EP1233084A2 - "Anodizing process, with low environmental impact, for a workpiece of aluminium or aluminium alloys" - Google Patents

"Anodizing process, with low environmental impact, for a workpiece of aluminium or aluminium alloys" Download PDF

Info

Publication number
EP1233084A2
EP1233084A2 EP02003522A EP02003522A EP1233084A2 EP 1233084 A2 EP1233084 A2 EP 1233084A2 EP 02003522 A EP02003522 A EP 02003522A EP 02003522 A EP02003522 A EP 02003522A EP 1233084 A2 EP1233084 A2 EP 1233084A2
Authority
EP
European Patent Office
Prior art keywords
workpiece
aluminium
process according
anodizing
minutes
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP02003522A
Other languages
German (de)
French (fr)
Other versions
EP1233084A3 (en
Inventor
Alessandro Dattilo
Salvatore Tamiro
Carlo Romano
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.)
Alenia Aermacchi SpA
Original Assignee
Alenia Aeronautica SpA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Alenia Aeronautica SpA filed Critical Alenia Aeronautica SpA
Publication of EP1233084A2 publication Critical patent/EP1233084A2/en
Publication of EP1233084A3 publication Critical patent/EP1233084A3/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C25D11/06Anodisation of aluminium or alloys based thereon characterised by the electrolytes used

