US2288995A - Surface treatment of magnesium and its alloys - Google Patents

Surface treatment of magnesium and its alloys Download PDF

Info

Publication number
US2288995A
US2288995A US329533A US32953340A US2288995A US 2288995 A US2288995 A US 2288995A US 329533 A US329533 A US 329533A US 32953340 A US32953340 A US 32953340A US 2288995 A US2288995 A US 2288995A
Authority
US
United States
Prior art keywords
magnesium
acid
article
solution
alloys
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.)
Expired - Lifetime
Application number
US329533A
Inventor
Long Herbert K De
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.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Dow Chemical Co filed Critical Dow Chemical Co
Priority to US329533A priority Critical patent/US2288995A/en
Application granted granted Critical
Publication of US2288995A publication Critical patent/US2288995A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C23C22/00Chemical 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
    • C23C22/05Chemical 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
    • C23C22/06Chemical 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
    • C23C22/34Chemical 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 fluorides or complex fluorides

Definitions

  • the process of the invention contemplates forming a surface finishon articles of magnesium and magnesium-base alloys by subjecting the article to the action of an aqueous solution essentially comprising a water-soluble cative coatings applied thereto to provide a highly corrosion-resistant film on the metal article.
  • the treating bath according to the invention may contain any watersoiuble fluoride.
  • Hydrofiuoric acid simple fluorides such as sodium fluoride, acid fluorides such as potassium bifluoride. and complex compounds centration of 0.2 to 7 per centby weight of hydrogen chloride in the bath is desirable.
  • nitric acid the preferred range is between about 4 and about 20 per cent by weight.
  • Other acids should be used in corresponding dilutions. Concentrations of the fluoride and the acid lower than those stated are less effective in the treatment according to the invention, and concentrations higher than the preferred ranges given tend to increase the attack on the magnesium surface and to produce a much less desirable surface finish.
  • the article of magnesium or magnesium-base alloy is first freed of surface. contamination, grease, etc., by wire-brushing, sanding, or chemical cleaning. Itis then subjected to the action of an aqueous fluoride-acid solution of the type described by spraying or washing the solution on the metal, or by immersing' the article in the A solution.
  • the temperature of the treating solusuch as fluosilicic acid, fluoboric acid, and their salts, are all suitable.
  • the bath also may comprise any a'cid chemically reactive with metallic magnesium.
  • the common strong mineral acids e. g., hydrochloric, nitric, and sulfuric acids, are ordinarily employed, but other acids, both inorganic and organic, e.
  • g.,.phosphoric, acetic, chloroacetlc, and citric acids, and the like may also aqueous solutions of these materials are by far 7 the most satisfactory in the process.
  • the fluoride is preferably used in a concentration corresponding to between about 0.2 and about 6 per cent by weight of fluorine in the solution. If hydrochloric acld'ls employed as the acid, a contion' is not critical, ordinary room temperature being convenient. Immersion times of 0.5 to 2 minutes are customary, although somewhat longer times are not detrimental. After treatment the article is rinsed in water or in dilute aqueous alkali to remove the acid solution, and is then usually allowed to dry.
  • the fluoride-acid bath imparts a pleasing surface appearance and a protective coating to the article, which for many purposes may be then used without further treatment.
  • the surface finish resulting from the process is especially suited to serve as a base for additional protective coatings, such as chemical and anodie coatings, electrodeposlted metal films. and particularly siccative or resinous films, such as paints and enamels.
  • additional protective coatings such as chemical and anodie coatings, electrodeposlted metal films. and particularly siccative or resinous films, such as paints and enamels.
  • the surface treated article is given a primer coat and then several finish coats of the paint.
  • the resulting finished surface is highly corrosionresistant, much more than that of similar painted articles which have not been previously treated according to the invention, principally because of the improved adherence of the paint film.
  • Example 1 Rolled sheets of a magnesium-base alloy containing 4.0 per cent aluminum and 0.3 per cent manganese, the balance being substantially magnesium, were carefully cleaned to remove grease and dirt. They were then immersed at room temperature for one minute in a water solution,
  • Example 1 Sheets prepared as-in Examples 1 and 2, and.
  • the invention pro- Vides an unusually advantageous method of finishing and protecting the surface of articles of magnesium and. its alloys- Unlike most prior processes, only a single treatment is required; the chemicals used are inexpensive and in low concentration. No electrolytic apparatus is needed.
  • the process is extremely simple, rapid, and effective.
  • thestep which comprises subjecting the article to the action of a solution consisting of water, an acid reactive with metallic magnesium and a water soluble fluoride, the latter being employed in a concentration corresponding to between about 0.2 and about 6-per cent by weight of fluorine in the solution.
  • a process according to claim 2 ing present in a concentration of between about 0.2 and about '1 per cent by weightof hydrogen chloride in the solution.
  • the method of treating the surface of articles of magnesium and magnesium-base alloys which comprises: subjecting the article to the action of a solution consisting of water, a water soluble fluoride, and a strong mineral acid; rinsing the article to remove the treating solution; drying; and covering the dried article with a sic- HERBERT K. DE LONG.

