US20060042726A1 - Non-chrome passivation of steel - Google Patents

Non-chrome passivation of steel Download PDF

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Publication number
US20060042726A1
US20060042726A1 US10/933,014 US93301404A US2006042726A1 US 20060042726 A1 US20060042726 A1 US 20060042726A1 US 93301404 A US93301404 A US 93301404A US 2006042726 A1 US2006042726 A1 US 2006042726A1
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United States
Prior art keywords
recited
composition
metal
fluoacid
polyoxyethylene
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Abandoned
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US10/933,014
Inventor
Andrea Keys
Jeffrey Melzer
Michael Raab
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Chemetall Corp
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General Electric Co
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Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Priority to US10/933,014 priority Critical patent/US20060042726A1/en
Assigned to GENERAL ELECTRIC COMPANY reassignment GENERAL ELECTRIC COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KEYS, ANDREA, MELZER, JEFFREY I., RAAB, MICHAEL T.
Priority to BRPI0515626A priority patent/BRPI0515626B1/en
Priority to PCT/US2005/031091 priority patent/WO2006028894A2/en
Priority to CN2005800294625A priority patent/CN101018888B/en
Priority to CA2578965A priority patent/CA2578965C/en
Priority to ES05793978.7T priority patent/ES2573537T3/en
Priority to EP05793978.7A priority patent/EP1838898B1/en
Priority to RU2007111918/02A priority patent/RU2396370C2/en
Priority to AU2005282751A priority patent/AU2005282751B2/en
Priority to MX2007002619A priority patent/MX2007002619A/en
Publication of US20060042726A1 publication Critical patent/US20060042726A1/en
Assigned to CHEMETALL CORP. reassignment CHEMETALL CORP. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GE BETZ INTERNATIONAL, INC., GE BETZ, INC., GENERAL ELECTRIC COMPANY
Priority to US12/154,502 priority patent/US8980015B2/en
Abandoned legal-status Critical Current

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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
    • C23C22/36Chemical 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 containing also phosphates
    • C23C22/361Chemical 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 containing also phosphates containing titanium, zirconium or hafnium compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D119/00Coating compositions based on rubbers, not provided for in groups C09D107/00 - C09D117/00
    • C09D119/02Latex
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D121/00Coating compositions based on unspecified rubbers
    • C09D121/02Latex
    • 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
    • C23C22/82After-treatment
    • C23C22/83Chemical after-treatment