Definitions

  • the present invention relates to an anodizing process for a workpiece (such as, for example, a part or a component of a system) of aluminium or aluminium alloys, this definition being intended to comprise pure or almost pure aluminium, as well as combinations thereof in all percentages with other elements.
  • a workpiece such as, for example, a part or a component of a system
  • aluminium or aluminium alloys this definition being intended to comprise pure or almost pure aluminium, as well as combinations thereof in all percentages with other elements.
  • this process makes use of the above-mentioned workpiece as the anode of an electrolytic cell in the presence of an aqueous acid solution in order to form on the surface of the workpiece a coating of aluminium oxide.
  • This coating results in better properties concerning the resistance to corrosion and the adhesion of paints, bonding agents and other organic coatings suitable for improving the appearance or the resistance to corrosion of the finished workpiece.
  • this acid solution substantially comprises sulphuric acid at high concentrations or chromic acid, the latter being the compound mainly used in the field of aeronautics.
  • the problem addressed by the present invention is to provide an anodizing process having a lesser toxicological impact on the environment in comparison with the known types, avoiding the use of chromic acid whilst nevertheless obtaining anodized workpieces having properties which are at least equivalent to those of workpieces obtained by conventional means.
  • aqueous acid solution contains from 10 to 200 g sulphuric acid and from 5 to 200 g L(+)-tartaric acid per litre of solution.
  • the process according to the invention has the advantage of eliminating, or in any case greatly reducing, the production of industrial waste, in particular waste containing compounds of chromium, without causing the formation of other waste materials having particular toxic or dangerous properties.
  • the process according to the invention further has the advantage of having a cycle time which is approximately 40% short of that of the analogous process which makes use of chromic acid, producing anodized workpieces having properties at least equivalent if not superior. Consequently, the process according to the invention allows a considerable reduction in running costs to be obtained in that it results in lower costs for the treatment of the waste and involves a substantially lower rate of consumption for the different chemicals used for replenishing the baths, which have an operational life greater than those used in known processes.
  • the aqueous acid solution of the process according to the invention preferably contains from 20 to 80 g sulphuric acid and from 30 to 120 g L(+)-tartaric acid per litre of solution.
  • the aqueous solution is maintained, during the anodizing treatment, at a temperature of between ambient temperature and 120°C and, more preferably, between 25 and 35°C.
  • the electrolytic cell in which the process according to the invention is carried out, is preferably subjected to a voltage of between 1 and 120 V and, more preferably, of between 10 and 30 V.
  • the process according to the invention advantageously has a duration of between 5 and 120 minutes and, preferably, of between 5 and 30 minutes.
  • the anodizing process is generally preceded by a cleaning and/or deoxidizing treatment of the workpiece to be anodized and can be followed by a sealing treatment and, optionally, rinsing for the anodized workpiece.
  • these treatments are of conventional type and completely compatible with the present invention and can be selected at will from treatments known to this end by the person skilled in the art.
  • the workpiece advantageously has, upon completion of the anodizing treatment, an oxidized surface coating having a thickness of between a few micrometres and several tens of micrometres.
  • a workpiece (of a 2000-series aluminium alloy having dimensions of 150x100x1 mm) was first subjected in a conventional manner to cleaning and deoxidizing treatments, such as degreasing by immersion for approximately 10 minutes, rinsing by immersion in drinking water for approximately 3 minutes, pickling/deoxidation by immersion for approximately 10 minutes and rinsing by immersion in drinking water, preferably followed by further rinsing by immersion in deionized water for a total of approximately 3 minutes.
  • the workpiece was then used as the anode of an electrochemical cell, in which the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 45 g sulphuric acid and 80 g L(+)-tartaric acid per litre of solution and was maintained at a temperature of between 30 and 35°C. The workpiece was kept completely immersed in the acid solution.
  • the electrical voltage was increased from an initial value of 0 V to a value of 18 V at a rate in the order of 3.6 V/min.
  • the final voltage value was maintained for 25 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 5 ⁇ m.
  • the anodized workpiece was then subjected to treatments which.are conventional per se, such as rinsing with drinking water, preferably followed by further rinsing with deionized water for an overall immersion time of approximately 3 minutes and sealing by immersion for approximately 45 minutes.
  • treatments which.are conventional per se, such as rinsing with drinking water, preferably followed by further rinsing with deionized water for an overall immersion time of approximately 3 minutes and sealing by immersion for approximately 45 minutes.
  • the workpiece was then dried with air, in particular at a low temperature, if good properties of adhesiveness were required for the oxide.
  • a workpiece (of a 7000-series aluminium alloy having dimensions of 150x100x1 mm) was first subjected in a conventional manner to cleaning and deoxidizing treatments, similar to those described with reference to Example 1.
  • the workpiece was then used as the anode of an electrochemical cell, in which the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 45 g sulphuric acid and 80 g L(+)-tartaric acid per litre of solution and was maintained at a temperature of between 30 and 35°C. The workpiece was kept completely immersed in the acid solution.
  • the electrical voltage was increased from an initial value of 0 V to a value of 15 V at a rate in the order of 3 V/min.
  • the final voltage value was maintained for 25 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 5 ⁇ m.
  • the anodized workpiece was then subjected to rinsing and sealing treatments, which are conventional per se, similar to those described with reference to Example 1.
  • a workpiece (of a plated aluminium alloy or pure aluminium having dimensions of 150x100x1 mm) was first subjected, in a conventional manner, to cleaning and deoxidizing treatments, similar to those described with reference to Example 1.
  • the workpiece was then used as the anode of an electrochemical cell, in which.the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 45 g sulphuric acid and 80 g L(+)-tartaric acid per litre of solution and was maintained at a temperature of between 30 and 35°C. The workpiece was kept completely immersed in the acid solution.
  • the electrical voltage was increased from an initial value of 0 V to a value of 15 V at a rate in the order of 3 V/min.
  • the final voltage value was maintained for 25 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 5 ⁇ m.
  • the anodized workpiece was then subjected to rinsing and sealing treatments, which are conventional per se, similar to those described with reference to Example 1.
  • a workpiece (of a plated aluminium alloy or a pure aluminium having dimensions of 150x100x1 mm) was first subjected in a conventional manner to cleaning and deoxidizing treatments, similar to those described with reference to Example 1.
  • the workpiece was then used as the anode of an electrochemical cell, in which the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 65 g chromic acid and was maintained at a temperature of between 35 and 40°C.
  • the workpiece was kept completely immersed in the acid solution.
  • the electrical voltage was increased from an initial value of 0 V to a value of 40 V at a rate in the order of 5 V/min.
  • the final voltage value was maintained for 45 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 3 ⁇ m.
  • the anodized workpiece was then subjected to rinsing and sealing treatments, which are conventional per se, similar to those described with reference to Example 1.
  • a comparison of the results of the tests carried out on the workpieces of the Examples according to the invention and the Example for comparative purposes establishes that the process according to the invention produces oxides having properties which are superior to those of the oxides obtained with conventional processes. Furthermore, the process according to the invention offers environmental advantages associated with the different types of product used, and has a duration which is substantially shorter.
  • aqueous acid solution could contain, in addition to sulphuric acid and tartaric acid, any other components or combinations of components which are compatible with those substances.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)
  • Catalysts (AREA)