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Chemical Treatment Of Metals (AREA)

Description

Patented July 7, 1942 UNITED STATES PATENT- OFFICE SURFACE TREATMENT or MAGNESIUM AND rrs armors Herbert K. De Long,'Midland, Micla, assignor to The Dow Chemical Company, Midland, Mich, a corporation of Michigan No Drawing.
6 Claims.
sistant.
Application April 13, 1940, Serial No. 329,533
(opus-s) Briefly, the process of the invention contemplates forming a surface finishon articles of magnesium and magnesium-base alloys by subjecting the article to the action of an aqueous solution essentially comprising a water-soluble cative coatings applied thereto to provide a highly corrosion-resistant film on the metal article.
In so far as I am aware, the treating bath according to the invention may contain any watersoiuble fluoride. Hydrofiuoric acid, simple fluorides such as sodium fluoride, acid fluorides such as potassium bifluoride. and complex compounds centration of 0.2 to 7 per centby weight of hydrogen chloride in the bath is desirable. In the case of nitric acid, the preferred range is between about 4 and about 20 per cent by weight. Other acids should be used in corresponding dilutions. Concentrations of the fluoride and the acid lower than those stated are less effective in the treatment according to the invention, and concentrations higher than the preferred ranges given tend to increase the attack on the magnesium surface and to produce a much less desirable surface finish.
In carrying the inventioninto practice, the article of magnesium or magnesium-base alloy is first freed of surface. contamination, grease, etc., by wire-brushing, sanding, or chemical cleaning. Itis then subjected to the action of an aqueous fluoride-acid solution of the type described by spraying or washing the solution on the metal, or by immersing' the article in the A solution. The temperature of the treating solusuch as fluosilicic acid, fluoboric acid, and their salts, are all suitable. The bath also may comprise any a'cid chemically reactive with metallic magnesium. The common strong mineral acids, e. g., hydrochloric, nitric, and sulfuric acids, are ordinarily employed, but other acids, both inorganic and organic, e. g.,.phosphoric, acetic, chloroacetlc, and citric acids, and the like, may also aqueous solutions of these materials are by far 7 the most satisfactory in the process. The fluoride is preferably used in a concentration corresponding to between about 0.2 and about 6 per cent by weight of fluorine in the solution. If hydrochloric acld'ls employed as the acid, a contion' is not critical, ordinary room temperature being convenient. Immersion times of 0.5 to 2 minutes are customary, although somewhat longer times are not detrimental. After treatment the article is rinsed in water or in dilute aqueous alkali to remove the acid solution, and is then usually allowed to dry.
The fluoride-acid bath imparts a pleasing surface appearance and a protective coating to the article, which for many purposes may be then used without further treatment. However, the surface finish resulting from the process is especially suited to serve as a base for additional protective coatings, such as chemical and anodie coatings, electrodeposlted metal films. and particularly siccative or resinous films, such as paints and enamels. In applying these latter'films, the surface treated article is given a primer coat and then several finish coats of the paint. The resulting finished surface is highly corrosionresistant, much more than that of similar painted articles which have not been previously treated according to the invention, principally because of the improved adherence of the paint film.
The following examples will illustrate the invention, but are not to be construed as limiting itsscope:
' Example 1 Rolled sheets of a magnesium-base alloy containing 4.0 per cent aluminum and 0.3 per cent manganese, the balance being substantially magnesium, were carefully cleaned to remove grease and dirt. They were then immersed at room temperature for one minute in a water solution,
containing 1.2 per cent by weight ofhydrogen water and dried.
fluoride (HF) and 0.68 per cent of hydrogen chloride (HOD, after which they were rinsed in Example 2 The process describedin Example 1 was re peated, except that the treating 'bath was a water solution containing 3.6 per cent by weight of hydrogen fluoride (HF) and 11.6 per cent by weight of nitric acid (HNOa) Example 3 Sheets prepared as-in Examples 1 and 2, and.
similar sheets which had been cleaned but had acid.
was bent double. The untreated sheets, in contrast, showed a much poorer corrosion resistance, and the paint fllms were far less adherent.
It will be appreciated that the invention pro- Vides an unusually advantageous method of finishing and protecting the surface of articles of magnesium and. its alloys- Unlike most prior processes, only a single treatment is required; the chemicals used are inexpensive and in low concentration. No electrolytic apparatus is needed.
The process is extremely simple, rapid, and effective.
cative coating.
2. In a method of treating the surface of articles of magnesium and magnesium-base alloys, thestep which comprises subjecting the article to the action of a solution consisting of water, an acid reactive with metallic magnesium and a water soluble fluoride, the latter being employed in a concentration corresponding to between about 0.2 and about 6-per cent by weight of fluorine in the solution.
3. A process according to claim 2 wherein the acid employed is nitric acid, the same being present in a concentration between about 4 and about 20 per cent by weight of the solution.
4. A process according to claim 2 ing present in a concentration of between about 0.2 and about '1 per cent by weightof hydrogen chloride in the solution.
5. An article formed of magnesium or a magnesium-base alloy the surface of which is covered with a protective coating prepared according to the process of claim 1.
6. The method of treating the surface of articles of magnesium and magnesium-base alloys which comprises: subjecting the article to the action of a solution consisting of water, a water soluble fluoride, and a strong mineral acid; rinsing the article to remove the treating solution; drying; and covering the dried article with a sic- HERBERT K. DE LONG.
I wherein the acid employed is hydrochloric acid, the same be-
US329533A 1940-04-13 1940-04-13 Surface treatment of magnesium and its alloys Expired - Lifetime US2288995A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US329533A US2288995A (en) 1940-04-13 1940-04-13 Surface treatment of magnesium and its alloys

