US1953999A - Anodic coating of zinc base metals - Google Patents

Anodic coating of zinc base metals Download PDF

Info

Publication number
US1953999A
US1953999A US642610A US64261032A US1953999A US 1953999 A US1953999 A US 1953999A US 642610 A US642610 A US 642610A US 64261032 A US64261032 A US 64261032A US 1953999 A US1953999 A US 1953999A
Authority
US
United States
Prior art keywords
zinc
coating
anodic
metal
anode
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
US642610A
Inventor
Truesdale Edward Cushman
Wilhelm Ernest John
Reinhard Claude Edward
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.)
New Jersey Zinc Co
Original Assignee
New Jersey Zinc 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 New Jersey Zinc Co filed Critical New Jersey Zinc Co
Priority to US642610A priority Critical patent/US1953999A/en
Priority claimed from GB133234A external-priority patent/GB421696A/en
Application granted granted Critical
Publication of US1953999A publication Critical patent/US1953999A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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

Definitions

  • This invention relates to, the coating of zinc base metals by anodic action, and has for its object the provision of an improved method of producing useful anodic coatings on such metals, as well as the provision, as new articles of commerce, of zinc base metals so coated.
  • zinc base meta1 we mean metals and alloys composed principally of zinc.
  • the invention is particularly concerned with the production bf anodic coatings on zinc and zinc base alloys for the purpose of protection, ornamentation, or of serving as a base for the application of paints, lacquers and the like so as to secure good adhesion of the latter.
  • Ordinary commercial zinc (inparticular, rolled or strip zinc), zinc base alloys such as die-casting alloys containing over 90% zinc for example, the alloys of 'United States Patents Nos, 1,596,761, 1,663,215, 1,779,525, 1,852,434, 1,852,441 and 1,852,- 442)
  • wrought zinc base alloys for example, the alloys of United States Patents Nos.
  • 1,716,599, 1,832,653, 1,832,733 and 1,835,450 may be advantageously coated by the method of the invention.
  • Numerous other zinc base alloys, particularly those containing small amounts of copper and/or aluminum, are likewise amenable to treatment in accordance with the invention.
  • anodic coatings can be produced on zinc with substantially neutral electrolytes containing an anion (other thanhydrox'yl ion) capable of producing by anodic action with zinc an insoluble coating on the zinc anode, or containing an anion (other than hydroxyl ion) capable of forming an insoluble compound with zinc.
  • Such coatings vary in color depending upon the nature of the dominant anion, and while the coating may contain some zinc oxide, it is characterized by a substantial content of the dominant anion or a derivative thereof.
  • the method of thepresent invention involves subjecting a zinc base metal, as anode, to electrolytic treat-
  • the articles of zinc or zinc base alloys to be coated are subjected to an electrolytic treatment as anode while immersed in a substantially'neutral electrolyte con taining an anion of the characteristic properties hereinbefore described.
  • the zinc articles become coated. with a firm adherent film which contains a ysubstantialfl amount of the dominant anion or a derivative thereof.
  • the coating may consist of insoluble compounds (usually insoluble compounds of zinc) formed by anodic reaction of zinc with an'ions other than hydroxyl ions present in the electrolyte, or of combinations of such or other insoluble compounds with zinc oxide.
  • insoluble compounds usually insoluble compounds of zinc
  • an'ions other than hydroxyl ions present in the electrolyte or of combinations of such or other insoluble compounds with zinc oxide.
  • the composition of the coating produced in any particular electrolyte will depend upon the relative amounts of hydroxyl ions and other anions (capable of' forming an insoluble compound with zinc or by anodic action with azinc anode) which are discharged at the zinc anode, and in turn, the relative concentrations and relative reactivities of hydroxyl and other anions will determine which of these will be predominantly discharged at the anode.
  • the appearance of the coating may be improved by bufllng the zinc article before anodic treatment.
  • the cathode used in the anodic treatment may be of nickel, iron or other metal insoluble in the electrolyte.
  • Substantially neutral electrolytes for the pracv tice of the invention may be made up of various substances.
  • salts composed of a weak acid and a weak base, which, although highly hydrolyzed, remain essentially neutral, may be used.
  • the acid radical of such a salt should be capable of forming an insoluble'salt with zinc.
  • Ammonium hydroxide may be taken as an example of such a weak base, while carbonic acid (the zinc salt of which is insoluble) is an example of such a weak acid.
  • Salts composed of a strong base and an acid sufficiently strong to give an essentially neutral solution may also be used, as, for example, potassium ferrocyanide.
  • Substantially neutral solutions of certain oxidizing agents, and various other compounds, may likewise be used in practicing the invention, such, for example, as solutions of potassium permanganate, potassium diohromate, ammonium oxalate, ammonium-molybdate, potassium ferrocyanide, potassium ferricyanide etc. Buffers may be added to these solutions to aid in maintaining suitable pH values during operation.