Abstract

The process for anodizing a workpiece of aluminium or aluminium alloys provides for the use of the workpiece as the anode of an electrolytic cell in the presence of an aqueous acid solution which contains from 10 to 200 g sulphuric acid and from 5 to 200 g L(+)-tartaric acid.

Description

  • The present invention relates to an anodizing process for a workpiece (such as, for example, a part or a component of a system) of aluminium or aluminium alloys, this definition being intended to comprise pure or almost pure aluminium, as well as combinations thereof in all percentages with other elements.
  • In greater detail, this process makes use of the above-mentioned workpiece as the anode of an electrolytic cell in the presence of an aqueous acid solution in order to form on the surface of the workpiece a coating of aluminium oxide.
  • This coating results in better properties concerning the resistance to corrosion and the adhesion of paints, bonding agents and other organic coatings suitable for improving the appearance or the resistance to corrosion of the finished workpiece.
  • Conventionally, this acid solution substantially comprises sulphuric acid at high concentrations or chromic acid, the latter being the compound mainly used in the field of aeronautics.
  • The problem addressed by the present invention is to provide an anodizing process having a lesser toxicological impact on the environment in comparison with the known types, avoiding the use of chromic acid whilst nevertheless obtaining anodized workpieces having properties which are at least equivalent to those of workpieces obtained by conventional means.
  • This problem is solved according to the invention by an anodizing process of the type indicated in the introduction to the present description and characterized in that the aqueous acid solution contains from 10 to 200 g sulphuric acid and from 5 to 200 g L(+)-tartaric acid per litre of solution.
  • The process according to the invention has the advantage of eliminating, or in any case greatly reducing, the production of industrial waste, in particular waste containing compounds of chromium, without causing the formation of other waste materials having particular toxic or dangerous properties.
  • The process according to the invention further has the advantage of having a cycle time which is approximately 40% short of that of the analogous process which makes use of chromic acid, producing anodized workpieces having properties at least equivalent if not superior. Consequently, the process according to the invention allows a considerable reduction in running costs to be obtained in that it results in lower costs for the treatment of the waste and involves a substantially lower rate of consumption for the different chemicals used for replenishing the baths, which have an operational life greater than those used in known processes.
  • The aqueous acid solution of the process according to the invention preferably contains from 20 to 80 g sulphuric acid and from 30 to 120 g L(+)-tartaric acid per litre of solution.
  • Again preferably, the aqueous solution is maintained, during the anodizing treatment, at a temperature of between ambient temperature and 120°C and, more preferably, between 25 and 35°C.
  • The electrolytic cell, in which the process according to the invention is carried out, is preferably subjected to a voltage of between 1 and 120 V and, more preferably, of between 10 and 30 V.
  • The process according to the invention advantageously has a duration of between 5 and 120 minutes and, preferably, of between 5 and 30 minutes.
  • The anodizing process is generally preceded by a cleaning and/or deoxidizing treatment of the workpiece to be anodized and can be followed by a sealing treatment and, optionally, rinsing for the anodized workpiece. In principle, these treatments are of conventional type and completely compatible with the present invention and can be selected at will from treatments known to this end by the person skilled in the art.
  • The workpiece advantageously has, upon completion of the anodizing treatment, an oxidized surface coating having a thickness of between a few micrometres and several tens of micrometres.
  • There now follow, merely by way of non-limiting, illustrative example, examples of the anodizing process according to the invention, as well as a comparative example performed by conventional techniques.
  • EXAMPLE 1 Anodizing a 2000-series aluminium alloy with sulphuric-tartaric acid
  • A workpiece (of a 2000-series aluminium alloy having dimensions of 150x100x1 mm) was first subjected in a conventional manner to cleaning and deoxidizing treatments, such as degreasing by immersion for approximately 10 minutes, rinsing by immersion in drinking water for approximately 3 minutes, pickling/deoxidation by immersion for approximately 10 minutes and rinsing by immersion in drinking water, preferably followed by further rinsing by immersion in deionized water for a total of approximately 3 minutes.
  • The workpiece was then used as the anode of an electrochemical cell, in which the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 45 g sulphuric acid and 80 g L(+)-tartaric acid per litre of solution and was maintained at a temperature of between 30 and 35°C. The workpiece was kept completely immersed in the acid solution.