Definitions

  • the present invention relates to non-chromate coatings for metals. More particularly, the present invention relates to non-chromate coatings for steel surfaces to improve corrosion resistance and adhesion of paints to the surface.
  • the invention provides a dried in place coating which is particularly effective at treating galvanized steel coil strip.
  • a chromate conversion coating on the surface of galvanized steel are to provide corrosion resistance, improve adhesion of coatings and for aesthetic reasons. Chromate passivation of a galvanized steel surface is done to provide corrosion resistance and for aesthetic reasons on materials which are not to be painted.
  • the conversion coating improves adhesion of coating layers such as paints, inks, lacquers and plastic coatings.
  • Galvanized steel is typically treated with an aqueous composition containing hexavalent or trivalent chromium ions with other additives to create a chromium conversion coating.
  • the present invention provides a method of treating the surface of metals, such as steel or galvanized steel, to provide for the formation of a coating which increases the corrosion resistance and adhesion properties of the metal surface.
  • the passivation or conversion coating formed by the present invention may be dried in place or rinsed.
  • the methods of the invention comprise contacting the requisite metal surface with a chromate free aqueous treatment composition comprising: (a) a film forming latex polymer; (b) a fluoacid; (c) phosphoric acid; and (d) a polyoxyethylene/oxypropylene block copolymer.
  • an improved, non-chromate conversion or passivation coating can be provided on metal surfaces, particularly galvanized steel surfaces, by contacting the surface with an aqueous coating solution or dispersion of:
  • compositions of the invention have been found to provide an aqueous pretreatment agent for the treatment of galvanized metal surfaces which provides improved corrosion resistance and adhesion of latex applied coating when the treatment is dried in place.
  • the film forming latex polymer component this can be chosen from a wide variety of materials such as styrene-butadiene copolymers, acrylate resins, polyvinylacetate, urethanes, amido-amine polymers, and similar materials.
  • Some commercially available latex materials include: Description Type “Neocar” (Union Carbide) Vinyl Ester/Acrylic “Res 3077” (Rohm & Haas) Vinyl Acetate/Acrylic “Airflex” 500 (Air Products) Vinyl Acetate/Ethylene “Airflex 4514 (Air Products) Vinyl Chloride/Amide Terpolymer Airflex 4500 (Air Products) Vinyl Chloride/Amide Terpolymer Flexhane 620 (Air Products) Urethane Vinac 884 (Air Products) Vinyl Acetate Dow 620 (Dow) SBR Airflex 4530 (Air Products) ethylene vinyl chloride Kymene 736 polyamido amine U Car Latex 651 acrylate
  • U Car Latex 651 As the film forming latex polymer component. This is commercially available form Union Carbide and is reportedly an acrylic copolymer resin emulsion having as major latex components butyl acrylate, methyl methacrylate, and methacrylic acid polymers.
  • this is preferably a fluoacid of a Group IVB metal or mixtures thereof.
  • Fluotitanic acid H 2 TiF 6 is presently preferred with fluozirconic acid, H 2 ZrF 6 , also mentioned as exemplary. Combinations of these acids are also used.
  • phosphoric acid As stated above, phosphoric acid, H 3 PO 4 , and salts thereof are also present in the treatment formulation.
  • phosphoric acid refers to both the acid and salt form.
  • a polyoxyethylene/oxypropylene block copolymer is exemplary.
  • the ethylene oxide (EO):propylene oxide (PO) repeat units of the copolymers may be present in a molar ratio of about 1:1-9; preferably 1:5-9; most preferably 1:9. Molecular weights of these block copolymers will range from about 2,000-4,000.
  • These copolymers are commercially available from BASF under the “Pluronic” trademark. Presently, “Pluronic 101” is preferred for use.
  • This specific copolymer has a ratio of EO:PO blocks of about 1:9 and a molecular weight of about 3,300.
  • compositions in accordance with the invention are chromate free and include 0.01-50 wt % film forming latex 0.01-40 wt % H 3 PO 4 0.01-30 wt % fluoacid 0.01-20 wt % non-ionic polymer surfactant wherein the weight of the composition is, in total, 100 wt %.
  • compositions having the following range (in wt %) of the components 1-20 wt % film forming latex 1-50 wt % H 3 PO 4 1-40 wt % fluoacid 0.01-15 wt % non-ionic polymer surfactant remainder water.
  • the sum of all composition components equals 100 wt %.
  • the pH of the compositions may vary from about 1.0 to 2.0.
  • the requisite metal surface may be contacted by the treatment in spray, immersion or roller applications.
  • the treatment is then dried and the metal surface is ready for painting or other coating applications.
  • the conversion or passivation treatment of the present invention is applied to result in a conversion coating weight of greater than about 1 milligram per square foot to treated surface with a weight of 2-150 milligrams per square foot being more preferred.
  • working solutions comprising about 3-100, preferably 10-100 wt % concentrations of the above “More preferred” formulation are used to contact the desired metal surfaces.
  • One tested treatment candidate formulation “A” was a latex emulsion including the following components: 1) U Car Latex 651 5.8 wt % (65% actives) 2) H 3 PO 4 22.0 wt % 3) Fluotitanic acid 10 wt % 4) Pluronic 101 0.5 wt % 5) Water remainder
  • U Car Latex 651 is an acrylic copolymer resin emulsion having a viscosity 20° C., cP (Brookfield, LVT #3, 50 rpm) of 400 and a particle size in microns of 0.45. It is available from the Union Carbide Corporation of Danbury, Conn. Its major constituents are 1) butyl acrylate, methyl methacrylate, methacrylic acid polymers in an amount of ⁇ 65 wt %; 2) water ⁇ 35%; 3) glycols, polyethylene, mono [(1,1,3,3-tetramethylbutyl)phenyl] ether in an amount of less than 2%; and 4) ammonia in 0.2 wt %. It is a white liquid.
  • cP Brookfield, LVT #3, 50 rpm
  • Pluronic 101 is a difunctional block copolymer surfactant terminating in primary hydroxy groups and is available from BASF Corporation in Mount Olive, N.J. It is a block copolymer having hydrophobic propylene oxide (PO) repeat units and hydrophilic ethylene oxide (EtO) repeat units in a molar ratio of about 9:1. The overall molecular weight of the copolymer is about 3300.
  • PO propylene oxide
  • EtO hydrophilic ethylene oxide
  • Test panels for the examples were prepared as follows: G70/70 hot dipped galvanized steel test panels purchased from ACT Laboratories were spray cleaned with a 3% aqueous solution of an alkaline surfactant product and then rinsed with DI water and subsequently coated with the test treatment formulations by spin coat application, followed by forced air drying.