  • a satisfactory neutral electrolyte for the practice of the invention is an aqueous solution of ammonium oxalate containing 35 grams of (NH4) 2C204'H2O per liter of water.
  • Anodic treatment of zinc in this electrolyte at room temperature yields an adherent coating varyingv in colorfrom white to light gray.
  • An initial current density of 24 amperes per square foot falls off to about 9.6 amperes per square foot in ten minutes of anodic treatment.
  • a hard, adherent anodic deposit ranging in color from brown to black is obtained by treating zinc or zinc base alloys in aqueous solutions of potassium permanganate.
  • concentration of potassium permanganate may vary from dilute solutions, say 10 to 20 grams per liter of water, up to a saturated solution.
  • the preferred operating conditions are a temperature of room temperatures to 50 C., a current density of 5 to 24 amperesper square foot and a duration of treatment of from 5 to 20 minutes.
  • the use of too high a current density causes the coating to check and crack, a tendency that is decreased by operating at the higher temperature of 50 C.
  • the anodic deposit can be dyed in aqueous solutions of nigrosine or the alizarine dyes.
  • a chemical analysis of the coating (carefully removed by scraping so as not to remove any zinc from the specimen) showed the presence of about 23% of zinc and 19% of manganese, calculated as the metals.
  • the manganese compound then present was identified as MnaO4 by its X-ray pattern.
  • alkali metals such as sodium. may be substituted for potassium in the compounds hereinbefore mentioned as suitable for the practice of the invention.
  • substantially neutral solutions of alkali metal oxalates may be used in place of ammonium oxalate.
  • the anodic coatings of the invention notonly protect the zinc or zinc base alloy from corrosion but are also useful for decoration. These coatings may also be used as a base to increase the adherence of paint, enamel, lacquer, etc.
  • these coatings may be given various light or dark colors by dyeing. The color of the darker coatings may also be improved in some cases by dyeing.
  • the dyeing may take place during the electrolytic treatment by solution of the dye in the electrolyte, or dyeing may be carried out by immersion of the coated article in an appropriate solution of the dye.
  • a zinc base .metal having a thin, dense and firmly adherent anodic coating containing an insoluble compound other than or in addition to zinc oxide.
  • a zinc base metal having a thin, dense and firmly adherent anodic coating containing zinc or an insoluble compound thereof in combination with an insoluble compound derived from an anodic radical other than hydroxyl.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an anion (other than hydroxyl) capable of producing by anodic action with zinc an insoluble, adherent coating on the zinc metal.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytictreatment in a substantially neutral electrolyte containing an anion of about 6 to 8.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a solution of ammonium oxalate having a pH of about 6 to 8.
  • the method of producing 9. coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in an electrolyte containing about 35 grams of ammonium oxalate per liter.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytictreatment in an electrolyte containing potassium permanganate in amount of from about 10 grams per liter to saturation.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to' electrolytic treatment in an electrolyte containing 10 grams or more of potassium permanganate per liter, at a temperature of room-temperature to 50 C. and a current density of 5 to 24 amperes per square foot of anode surface.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing one or more substances of the group comprising potassium ferrocyanidc, potassium ferricyanide, potassium permanganate, potassium dichromate, ammonium oxalate, and ammonium molybdate.
  • the method of producing a coating; on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in an electrolyte having a pH of about 6 to 8 and concomprising potassium ferrocyanide, potassium ferricyanide, potassium permanganate, potassium dichromate, ammonium oxalate, and ammonium molybdate, and thereby producing on said zinc base metal a thin, dense and firmly adherent anodic coating containing a derivative of the anion radical of one of said substances.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an oxalate ion capable of producing by anodic action with zinc an adherent coating on the zinc metal.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an alkali metal permanganate.
  • the method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an alkali metal ferrocyanide.
  • Amethod of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte formed from a salt composed of a. weak acid and a weak base, the acid radical ,of said salt forming by anodic action an insoluble salt with the zinc adhering as a coating on the zinc base metal.
  • a method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment ina substantially neutral electrolyte formed from a salt composed of a strong base and an acid sufiiciently strong to give an essentially neutral solution, the acid radical of said salt forming by anodic action an insolublesalt with the zinc adhering as a. coating on the zinc base metal.
  • EDWARD CUSHMAN TRUE-SDALE ERNEST JOHN WILHELM. CLAUDE EDWARD REINHARD.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electroplating And Plating Baths Therefor (AREA)

