent/US20120241324A1/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/042Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material including a refractory ceramic layer, e.g. refractory metal oxides, ZrO2, rare earth oxides
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/04Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material
    • C23C28/044Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings of inorganic non-metallic material coatings specially adapted for cutting tools or wear applications
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • C25D11/16Pretreatment, e.g. desmutting
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • C25D11/18After-treatment, e.g. pore-sealing
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • C25D11/18After-treatment, e.g. pore-sealing
    • C25D11/24Chemical after-treatment
    • C25D11/243Chemical after-treatment using organic dyestuffs
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25FPROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
    • C25F3/00Electrolytic etching or polishing
    • C25F3/02Etching
    • C25F3/04Etching of light metals

Definitions

  • the disclosure generally relates to coated articles and method for manufacturing the coated articles.
  • PVD physical vapor deposition
  • FIG. 1 illustrates a cross-sectional view of a substrate of an embodiment of a coated article, in which a plurality of nanopores are defined in the substrate.
  • FIG. 2 illustrates a cross-sectional view of an embodiment of a coated article.
  • a coated article 100 includes a substrate 10 , an anodic oxidation film 20 deposited on the substrate 10 and a color layer 30 deposited on the anodic oxidation film 20 .
  • the coated article 100 may be a housing of an electronic device.
  • the substrate 10 may be made of aluminum or aluminum alloy.
  • the substrate 10 includes a porous surface 12 that defines a plurality of nanopores 122 made by electrochemical etching.
  • Each nanopore 122 has a pore opening size between 8 nanometers (nm) and 20 nm in circumference. In this exemplary embodiment, each nanopore 122 has a pore opening size between 10 nm and 15 nm.
  • the anodic oxidation film 20 is formed on the substrate 10 covering the porous surface 12 by anodic oxidation process.
  • the anodic oxidation film 20 has a plurality of bonding protrusions 22 , and each bonding protrusion 22 enters into one of the nanopores 122 so the anodic oxidation film 20 is firmly attached to the substrate 10 by the combination of the bonding protrusions 22 and the nanopores 122 .
  • the anodic oxidation film 20 has a thickness between about 5 micrometers and about 20 micrometers.
  • the color layer 30 is formed on the anodic oxidation film 20 opposite to the substrate 10 by vacuum deposition.
  • the color layer 30 has a thickness between about 0.5 micrometers and about 2 micrometers.
  • the color layer 30 may be a titanium nitride (TiN) layer, a titanium nitric-oxide (TiNO) layer, a titanium carbon-nitride (TiCN) layer, a chromium nitride (CrN) layer or a chromium carbon-nitride (CrCN) layer.
  • a method for manufacturing the coated article 100 may include at least the following steps.
  • the substrate 10 may be made of aluminum or aluminum alloy.
  • Pre-treating the substrate 10 by washing the substrate with a solution (e.g., deionized water or acetone) in an ultrasonic cleaner, to remove impurities, such as grease or dirt.
  • a solution e.g., deionized water or acetone
  • the substrate 10 is dried.
  • the substrate 10 is then treated by alkali treatment in the following way: dipping the substrate 10 in a solution including about 30-50 g/L of NaOH and about 1-2 g/L of sodium gluconate at a temperature of about 40 Celsius degree (° C.)-60° C. for a time of about 1 minute-5 minutes.
  • the substrate 10 is electrochemically etched to form a porous surface 12 with a plurality of nanopores 122 .
  • the substrate 10 acts as an anode
  • a platinum plate acts as cathode, using about 20 g/L-30 g/L of hydrochloric acid or about 250 g/L-350 g/L of sulphuric acid as electrolyte.
  • a constant power having a current density between about 6 A/d m 2 and about 10 A/d m 2 is applied between the anode and the cathode for about 5 minutes to about 10 minutes to form the porous surface 12 .
  • the substrate 10 is treated by anodic oxidation process, to form an anodic oxidation film 20 on the porous surface 12 .
  • Sulphuric acid having about 180 g/L-220 g/L is used as electrolyte.
  • the electrolyte has a temperature between about 19° C. and 21° C.
  • a constant power having a current density between about 1 A/m 2 and about 1.5 A/m 2 is applied to the electrolyte for about 20 minutes to about 40 minutes to form the anodic oxidation film 20 .
  • portions of the anodic oxidation film 20 enter into the nanopores 122 to form a plurality of bonding protrusions 22 . Additionally, each bonding protrusion 22 is retained in one of the nanopores 122 to improve a binding force between the substrate 10 and the anodic oxidation film 20 .
  • the substrate 10 is dipped in an about 5 g/L-10 g/L of nickel acetate solution at a temperature between 90° C. and 100° C. for a time of 10 minutes to 15 minutes, to seal the anodic oxidation film 20 . Therefore, corrosion resistance of the anodic oxidation film 20 is improved.
  • a color layer 30 is deposited on the anodic oxidation film 20 by vacuum deposition, such as vacuum sputtering or vacuum evaporation.
  • the substrate 10 defines a plurality of the nanopores 122
  • the anodic oxidation film 20 includes a plurality of the bonding protrusions 22 .
  • Each bonding protrusion 22 is retained in one of the nanopores 122 so a binding force between the substrate 10 and the anodic oxidation film 20 can be improved.
  • the anodic oxidation film 20 can prevent the coated article from electrochemically etching.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Electrochemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Ceramic Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
  • Laminated Bodies (AREA)
  • Physical Vapour Deposition (AREA)

Abstract

A coated article includes a substrate including a porous surface and an anodic oxidation film. The porous surface defines a plurality of nanopores. The anodic oxidation film is formed on the substrate covering the porous surface by anodic oxidation process. The anodic oxidation film has a plurality of bonding protrusions, and each bonding protrusion is retained in one of the nanopores to improve a binding force between the substrate and the anodic oxidation film.