Abstract

Chromate free treatments and compositions for applying a conversion or passivation coating to metal surfaces. Preferred compositions comprise a film forming latex polymer, fluoacid, phosphoric acid, and a polyoxyethylene/oxypropylene block copolymer. The requisite metal surfaces are contacted by the compositions and dried. Rinsing is optional.

Description

    FIELD OF INVENTION
  • The present invention relates to non-chromate coatings for metals. More particularly, the present invention relates to non-chromate coatings for steel surfaces to improve corrosion resistance and adhesion of paints to the surface. The invention provides a dried in place coating which is particularly effective at treating galvanized steel coil strip.
  • BACKGROUND
  • The purposes of the formation of a chromate conversion coating on the surface of galvanized steel are to provide corrosion resistance, improve adhesion of coatings and for aesthetic reasons. Chromate passivation of a galvanized steel surface is done to provide corrosion resistance and for aesthetic reasons on materials which are not to be painted. The conversion coating improves adhesion of coating layers such as paints, inks, lacquers and plastic coatings. Galvanized steel is typically treated with an aqueous composition containing hexavalent or trivalent chromium ions with other additives to create a chromium conversion coating.
  • Growing concerns exist regarding the pollution effects of chromates discharged into rivers and waterways by such processes. Because of the high solubility and the strongly oxidizing character of hexavalent chromium ions, conventional chromate conversion processes require extensive waste treatment procedures to control their discharge. In addition, the disposal of the solid sludge from such waste treatment procedures is a significant problem.
  • Accordingly, there is a need in the art to provide an effective non-chromate treatment to provide a dried in place conversion or passivation coating to inhibit metal surface corrosion and enhance adhesion of paint or other coatings that may be applied to the metal surface.
  • SUMMARY OF THE INVENTION
  • The present invention provides a method of treating the surface of metals, such as steel or galvanized steel, to provide for the formation of a coating which increases the corrosion resistance and adhesion properties of the metal surface. The passivation or conversion coating formed by the present invention may be dried in place or rinsed. The methods of the invention comprise contacting the requisite metal surface with a chromate free aqueous treatment composition comprising: (a) a film forming latex polymer; (b) a fluoacid; (c) phosphoric acid; and (d) a polyoxyethylene/oxypropylene block copolymer. Other objects and advantages of the invention will be apparent from the following description and the appended claims.
  • DETAILED DESCRIPTION
  • The inventors have found that an improved, non-chromate conversion or passivation coating can be provided on metal surfaces, particularly galvanized steel surfaces, by contacting the surface with an aqueous coating solution or dispersion of:
      • (a) a film forming latex polymer;
      • (b) a fluoacid;
      • (c) phosphoric acid; and
      • (d) a nonionic polymer surfactant.
  • Compositions of the invention have been found to provide an aqueous pretreatment agent for the treatment of galvanized metal surfaces which provides improved corrosion resistance and adhesion of latex applied coating when the treatment is dried in place.
  • As to the film forming latex polymer component, this can be chosen from a wide variety of materials such as styrene-butadiene copolymers, acrylate resins, polyvinylacetate, urethanes, amido-amine polymers, and similar materials. Some commercially available latex materials include:
    Description Type
    “Neocar” (Union Carbide) Vinyl Ester/Acrylic
    “Res 3077” (Rohm & Haas) Vinyl Acetate/Acrylic
    “Airflex” 500 (Air Products) Vinyl Acetate/Ethylene
    “Airflex 4514 (Air Products) Vinyl Chloride/Amide Terpolymer
    Airflex 4500 (Air Products) Vinyl Chloride/Amide Terpolymer
    Flexhane 620 (Air Products) Urethane
    Vinac 884 (Air Products) Vinyl Acetate
    Dow 620 (Dow) SBR
    Airflex 4530 (Air Products) ethylene vinyl chloride
    Kymene 736 polyamido amine
    U Car Latex 651 acrylate
  • At present, it is preferred to utilize “U Car Latex 651” as the film forming latex polymer component. This is commercially available form Union Carbide and is reportedly an acrylic copolymer resin emulsion having as major latex components butyl acrylate, methyl methacrylate, and methacrylic acid polymers.