Description

Patented Apr. 10, 1934 ANODIC COATING 01f ZINC BASE METALS Edward Cushman Truesdale, Ernest John Wilhelm, and Claude Edward Reinhard, Palmerton, Pa., assignors to The New Jersey Zinc Company, New York, N. Y., a corporation of New Jersey No- Drawing. Application November 14, 1932,
Serial No. 642,610
' 20 Claims. (01. 204-4) This invention relates to, the coating of zinc base metals by anodic action, and has for its object the provision of an improved method of producing useful anodic coatings on such metals, as well as the provision, as new articles of commerce, of zinc base metals so coated. By zinc base meta1 we mean metals and alloys composed principally of zinc.
The invention is particularly concerned with the production bf anodic coatings on zinc and zinc base alloys for the purpose of protection, ornamentation, or of serving as a base for the application of paints, lacquers and the like so as to secure good adhesion of the latter. Ordinary commercial zinc (inparticular, rolled or strip zinc), zinc base alloys such as die-casting alloys containing over 90% zinc (for example, the alloys of 'United States Patents Nos, 1,596,761, 1,663,215, 1,779,525, 1,852,434, 1,852,441 and 1,852,- 442), and wrought zinc base alloys (for example, the alloys of United States Patents Nos. 1,716,599, 1,832,653, 1,832,733 and 1,835,450) may be advantageously coated by the method of the invention. Numerous other zinc base alloys, particularly those containing small amounts of copper and/or aluminum, are likewise amenable to treatment in accordance with the invention.
In copending applications for Letters Patent of the United States, Serial Nos. 642,608, and 642,609 filed November 14, 1932, on behalf of two of us (Tru'esdale and Wilhelm) there is disclosed the production of useful anodic coatings on zinc f1 nn alkaline electrolytes. These coatings consist essentially of zinc oxide, are dark in color with relatively strong alkaline electrolytes and light gray to white in color withmore dilute alkaline electrolytes. In the course of an exhaustive investigation of the anodic-coating of zinc, we have discovered that useful coatings can be produced withcertain substantially neutral electrolytes..
Thus, we have found that useful anodic coatings can be produced on zinc with substantially neutral electrolytes containing an anion (other thanhydrox'yl ion) capable of producing by anodic action with zinc an insoluble coating on the zinc anode, or containing an anion (other than hydroxyl ion) capable of forming an insoluble compound with zinc. Such coatings vary in color depending upon the nature of the dominant anion, and while the coating may contain some zinc oxide, it is characterized by a substantial content of the dominant anion or a derivative thereof.
The method of thepresent invention, based on the foregoing discoveries, involves subjecting a zinc base metal, as anode, to electrolytic treat- In carrying out the invention, the articles of zinc or zinc base alloys to be coated are subjected to an electrolytic treatment as anode while immersed in a substantially'neutral electrolyte con taining an anion of the characteristic properties hereinbefore described. When so treated at appropriate voltages, current densities and temperatures, the zinc articles become coated. with a firm adherent film which contains a ysubstantialfl amount of the dominant anion or a derivative thereof. Thus, the coating may consist of insoluble compounds (usually insoluble compounds of zinc) formed by anodic reaction of zinc with an'ions other than hydroxyl ions present in the electrolyte, or of combinations of such or other insoluble compounds with zinc oxide. In general, the composition of the coating produced in any particular electrolyte will depend upon the relative amounts of hydroxyl ions and other anions (capable of' forming an insoluble compound with zinc or by anodic action with azinc anode) which are discharged at the zinc anode, and in turn, the relative concentrations and relative reactivities of hydroxyl and other anions will determine which of these will be predominantly discharged at the anode.
Since the anodic coating of the invention usually rep'roducea'in-rhihute detail, the surface markings originally present on the zinc article, the appearance of the coating may be improved by bufllng the zinc article before anodic treatment.v
. remove the residual cleaning solution, following which the zinc article is ready for anodic treatment.
The cathode used in the anodic treatment may be of nickel, iron or other metal insoluble in the electrolyte.