Description

    BACKGROUND
  • 1. Technical Field
  • The disclosure generally relates to coated articles and method for manufacturing the coated articles.
  • 2. Description of Related Art
  • For improving corrosion resistance of metal, such as aluminum or aluminum alloy, physical vapor deposition (PVD) can be used to deposit a coating on a surface of the metal. However, coatings deposited by PVD typically contain micropores that can allow penetration of contaminants, such as air and moisture, which can corrode the metal.
  • Therefore, there is room for improvement within the art.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • Many aspects of the embodiments can be better understood with reference to the following drawings. The components in the drawings are not necessarily drawn to scale, the emphasis instead being placed upon clearly illustrating the principles of the exemplary coated article and method for manufacturing the coated article. Moreover, in the drawings like reference numerals designate corresponding parts throughout the several views. Wherever possible, the same reference numbers are used throughout the drawings to refer to the same or like elements of an embodiment.
  • FIG. 1 illustrates a cross-sectional view of a substrate of an embodiment of a coated article, in which a plurality of nanopores are defined in the substrate.
  • FIG. 2 illustrates a cross-sectional view of an embodiment of a coated article.
  • DETAILED DESCRIPTION
  • Referring to FIGS. 1 and 2, a coated article 100 includes a substrate 10, an anodic oxidation film 20 deposited on the substrate 10 and a color layer 30 deposited on the anodic oxidation film 20. The coated article 100 may be a housing of an electronic device.
  • The substrate 10 may be made of aluminum or aluminum alloy. The substrate 10 includes a porous surface 12 that defines a plurality of nanopores 122 made by electrochemical etching. Each nanopore 122 has a pore opening size between 8 nanometers (nm) and 20 nm in circumference. In this exemplary embodiment, each nanopore 122 has a pore opening size between 10 nm and 15 nm.
  • The anodic oxidation film 20 is formed on the substrate 10 covering the porous surface 12 by anodic oxidation process. The anodic oxidation film 20 has a plurality of bonding protrusions 22, and each bonding protrusion 22 enters into one of the nanopores 122 so the anodic oxidation film 20 is firmly attached to the substrate 10 by the combination of the bonding protrusions 22 and the nanopores 122. The anodic oxidation film 20 has a thickness between about 5 micrometers and about 20 micrometers.
  • The color layer 30 is formed on the anodic oxidation film 20 opposite to the substrate 10 by vacuum deposition. The color layer 30 has a thickness between about 0.5 micrometers and about 2 micrometers. The color layer 30 may be a titanium nitride (TiN) layer, a titanium nitric-oxide (TiNO) layer, a titanium carbon-nitride (TiCN) layer, a chromium nitride (CrN) layer or a chromium carbon-nitride (CrCN) layer.
  • A method for manufacturing the coated article 100 may include at least the following steps.
  • Providing a substrate 10. The substrate 10 may be made of aluminum or aluminum alloy.
  • Pre-treating the substrate 10 by washing the substrate with a solution (e.g., deionized water or acetone) in an ultrasonic cleaner, to remove impurities, such as grease or dirt. The substrate 10 is dried. The substrate 10 is then treated by alkali treatment in the following way: dipping the substrate 10 in a solution including about 30-50 g/L of NaOH and about 1-2 g/L of sodium gluconate at a temperature of about 40 Celsius degree (° C.)-60° C. for a time of about 1 minute-5 minutes.
  • The substrate 10 is electrochemically etched to form a porous surface 12 with a plurality of nanopores 122. During electrochemical etching, the substrate 10 acts as an anode, a platinum plate acts as cathode, using about 20 g/L-30 g/L of hydrochloric acid or about 250 g/L-350 g/L of sulphuric acid as electrolyte. A constant power having a current density between about 6 A/d m2 and about 10 A/d m2 is applied between the anode and the cathode for about 5 minutes to about 10 minutes to form the porous surface 12.
  • The substrate 10 is treated by anodic oxidation process, to form an anodic oxidation film 20 on the porous surface 12. Sulphuric acid having about 180 g/L-220 g/L is used as electrolyte. The electrolyte has a temperature between about 19° C. and 21° C. A constant power having a current density between about 1 A/m2 and about 1.5 A/m2 is applied to the electrolyte for about 20 minutes to about 40 minutes to form the anodic oxidation film 20. During depositing the anodic oxidation film 20, portions of the anodic oxidation film 20 enter into the nanopores 122 to form a plurality of bonding protrusions 22. Additionally, each bonding protrusion 22 is retained in one of the nanopores 122 to improve a binding force between the substrate 10 and the anodic oxidation film 20.
  • The substrate 10 is dipped in an about 5 g/L-10 g/L of nickel acetate solution at a temperature between 90° C. and 100° C. for a time of 10 minutes to 15 minutes, to seal the anodic oxidation film 20. Therefore, corrosion resistance of the anodic oxidation film 20 is improved.
  • A color layer 30 is deposited on the anodic oxidation film 20 by vacuum deposition, such as vacuum sputtering or vacuum evaporation.
  • In above exemplary, the substrate 10 defines a plurality of the nanopores 122, the anodic oxidation film 20 includes a plurality of the bonding protrusions 22. Each bonding protrusion 22 is retained in one of the nanopores 122 so a binding force between the substrate 10 and the anodic oxidation film 20 can be improved. Additionally, the anodic oxidation film 20 can prevent the coated article from electrochemically etching.
  • It is to be understood, however, that even through numerous characteristics and advantages of the exemplary disclosure have been set forth in the foregoing description, together with details of the system and function of the disclosure, the disclosure is illustrative only, and changes may be made in detail, especially in matters of shape, size, and arrangement of parts within the principles of the disclosure to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.