  • As to the fluoacid that is present in the treatment formulation, this is preferably a fluoacid of a Group IVB metal or mixtures thereof. Fluotitanic acid H2TiF6, is presently preferred with fluozirconic acid, H2ZrF6, also mentioned as exemplary. Combinations of these acids are also used.
  • As stated above, phosphoric acid, H3PO4, and salts thereof are also present in the treatment formulation. The phrase “phosphoric acid” used herein, refers to both the acid and salt form.
  • With regard to the non-ionic polymer surfactant, a polyoxyethylene/oxypropylene block copolymer is exemplary. The ethylene oxide (EO):propylene oxide (PO) repeat units of the copolymers may be present in a molar ratio of about 1:1-9; preferably 1:5-9; most preferably 1:9. Molecular weights of these block copolymers will range from about 2,000-4,000. These copolymers are commercially available from BASF under the “Pluronic” trademark. Presently, “Pluronic 101” is preferred for use. This specific copolymer has a ratio of EO:PO blocks of about 1:9 and a molecular weight of about 3,300.
  • Compositions in accordance with the invention are chromate free and include
    0.01-50 wt % film forming latex
    0.01-40 wt % H3PO4
    0.01-30 wt % fluoacid
    0.01-20 wt % non-ionic polymer surfactant
    wherein the weight of the composition is, in total, 100 wt %.
  • More preferred are compositions having the following range (in wt %) of the components
    1-20 wt % film forming latex
    1-50 wt % H3PO4
    1-40 wt % fluoacid
    0.01-15 wt % non-ionic polymer surfactant
    remainder water.
  • The sum of all composition components equals 100 wt %. The pH of the compositions may vary from about 1.0 to 2.0.
  • The requisite metal surface may be contacted by the treatment in spray, immersion or roller applications. The treatment is then dried and the metal surface is ready for painting or other coating applications.
  • The conversion or passivation treatment of the present invention is applied to result in a conversion coating weight of greater than about 1 milligram per square foot to treated surface with a weight of 2-150 milligrams per square foot being more preferred. For use in commercial applications, working solutions comprising about 3-100, preferably 10-100 wt % concentrations of the above “More preferred” formulation are used to contact the desired metal surfaces.
  • EXAMPLES
  • The invention will now be described in conjunction with the following examples which are to be regarded as being illustrative of certain embodiments of the invention but should not be viewed to restrict the scope of the same.
  • Example 1 Treatment Formulations
  • One tested treatment candidate formulation “A”, was a latex emulsion including the following components:
    1) U Car Latex 651 5.8 wt %
    (65% actives)
    2) H3PO4 22.0 wt % 
    3) Fluotitanic acid  10 wt %
    4) Pluronic 101 0.5 wt %
    5) Water remainder
  • U Car Latex 651 is an acrylic copolymer resin emulsion having a viscosity 20° C., cP (Brookfield, LVT #3, 50 rpm) of 400 and a particle size in microns of 0.45. It is available from the Union Carbide Corporation of Danbury, Conn. Its major constituents are 1) butyl acrylate, methyl methacrylate, methacrylic acid polymers in an amount of <65 wt %; 2) water −35%; 3) glycols, polyethylene, mono [(1,1,3,3-tetramethylbutyl)phenyl] ether in an amount of less than 2%; and 4) ammonia in 0.2 wt %. It is a white liquid.
  • Pluronic 101 is a difunctional block copolymer surfactant terminating in primary hydroxy groups and is available from BASF Corporation in Mount Olive, N.J. It is a block copolymer having hydrophobic propylene oxide (PO) repeat units and hydrophilic ethylene oxide (EtO) repeat units in a molar ratio of about 9:1. The overall molecular weight of the copolymer is about 3300.
  • Test panels for the examples were prepared as follows: G70/70 hot dipped galvanized steel test panels purchased from ACT Laboratories were spray cleaned with a 3% aqueous solution of an alkaline surfactant product and then rinsed with DI water and subsequently coated with the test treatment formulations by spin coat application, followed by forced air drying.
      • A. NSS—Neutral Salt Spray Test per ASTM B 117 and rated according to ASTM D-1654 (% white rust).
      • B. Water Resistance—ASTM D 4585—Water Resistance of Coatings Using Controlled Condensation wherein condensation is produced by exploring one surface of a coated specimen to a heated, saturated mixture of air and water vapor while the reverse side of the specimen is exposed to the cooling effect of room temperature. (% white rust).
      • C. Water Resistance of Coatings in 100% Relative Humidity according to ASTM 2247-97 (% white rust).
  • Test Results
    Test & Result
    ASTM D2247-97;
    ASTM B117/D1654 ASTM D4585 100% Rel Humidity
    Treatment 48 Hrs. NSS 240 Hrs QCT 408 hours
    A 1 0 0
    C-1 1 0 0
    C-2 100 1 10