  • The electrical voltage was increased from an initial value of 0 V to a value of 18 V at a rate in the order of 3.6 V/min. The final voltage value was maintained for 25 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 5 µm.
  • The anodized workpiece was then subjected to treatments which.are conventional per se, such as rinsing with drinking water, preferably followed by further rinsing with deionized water for an overall immersion time of approximately 3 minutes and sealing by immersion for approximately 45 minutes. The workpiece was then dried with air, in particular at a low temperature, if good properties of adhesiveness were required for the oxide.
  • The properties of this oxide are indicated in Table I.
  • EXAMPLE 2 Anodizing a 7000-series aluminium alloy with sulphuric-tartaric acid
  • A workpiece (of a 7000-series aluminium alloy having dimensions of 150x100x1 mm) was first subjected in a conventional manner to cleaning and deoxidizing treatments, similar to those described with reference to Example 1.
  • The workpiece was then used as the anode of an electrochemical cell, in which the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 45 g sulphuric acid and 80 g L(+)-tartaric acid per litre of solution and was maintained at a temperature of between 30 and 35°C. The workpiece was kept completely immersed in the acid solution.
  • The electrical voltage was increased from an initial value of 0 V to a value of 15 V at a rate in the order of 3 V/min. The final voltage value was maintained for 25 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 5 µm.
  • The anodized workpiece was then subjected to rinsing and sealing treatments, which are conventional per se, similar to those described with reference to Example 1.
  • The properties of the oxide coating obtained are indicated in Table I.
  • EXAMPLE 3 Anodizing plated or pure aluminium with sulphuric-tartaric acid
  • A workpiece (of a plated aluminium alloy or pure aluminium having dimensions of 150x100x1 mm) was first subjected, in a conventional manner, to cleaning and deoxidizing treatments, similar to those described with reference to Example 1.
  • The workpiece was then used as the anode of an electrochemical cell, in which.the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 45 g sulphuric acid and 80 g L(+)-tartaric acid per litre of solution and was maintained at a temperature of between 30 and 35°C. The workpiece was kept completely immersed in the acid solution.
  • The electrical voltage was increased from an initial value of 0 V to a value of 15 V at a rate in the order of 3 V/min. The final voltage value was maintained for 25 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 5 µm.
  • The anodized workpiece was then subjected to rinsing and sealing treatments, which are conventional per se, similar to those described with reference to Example 1.
  • The properties of the oxide coating obtained are indicated in Table I.
  • EXAMPLE 4 (for comparative purposes) Anodizing with chromic acid
  • A workpiece (of a plated aluminium alloy or a pure aluminium having dimensions of 150x100x1 mm) was first subjected in a conventional manner to cleaning and deoxidizing treatments, similar to those described with reference to Example 1.
  • The workpiece was then used as the anode of an electrochemical cell, in which the cathode was constituted by corrosion-resistant steel of the type AISI 321 and having a surface area equal to or greater than that to be oxidized and in the presence of an aqueous acid solution containing 65 g chromic acid and was maintained at a temperature of between 35 and 40°C. The workpiece was kept completely immersed in the acid solution.
  • The electrical voltage was increased from an initial value of 0 V to a value of 40 V at a rate in the order of 5 V/min. The final voltage value was maintained for 45 minutes, producing on the workpiece, upon completion of the anodizing treatment, an oxidized coating having a thickness of approximately 3 µm.
  • The anodized workpiece was then subjected to rinsing and sealing treatments, which are conventional per se, similar to those described with reference to Example 1.
  • The properties of the oxide coating obtained are indicated in Table I.
    Figure 00080001
  • A comparison of the results of the tests carried out on the workpieces of the Examples according to the invention and the Example for comparative purposes establishes that the process according to the invention produces oxides having properties which are superior to those of the oxides obtained with conventional processes. Furthermore, the process according to the invention offers environmental advantages associated with the different types of product used, and has a duration which is substantially shorter.
  • Of course, without altering the principle of the invention, the details of implementation and the embodiments can vary extensively in relation to the description, which is given purely by way of example, without in any way departing from the scope thereof. In particular, the aqueous acid solution could contain, in addition to sulphuric acid and tartaric acid, any other components or combinations of components which are compatible with those substances.