Substantially neutral electrolytes for the pracv tice of the invention may be made up of various substances. Thus, salts composed of a weak acid and a weak base, which, although highly hydrolyzed, remain essentially neutral, may be used.
The acid radical of such a salt should be capable of forming an insoluble'salt with zinc. Ammonium hydroxide may be taken as an example of such a weak base, while carbonic acid (the zinc salt of which is insoluble) is an example of such a weak acid. Salts composed of a strong base and an acid sufficiently strong to give an essentially neutral solution may also be used, as, for example, potassium ferrocyanide. Substantially neutral solutions of certain oxidizing agents, and various other compounds, may likewise be used in practicing the invention, such, for example, as solutions of potassium permanganate, potassium diohromate, ammonium oxalate, ammonium-molybdate, potassium ferrocyanide, potassium ferricyanide etc. Buffers may be added to these solutions to aid in maintaining suitable pH values during operation.
A satisfactory neutral electrolyte for the practice of the invention is an aqueous solution of ammonium oxalate containing 35 grams of (NH4) 2C204'H2O per liter of water. Anodic treatment of zinc in this electrolyte at room temperature yields an adherent coating varyingv in colorfrom white to light gray. An initial current density of 24 amperes per square foot falls off to about 9.6 amperes per square foot in ten minutes of anodic treatment. Initial current densities of from 14 to 72 amperes per square foot have been used, and the operating temperature and composition of the electrolyte may likewise be varied, but the stated conditions are satisfact ry.- Such anodic coatings may be dyed with a izarine or with nigrosine dyes. Analysis of an anodic coating produced under the specified conditions showed it to contain about 73% of zinc oxalate.
Anodic treatment of zinc and zinc base alloys in a solution containing 50 grams of potassium ferrocyanide (K4Fe(CN) 6'3H20) per liter of water, for three minutes at. an initial current density of 24 amperesper square foot at room temperature, produces a thin, adherent, iridescent coating, ranging in color from pink to green. On account of polarization, the current density drops rapidly. Thus, in the example given,- the current density may drop from the initial value of 24 amperes to less than'0.5 amperes per square foot in less than one minute. Because of this fact, the solution may be operated within a rather wide range of initial current densities, while the time of treatment may be more or less than three minutes.
The operating temperature of the solution, and
its composition may also be varied, but the conditions specified are preferred.
A hard, adherent anodic deposit ranging in color from brown to black is obtained by treating zinc or zinc base alloys in aqueous solutions of potassium permanganate. The concentration of potassium permanganate may vary from dilute solutions, say 10 to 20 grams per liter of water, up to a saturated solution. The preferred operating conditions are a temperature of room temperatures to 50 C., a current density of 5 to 24 amperesper square foot and a duration of treatment of from 5 to 20 minutes. The use of too high a current density causes the coating to check and crack, a tendency that is decreased by operating at the higher temperature of 50 C. These conditions may be varied without departing from the spirit of the invention. The anodic deposit can be dyed in aqueous solutions of nigrosine or the alizarine dyes. A chemical analysis of the coating (carefully removed by scraping so as not to remove any zinc from the specimen) showed the presence of about 23% of zinc and 19% of manganese, calculated as the metals. Upon heating the coating to a temperature between 700 and 800 C., the manganese compound then present was identified as MnaO4 by its X-ray pattern.
Other alkali metals, such as sodium. may be substituted for potassium in the compounds hereinbefore mentioned as suitable for the practice of the invention. Similarly substantially neutral solutions of alkali metal oxalates may be used in place of ammonium oxalate.
The anodic coatings of the invention notonly protect the zinc or zinc base alloy from corrosion but are also useful for decoration. These coatings may also be used as a base to increase the adherence of paint, enamel, lacquer, etc. When the coatings produced in accordance with the invention are light in color, these coatings may be given various light or dark colors by dyeing. The color of the darker coatings may also be improved in some cases by dyeing. The dyeing may take place during the electrolytic treatment by solution of the dye in the electrolyte, or dyeing may be carried out by immersion of the coated article in an appropriate solution of the dye.