    C-1 is a state of the art, chrome containing hexavalent chromium passivation.

    C-2 is commercially available non-chrome passivation.
  • While this invention has been described with respect to particular embodiments thereof, it is apparent that numerous other forms and modifications of this invention will be obvious to those skilled in the art. The appended claims and this invention generally should be construed to cover all such obvious forms and modifications which are within the true spirit and scope of the present invention.

Claims (21)

1. A method of forming a conversion or passivation coating on a metal surface comprising contacting said metal surface with an aqueous treatment composition comprising:
(a) a film forming latex polymer;
(b) a fluoacid;
(c) phosphoric acid; and
(d) a non-ionic polymeric surfactant.
2. A method as recited in claim 1 wherein said non-ionic polymeric surfactant comprises a polyoxyethylene/oxypropylene block copolymer.
3. A method as recited in claim 2 wherein said latex polymer comprises an acrylate resin.
4. A method as recited in claim 3 wherein acid acrylate resin comprises butyl acrylate, methyl methacrylate, and methacrylic acid polymers.
5. A method as recited in claim 2 wherein said fluoacid comprises a fluoacid of a Group IVB metal.
6. A method as recited in claim 2 wherein said polyoxyethylene/polypropylene block copolymer comprises a mole ratio of ethylene oxide (EO):propylene oxide (PO) groups of about 1:1-9.
7. A method as recited in claim 6 wherein said EO:PO molar ratio is about 1:5-9.
8. A method as recited in claim 7 wherein said polyoxyethylene/polypropylene block copolymer has a molecular weight of about 2,000-4,000.
9. A method as recited in claim 2 wherein said metal surface is a zinc covered metal surface.
10. A method as recited in claim 2 wherein said metal surface is galvanized steel.
11. A method as recited in claim 2 wherein said metal surface is aluminum.
12. A method as recited in claim 2 wherein said treatment composition is chromate free.
13. A method as recited in claim 2 further comprising drying said metal after said coating has been brought into contact with said metal, then painting said metal.
14. Composition for treating metal surfaces to form a conversion or passivation coating thereon, said composition comprising (a) a film forming latex polymer; (b) a fluoacid of a Group IVB metal; (c) phosphoric acid; and (d) a non-ionic polymeric surfactant, and water.
15. Composition for treating metal surfaces to form a conversion or passivation coating thereon, said composition comprising:
0.01-50 wt % of a film forming latex polymer;
0.01-40 wt % H3PO4;
0.01-30 wt % fluoacid;
0.01-20 wt % polyoxyethylene/oxypropylene block copolymer;
remainder water, wherein said composition equals 100 wt %.
16. Composition as recited in claim 15 wherein said composition is devoid of chromate, said polyoxyethylene/oxypropylene block copolymer comprising a mole ratio of ethylene oxide (EO):propylene oxide (PO) groups of about 1:1-9.
17. Composition as recited in claim 16 wherein said EO:PO molar ratio is about 1:5-9 and wherein said polyoxyethylene/oxypropylene block copolymer has a molecular weight of about 2,000-4,000.
18. Composition as recited in claim 17 wherein said EO:PO molar ratio is about 1:9 and said molecular weight is about 3300.
19. Composition as recited in claim 15 wherein said fluoacid comprises fluotitanic acid.
20. Composition as recited in claim 15, wherein said film forming latex polymer comprises an acrylate resin.
21. Composition as recited in claim 20 wherein said acrylate resin comprises butyl acrylate/methyl methacrylate and methacrylic acid polymers.
US10/933,014 2004-09-02 2004-09-02 Non-chrome passivation of steel Abandoned US20060042726A1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
US10/933,014 US20060042726A1 (en) 2004-09-02 2004-09-02 Non-chrome passivation of steel
MX2007002619A MX2007002619A (en) 2004-09-02 2005-08-30 Method and composition for forming a non-chrome conversion coating on steel surface.
EP05793978.7A EP1838898B1 (en) 2004-09-02 2005-08-30 Method and composition for forming a non-chrome conversion coating on steel surface
PCT/US2005/031091 WO2006028894A2 (en) 2004-09-02 2005-08-30 Method and composition for forming a non-chrome conversion coating on steel surface
CN2005800294625A CN101018888B (en) 2004-09-02 2005-08-30 Method and composition for forming a non-chrome conversion coating on steel surface
CA2578965A CA2578965C (en) 2004-09-02 2005-08-30 Method and composition for forming a non-chrome conversion coating on steel surface
ES05793978.7T ES2573537T3 (en) 2004-09-02 2005-08-30 Method and composition to form a conversion coating without chromium on a steel surface
BRPI0515626A BRPI0515626B1 (en) 2004-09-02 2005-08-30 Method and composition for forming a chrome-free conversion coating on steel surface
RU2007111918/02A RU2396370C2 (en) 2004-09-02 2005-08-30 Chromium-free passivation of steel
AU2005282751A AU2005282751B2 (en) 2004-09-02 2005-08-30 Method and composition for forming a non-chrome conversion coating on steel surface
US12/154,502 US8980015B2 (en) 2004-09-02 2008-05-23 Non-chrome passivation of steel