Claims (7)

  1. Process for anodizing a workpiece of aluminium or aluminium alloys, which provides for the use of the workpiece as the anode of an electrolytic cell in the presence of an aqueous acid solution,
    the process being characterized in that the aqueous acid solution contains from 10 to 200 g sulphuric acid and from 5 to 200 g L(+)-tartaric acid.
  2. Process according to claim 1, characterized in that the aqueous acid solution contains from 20 to 80 g sulphuric acid and from 30 to 120 g L(+)-tartaric acid per litre of solution.
  3. Process according to either of the preceding claims, characterized in that the solution is maintained, during the anodizing treatment, at a temperature of between ambient temperature and 120°C, and preferably between 25 and 35°C.
  4. Process according to any one of the preceding claims, characterized in that the electrolytic cell is subjected to a voltage of between 1 and 120 V, and preferably of between 10 and 30 V.
  5. Process according to any one of the preceding claims, characterized in that it has a duration of between 5 and 120 minutes, and preferably of between 5 and 30 minutes.
  6. Process according to any one of the preceding claims, characterized in that it is preceded by a cleaning, deoxidizing and rinsing treatment for the workpiece to be anodized.
  7. Process according to any one of the preceding claims, characterized in that it is followed by a rinsing and sealing treatment for the anodized workpiece.
EP02003522A 2001-02-20 2002-02-15 "Anodizing process, with low environmental impact, for a workpiece of aluminium or aluminium alloys" Withdrawn EP1233084A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITTO010149 2001-02-20
IT2001TO000149A ITTO20010149A1 (en) 2001-02-20 2001-02-20 LOW ECOLOGICAL ANODIZATION PROCEDURE OF A PIECE OF ALUMINUM OR ALUMINUM ALLOYS.

Publications (2)

Publication Number Publication Date
EP1233084A2 true EP1233084A2 (en) 2002-08-21
EP1233084A3 EP1233084A3 (en) 2004-03-31

Family

ID=11458586

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02003522A Withdrawn EP1233084A3 (en) 2001-02-20 2002-02-15 "Anodizing process, with low environmental impact, for a workpiece of aluminium or aluminium alloys"

Country Status (3)

Country Link
US (1) US20020157961A1 (en)
EP (1) EP1233084A3 (en)
IT (1) ITTO20010149A1 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357206A2 (en) * 2002-04-22 2003-10-29 Messier-Bugatti Anodisation process of an aluminium alloy element
WO2004027121A2 (en) * 2002-09-17 2004-04-01 The Boeing Company Accelerated sulfuric acid and boric sulfuric acid anodize process
DE10361888B3 (en) * 2003-12-23 2005-09-22 Airbus Deutschland Gmbh Anodizing process for aluminum materials
DE102008008055B3 (en) * 2008-02-08 2009-08-06 Airbus Deutschland Gmbh Method for applying a multifunctional coating on aluminum parts and coated workpiece
ES2324850A1 (en) * 2007-10-29 2009-08-17 Airbus España, S.L. Procedure for anodising aluminium or aluminium alloys
US7771578B2 (en) 2004-05-04 2010-08-10 Mtu Aero Engines Gmbh Method for producing of a galvanic coating
CN111112943A (en) * 2018-10-31 2020-05-08 江苏瑞尔隆鼎实业有限公司 Method for machining ABS/ESC valve body for automobile braking system
EP4269662A1 (en) 2022-04-29 2023-11-01 Airbus Operations GmbH Methods for anodizing a part surface and subsequently coating the anodized part surface for corrosion protection purposes