Claims (18)

1. A coated article, comprising:
a substrate including a porous surface, the porous surface defining a plurality of nanopores; and
an anodic oxidation film formed on the substrate covering the porous surface by anodic oxidation process;
wherein the anodic oxidation film has a plurality of bonding protrusions, and each bonding protrusion is retained in a nanopore to improve a binding force between the substrate and the anodic oxidation film.
2. The coated article as claimed in claim 1, wherein the substrate is made of aluminum or aluminum alloy.
3. The coated article as claimed in claim 1, wherein the nanopores are formed by electrochemical etching.
4. The coated article as claimed in claim 1, wherein each nanopore has a pore opening size between 8 nm and 20 nm in circumference.
5. The coated article as claimed in claim 1, wherein each nanopore has a pore opening size between 10 nm and 15 nm in circumference.
6. The coated article as claimed in claim 1, wherein the anodic oxidation film has a thickness between about 5 micrometers and about 20 micrometers.
7. The coated article as claimed in claim 1, further comprising a color layer formed on the anodic oxidation film opposite to the substrate.
8. The coated article as claimed in claim 7, wherein the color layer has a thickness between about 0.5 micrometers and about 2 micrometers.
9. The coated article as claimed in claim 7, wherein the color layer is one selecting from a group consisting of a titanium nitride layer, a titanium nitric-oxide layer, a titanium carbon-nitride layer, a chromium nitride layer and a chromium carbon-nitride layer.
10. A method for manufacturing a coated article, the method comprising:
providing a substrate, the substrate including a porous surface, the porous surface defining a plurality of nanopores;
forming an anodic oxidation film on the substrate covering the porous surface by anodic oxidation process;
during forming the anodic oxidation film, portions of the anodic oxidation film enter into the nanopores to form a plurality of bonding protrusions, and each bonding protrusion is retained in one of the nanopores to improve a binding force between the substrate and the anodic oxidation film.
11. The method of claim 10, wherein the substrate is made of aluminum or aluminum alloy.
12. The method of claim 10, wherein before the anodic oxidation film is deposited on the substrate, the substrate is treated by alkali treatment.
13. The method of claim 12, wherein during the substrate is treated by alkali treatment, the substrate is dipped in a solution including 30-50 g/L of NaOH and 1-2 g/L of sodium gluconate at a temperature of 40-60° C. for a time of 1-5 minutes.
14. The method of claim 10, wherein the nanopores are defined by electrochemical etching.
15. The method of claim 14, wherein during electrochemical etching, the substrate acts as an anode, a platinum plate acts as cathode, using 20-30 g/L of hydrochloric acid or 250-350 g/L of sulphuric acid as electrolyte, a constant power applied between the anode and the cathode have a current density between about 6 A/d m2 and about 10 A/d m2 for about 5 minutes to about 10 minutes to define the nanopores.
16. The method of claim 10, wherein during anodic oxidation, using 180-220 g/L of sulphuric acid as electrolyte, the electrolyte has a temperature between 19° C. and 21° C., a constant power applied to the electrolyte has a current density between about 1 A/m2 and about 1.5 A/m2 for about 20 minutes to about 40 minutes to form the anodic oxidation film.
17. The method of claim 10, wherein after depositing the anodic oxidation film, the substrate is dipped in a 5-10 g/L of nickel acetate solution at a temperature between 90° C. and 100° C. for a time of 10 minutes to 15 minutes, to improve corrosion resistance of the anodic oxidation film.
18. The method of claim 10, further comprising a step of depositing a color layer on the anodic oxidation film by vacuum deposition.
US13/268,173 2011-03-24 2011-10-07 Coated article and method for manufacturing same Abandoned US20120241324A1 (en)

Applications Claiming Priority (2)

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CN201110072038.6A CN102691080B (en) 2011-03-24 2011-03-24 Aluminum products
CN201110072038.6 2011-03-24

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