We claim:
1. As a new article of commerce, a zinc base .metal having a thin, dense and firmly adherent anodic coating containing an insoluble compound other than or in addition to zinc oxide.
2. As a new article of commerce, a zinc base metal having a thin, dense and firmly adherent anodic coating containing zinc oxide in combina-v tion with another insoluble compound.
3. As a new article of commerce, a zinc base metal having a thin, dense and firmly adherent anodic coating containing zinc or an insoluble compound thereof in combination with an insoluble compound derived from an anodic radical other than hydroxyl.
4. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an anion (other than hydroxyl) capable of producing by anodic action with zinc an insoluble, adherent coating on the zinc metal.
5. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytictreatment in a substantially neutral electrolyte containing an anion of about 6 to 8.
(other than hydroxyl) capable of forming an insoluble compound withzinc. i 6. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a solution of ammonium oxalate having a pH of about 6 to 8.
7. The method of producing 9. coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in an electrolyte containing about 35 grams of ammonium oxalate per liter.
1 8. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a solution of potassium ierrocyanide having a pH 9. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in an electrolyte containing about 50 grams of potassium ferrocyanide per liter.
10. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a solution of potassium permanganate having a pH of about 6 to 8. r
11. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytictreatment in an electrolyte containing potassium permanganate in amount of from about 10 grams per liter to saturation.
12. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to' electrolytic treatment in an electrolyte containing 10 grams or more of potassium permanganate per liter, at a temperature of room-temperature to 50 C. and a current density of 5 to 24 amperes per square foot of anode surface.
13. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing one or more substances of the group comprising potassium ferrocyanidc, potassium ferricyanide, potassium permanganate, potassium dichromate, ammonium oxalate, and ammonium molybdate.
14. The method of producing a coating; on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in an electrolyte having a pH of about 6 to 8 and concomprising potassium ferrocyanide, potassium ferricyanide, potassium permanganate, potassium dichromate, ammonium oxalate, and ammonium molybdate, and thereby producing on said zinc base metal a thin, dense and firmly adherent anodic coating containing a derivative of the anion radical of one of said substances.
15-. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an oxalate ion capable of producing by anodic action with zinc an adherent coating on the zinc metal.
16. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an alkali metal permanganate.
17. The method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte containing an alkali metal ferrocyanide.
18. Amethod of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment in a substantially neutral electrolyte formed from a salt composed of a. weak acid and a weak base, the acid radical ,of said salt forming by anodic action an insoluble salt with the zinc adhering as a coating on the zinc base metal.
19. A method of producing a coating on a zinc base metal which comprises subjecting the metal as anode to electrolytic treatment ina substantially neutral electrolyte formed from a salt composed of a strong base and an acid sufiiciently strong to give an essentially neutral solution, the acid radical of said salt forming by anodic action an insolublesalt with the zinc adhering as a. coating on the zinc base metal.
being adapted to produce by anodic action with the zinc an insoluble adherent coating on the zinc base metal.
EDWARD CUSHMAN TRUE-SDALE. ERNEST JOHN WILHELM. CLAUDE EDWARD REINHARD.
US642610A 1932-11-14 1932-11-14 Anodic coating of zinc base metals Expired - Lifetime US1953999A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US642610A US1953999A (en) 1932-11-14 1932-11-14 Anodic coating of zinc base metals