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Application Number Priority Date Filing Date Title
US10/933,014 US20060042726A1 (en) 2004-09-02 2004-09-02 Non-chrome passivation of steel

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EP (1) EP1838898B1 (en)
CN (1) CN101018888B (en)
AU (1) AU2005282751B2 (en)
BR (1) BRPI0515626B1 (en)
CA (1) CA2578965C (en)
ES (1) ES2573537T3 (en)
MX (1) MX2007002619A (en)
RU (1) RU2396370C2 (en)
WO (1) WO2006028894A2 (en)

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* Cited by examiner, † Cited by third party
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US20060169363A1 (en) * 2005-01-14 2006-08-03 Jasdeep Sohi Stable, non-chrome, thin-film organic passivates
WO2012045713A1 (en) * 2010-10-05 2012-04-12 Basf Se Method for passivating metallic surfaces with aqueous compositions comprising surfactants
US8986467B2 (en) 2010-10-05 2015-03-24 Basf Se Method for passivating metallic surfaces with aqueous compositions comprising surfactants
CN110054956A (en) * 2019-04-02 2019-07-26 广州市宏彩金属饰品有限公司 A kind of preparation method of the film coating agent for Treatment of Metal Surface

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101619451A (en) * 2008-07-01 2010-01-06 上海品新冶金设备有限公司 Non-chrome passivating agent for steel, zinc plates, aluminum and aluminum alloy pieces, zinc and zinc alloy
CN101619452A (en) * 2008-07-01 2010-01-06 上海品新冶金设备有限公司 Non-chrome passivating agent for steel, zinc plates, aluminum and aluminum alloy pieces, zinc and zinc alloy
DE102013107506A1 (en) * 2013-07-16 2015-01-22 Thyssenkrupp Rasselstein Gmbh Method for passivation of band-shaped black plate
CN103695888B (en) * 2013-12-24 2015-12-02 山东建筑大学 Bundy tube galvanized chromium-free olive passivation agent I
CN105154861A (en) * 2015-07-06 2015-12-16 安徽景昌铝业有限公司 Chromate-free passivation treatment process for aluminum profile material
DE102015113878B4 (en) * 2015-08-21 2023-03-16 Thyssenkrupp Ag Process for the thermal treatment of a black plate coated with a conversion layer
RU2748887C2 (en) 2016-06-22 2021-06-01 Хеметалл Гмбх Improved method for anticorrosive pretreatment of metal surfaces including steel, galvanized steel, aluminum, magnesium, and / or zinc-magnesium alloy
CN111218689A (en) * 2019-12-11 2020-06-02 陈克华 Steel surface corrosion conversion coating liquid