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070267299A1 (en) * 2003-01-30 2007-11-22 Yoshiyuki Mitani Method for Forming Anodic Oxide Layer on Surface of Aluminum or Aluminum Alloy
US7527872B2 (en) * 2005-10-25 2009-05-05 Goodrich Corporation Treated aluminum article and method for making same
FR2992979B1 (en) * 2012-07-04 2014-08-08 Messier Bugatti Dowty PROCESSING PROCESS WITH ANODIZATION OF ALUMINUM ALLOYS CONTAINING COPPER
US10094037B2 (en) 2014-10-13 2018-10-09 United Technologies Corporation Hierarchically structured duplex anodized aluminum alloy
EP3247823A1 (en) * 2015-01-19 2017-11-29 Council of Scientific & Industrial Research A process for the preparation of corrosion resistant sealed anodized coatings on aluminum alloy
US20200024766A1 (en) * 2018-07-18 2020-01-23 Leonardo S.P.A. Anodization method for corrosion protection of aluminium alloy elements used in an aircraft structure

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH447758A (en) * 1965-09-30 1967-11-30 Alusuisse Process and device for anodic oxidation of aluminum and its alloys
US3382160A (en) * 1960-03-31 1968-05-07 Asada Tahei Process for inorganically coloring aluminum
EP0065421A1 (en) * 1981-05-19 1982-11-24 Sankyo Aluminium Industry Company Limited Method of treating a surface of an aluminum to form a pattern thereon

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS547267B2 (en) * 1973-09-21 1979-04-05
ES490784A0 (en) * 1980-04-22 1981-02-16 Empresa Nacional Aluminio PROCESS TO ELECTROLYTICALLY COLOR ALUMINUM AND ITS ALLOYS
CN1004887B (en) * 1985-12-16 1989-07-26 青海省太阳能研究所 Fast anodic oxidation technique of aluminum film under room temp.
DE3616725A1 (en) * 1986-05-14 1987-11-19 Alusuisse Manufacture of aluminium alloy products having a uniformly grey, light-fast surface
CN1106865A (en) * 1994-02-04 1995-08-16 大连星光电磁铁厂 Aluminium foil anodic oxidation electrolyte solution for electric appliance

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3382160A (en) * 1960-03-31 1968-05-07 Asada Tahei Process for inorganically coloring aluminum
CH447758A (en) * 1965-09-30 1967-11-30 Alusuisse Process and device for anodic oxidation of aluminum and its alloys
EP0065421A1 (en) * 1981-05-19 1982-11-24 Sankyo Aluminium Industry Company Limited Method of treating a surface of an aluminum to form a pattern thereon