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US642610A US1953999A (en) 1932-11-14 1932-11-14 Anodic coating of zinc base metals
GB133234A GB421696A (en) 1934-01-13 1934-01-13 Anodic coating of zinc base metals

Publications (1)

Publication Number Publication Date
US1953999A true US1953999A (en) 1934-04-10

Family

ID=26236658

Family Applications (1)

Application Number Title Priority Date Filing Date
US642610A Expired - Lifetime US1953999A (en) 1932-11-14 1932-11-14 Anodic coating of zinc base metals

Country Status (1)

Country Link
US (1) US1953999A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2469015A (en) * 1943-02-20 1949-05-03 United Chromium Inc Method and compositions for producing surface conversion coatings on zinc

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2469015A (en) * 1943-02-20 1949-05-03 United Chromium Inc Method and compositions for producing surface conversion coatings on zinc

Similar Documents

Publication Publication Date Title
US4744872A (en) Anodizing solution for anodic oxidation of magnesium or its alloys
US2231373A (en) Coating of articles of aluminum or aluminum alloys
US4082626A (en) Process for forming a silicate coating on metal
US3098018A (en) Sealing anodized aluminum
US3066055A (en) Process and composition for producing aluminum surface conversion coatings
US2096309A (en) Surface treatment of aluminum and aluminum alloys
DE102011002837A1 (en) Multi-stage pre-treatment of tinplate before painting
US2949411A (en) Titanium anodizing process
US3454483A (en) Electrodeposition process with pretreatment in zinc phosphate solution containing fluoride
US1965269A (en) Method of coloring aluminum
CA1134774A (en) Anodising aluminium
GB1590597A (en) Treating a1 or a1 alloy surfaces
US3011958A (en) Anodic treatment of zinc and zinc-base alloys
US1953999A (en) Anodic coating of zinc base metals
US2339806A (en) Surface treatment of aluminum and aluminum alloys
US2206028A (en) Anodic treatment of magnesium
US3518169A (en) Alkali solution treatment of cathodically chromated metal surface
US1953998A (en) Anodic coating of zinc base metals
US2322205A (en) Method of treating magnesium and its alloys
US2431728A (en) Treatment of ferrous metals to improve resistance to rusting
US5120405A (en) Method of coloring aluminum or aluminum alloy material
US2095519A (en) Method for producing galvanic coatings on aluminum or aluminum alloys
US3620939A (en) Coating for magnesium and its alloys and method of applying
US3531384A (en) Process of treating surfaces of metallic articles
US3787298A (en) Anodizing aluminum foams