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US329533A US2288995A (en) 1940-04-13 1940-04-13 Surface treatment of magnesium and its alloys

Publications (1)

Publication Number Publication Date
US2288995A true US2288995A (en) 1942-07-07

Family

ID=23285852

Family Applications (1)

Application Number Title Priority Date Filing Date
US329533A Expired - Lifetime US2288995A (en) 1940-04-13 1940-04-13 Surface treatment of magnesium and its alloys

Country Status (1)

Country Link
US (1) US2288995A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2659252A (en) * 1952-05-09 1953-11-17 Aluminum Co Of America Fabrication of light metals
US3119745A (en) * 1958-04-25 1964-01-28 Commissariat Energie Atomique Process for preventing oxidation of nuclear reactor coolant channel magnesium sheaths
US3180728A (en) * 1960-10-03 1965-04-27 Olin Mathieson Aluminum-tin composition
US3247297A (en) * 1961-03-03 1966-04-19 Commissariat Energie Atomique Process for the preparation of metallic materials by compression of a magnesium or magnesium alloy powder
US3419440A (en) * 1967-04-13 1968-12-31 Montedison Spa Solid composition for the pickling of stainless steels and alloys with a high content of chrome
US4349390A (en) * 1979-12-07 1982-09-14 Norsk Hydro A.S. Method for the electrolytical metal coating of magnesium articles
US5683522A (en) * 1995-03-30 1997-11-04 Sundstrand Corporation Process for applying a coating to a magnesium alloy product
US20070039829A1 (en) * 2005-08-17 2007-02-22 Trevor Pearson Pretreatment of magnesium substrates for electroplating
US20080248325A1 (en) * 2006-11-16 2008-10-09 Yamaha Hatsudoki Kabushiki Kaisha Magnesium alloy part and production method thereof