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE CA [Online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; FANG, JINGZHONG ET AL: "Rapid anodic oxidation of aluminum at room temperature" retrieved from STN Database accession no. 109:82073 CA XP002267533 & CN 1 004 887 B (QINGHAI PROVINCIAL SOLAR ENERGY INSTITUTE, PEOP. REP. CHINA) 26 July 1989 (1989-07-26) *
DATABASE WPI Section Ch, Week 199731 Derwent Publications Ltd., London, GB; Class A97, AN 1997-333590 XP002267534 & CN 1 106 865 A (XINGGUANG ELECTROMAGNET FACTORY DALIAN), 16 August 1995 (1995-08-16) *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357206A2 (en) * 2002-04-22 2003-10-29 Messier-Bugatti Anodisation process of an aluminium alloy element
EP1357206A3 (en) * 2002-04-22 2004-05-12 Messier-Bugatti Anodisation process of an aluminium alloy element
WO2004027121A2 (en) * 2002-09-17 2004-04-01 The Boeing Company Accelerated sulfuric acid and boric sulfuric acid anodize process
WO2004027121A3 (en) * 2002-09-17 2004-05-21 Boeing Co Accelerated sulfuric acid and boric sulfuric acid anodize process
DE10361888B3 (en) * 2003-12-23 2005-09-22 Airbus Deutschland Gmbh Anodizing process for aluminum materials
US7771578B2 (en) 2004-05-04 2010-08-10 Mtu Aero Engines Gmbh Method for producing of a galvanic coating
ES2324850A1 (en) * 2007-10-29 2009-08-17 Airbus España, S.L. Procedure for anodising aluminium or aluminium alloys
EA015400B1 (en) * 2007-10-29 2011-08-30 Эрбус Оперейшнс, С.Л. Procedure for anodising aluminium or aluminium alloys
WO2009098099A3 (en) * 2008-02-08 2010-01-21 Airbus Operations Gmbh Multifunctional coating of aluminium pieces
DE102008008055B3 (en) * 2008-02-08 2009-08-06 Airbus Deutschland Gmbh Method for applying a multifunctional coating on aluminum parts and coated workpiece
US9334577B2 (en) 2008-02-08 2016-05-10 Airbus Operations Gmbh Multifunctional coating of aluminium pieces
CN111112943A (en) * 2018-10-31 2020-05-08 江苏瑞尔隆鼎实业有限公司 Method for machining ABS/ESC valve body for automobile braking system
CN111112943B (en) * 2018-10-31 2022-04-15 江苏瑞尔隆鼎实业有限公司 Method for machining ABS/ESC valve body for automobile braking system
EP4269662A1 (en) 2022-04-29 2023-11-01 Airbus Operations GmbH Methods for anodizing a part surface and subsequently coating the anodized part surface for corrosion protection purposes

Also Published As

Publication number Publication date
US20020157961A1 (en) 2002-10-31
EP1233084A3 (en) 2004-03-31
ITTO20010149A1 (en) 2002-08-20
ITTO20010149A0 (en) 2001-02-20

Similar Documents

Publication Publication Date Title
CN104831332B (en) A kind of method that steel surface directly generates the anti-corrosion differential arc oxidation film layer of black
EP1233084A2 (en) "Anodizing process, with low environmental impact, for a workpiece of aluminium or aluminium alloys"
EP0904427B1 (en) Galvanized aluminium sheet
JPH04297595A (en) Method of zinc electroplating on aluminum strip
KR101977807B1 (en) Method for anodizing surface treatment of automotive sunroof rails
EP0264972A1 (en) Method of cleaning aluminium surfaces
US20230398571A1 (en) Corrosion-resistant magnesium alloy with a multi-level protective coating and preparation process thereof
JP4862445B2 (en) Method for producing electrogalvanized steel sheet
US4455201A (en) Bath and method for anodizing aluminized parts
JPS60125395A (en) Zn-alumina composite electroplated steel sheet having high corrosion resistance
US3275537A (en) Process of anodizing aluminum
JP3916222B2 (en) Surface treatment method of magnesium alloy
JP7400766B2 (en) Zinc-based electroplated steel sheet and its manufacturing method
JP3746212B2 (en) Method of processing magnesium alloy members for press forming
KR100226274B1 (en) Two-step chemical/electrochemical process for coating magnesium
KR101803434B1 (en) Desmut composition for aluminium material
JPH041079B2 (en)
JP2000226690A (en) Production of surface treated metallic sheet for coating substrate and surface treated metallic sheet for coating substrate
JP2003155595A (en) Anodizing method of aluminium and aluminium alloy
JPH07173684A (en) Surface treatment of metallic aluminum material
JPH0827595A (en) Surface treatment of aluminum alloy sheet for can end
JPH08100290A (en) Treatment of adhesive substrate of anodic oxide film forming aluminum
JP2010180474A (en) Method for producing chemically converted product
JP2004091911A (en) Anodizing treatment liquid for magnesium or magnesium alloy
JPH0699838B2 (en) Method for producing Zn or Zn-Ni alloy plated stainless steel strip

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

AKX Designation fees paid
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

REG Reference to a national code

Ref country code: DE

Ref legal event code: 8566

18D Application deemed to be withdrawn

Effective date: 20040831