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2659252A (en) * 1952-05-09 1953-11-17 Aluminum Co Of America Fabrication of light metals
US3119745A (en) * 1958-04-25 1964-01-28 Commissariat Energie Atomique Process for preventing oxidation of nuclear reactor coolant channel magnesium sheaths
US3180728A (en) * 1960-10-03 1965-04-27 Olin Mathieson Aluminum-tin composition
US3247297A (en) * 1961-03-03 1966-04-19 Commissariat Energie Atomique Process for the preparation of metallic materials by compression of a magnesium or magnesium alloy powder
US3419440A (en) * 1967-04-13 1968-12-31 Montedison Spa Solid composition for the pickling of stainless steels and alloys with a high content of chrome
US4349390A (en) * 1979-12-07 1982-09-14 Norsk Hydro A.S. Method for the electrolytical metal coating of magnesium articles
US5683522A (en) * 1995-03-30 1997-11-04 Sundstrand Corporation Process for applying a coating to a magnesium alloy product
US20070039829A1 (en) * 2005-08-17 2007-02-22 Trevor Pearson Pretreatment of magnesium substrates for electroplating
US7704366B2 (en) 2005-08-17 2010-04-27 Trevor Pearson Pretreatment of magnesium substrates for electroplating
US20080248325A1 (en) * 2006-11-16 2008-10-09 Yamaha Hatsudoki Kabushiki Kaisha Magnesium alloy part and production method thereof
EP1932946A3 (en) * 2006-11-16 2010-09-22 Yamaha Hatsudoki Kabushiki Kaisha Magnesium alloy part and production method thereof
US7935427B2 (en) 2006-11-16 2011-05-03 Yamaha Hatsudoki Kabushiki Kaisha Magnesium alloy part and production method thereof

Similar Documents

Publication Publication Date Title
US2851385A (en) Process and composition for coating aluminum surfaces
JPH09501469A (en) Compositions and methods for treating phosphated metal surfaces
US2288995A (en) Surface treatment of magnesium and its alloys
US2789070A (en) Composition and process for phosphatizing metal
US3539403A (en) Solutions for the deposition of protective layers on zinc surfaces and process therefor
US2213263A (en) Process of coating metals
JP5733671B2 (en) Pretreatment process for aluminum and high etch cleaner used therein
US4451304A (en) Method of improving the corrosion resistance of chemical conversion coated aluminum
US1947122A (en) Surface treatment of magnesium and magnesium base alloys
US3081238A (en) Electrolytic treatment of metal surfaces
US2927046A (en) Coated metals and solutions and process for making the same
US2835616A (en) Procedure for the manufacture of oxalate coatings on metals
US2511988A (en) Pickling process
US4617068A (en) Composition and process for treatment of ferrous substrates
US2719796A (en) Process for enameling aluminum
JP3083873B2 (en) Post-cleaning method of chemical conversion coating and use of this method
US3615892A (en) Composition and method for black coating on metals
US2760890A (en) Composition for and method of producing corrosion resistant metal coating
US2827402A (en) Method of pickling titanium and titanium alloys
US4316752A (en) Oxalic acid treatment of carbon steel, galvanized steel and aluminum surfaces
JPS6256579A (en) Acidic aqueous solution and method for passivating surface of zinc or zinc/aluminum alloy
US2795518A (en) Process for treating steel, zinc, and aluminum to increase corrosion resistance
US2628925A (en) Bright corrosion resistant coating of metals
US2791525A (en) Composition for and method of forming oxalate coatings on ferrous metal surfaces
US2245609A (en) Metal finishing process