Citations (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2916116A (en) * 1956-09-10 1959-12-08 Television Associates Inc Control mechanism for an engine
US2926154A (en) * 1957-09-05 1960-02-23 Hercules Powder Co Ltd Cationic thermosetting polyamide-epichlorohydrin resins and process of making same
US4416729A (en) * 1982-01-04 1983-11-22 The Dow Chemical Company Ammonium polyamidoamines
US4673702A (en) * 1984-01-20 1987-06-16 Air Products And Chemicals, Inc. Stable emulsions of water resistant polyvinyl alcohol-stabilized vinyl chloride-ethylene copolymers
US4859527A (en) * 1986-05-29 1989-08-22 Air Products And Chemicals, Inc. Cellulosic nonwoven products of enhanced water and/or solvent resistance by pretreatment of the cellulosic fibers
US4962141A (en) * 1989-03-20 1990-10-09 Air Products And Chemicals, Inc. Ethylene-vinyl chloride copolymer emulsions containing tetramethylol glycoluril for use as binder compositions
US4966634A (en) * 1986-07-14 1990-10-30 Nihon Parkerizing Co., Ltd. Composition of the surface treatment for metal and the treatment method
US5120259A (en) * 1990-09-10 1992-06-09 Hirose Electric Co., Ltd. Electrical connector
US5282905A (en) * 1991-02-12 1994-02-01 Betz Laboratories, Inc. Method and composition for treatment of galvanized steel
US5298289A (en) * 1987-12-04 1994-03-29 Henkel Corporation Polyphenol compounds and treatment and after-treatment of metal, plastic and painted surfaces therewith
US5344505A (en) * 1993-08-16 1994-09-06 Betz Laboratories, Inc. Non-chromium passivation method and composition for galvanized metal surfaces
US5458698A (en) * 1987-06-01 1995-10-17 Henkel Corporation Aqueous lubricant and surface conditioner for formed metal surfaces
US5614597A (en) * 1994-12-14 1997-03-25 Hercules Incorporated Wet strength resins having reduced levels of organic halogen by-products
US5644021A (en) * 1990-12-31 1997-07-01 Hercules Incorporated Synthesis of high solids-content wet-strength resin
US5716603A (en) * 1995-06-20 1998-02-10 Eastman Chemical Company Aqueous nail polish compositions containing acrylic resins crosslinked with acrylated urethane oligomers
US5868872A (en) * 1994-04-08 1999-02-09 Henkel Kommanditgesellschaft Auf Aktien Chromium-free process for the no-rinse treatment of aluminum and its alloys and aqueous bath solutions suitable for this process
US6197880B1 (en) * 1998-04-22 2001-03-06 Sri International Method and composition for coating pre-sized paper using azetidinium and/or guanidine polymers
US6203854B1 (en) * 1997-09-17 2001-03-20 Brent International Plc Methods of and compositions for preventing corrosion of metal substrates
US6376588B1 (en) * 1991-10-15 2002-04-23 Huntsman Petrochemical Corporation Water soluble mold release composition for elastomeric compounds
US6514458B1 (en) * 2000-02-25 2003-02-04 Ge Betz, Inc. Method for removing microbes from surfaces
US20030185990A1 (en) * 2000-09-25 2003-10-02 Klaus Bittner Method for pretreating and coating metal surfaces prior to forming, with a paint-like coating and use of substrates so coated
US20040020565A1 (en) * 1999-07-08 2004-02-05 Ge Betz, Inc. Non-chromate conversion coating treatment for metals
US6758916B1 (en) * 1999-10-29 2004-07-06 Henkel Corporation Composition and process for treating metals

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4532289A (en) * 1983-11-28 1985-07-30 Sermatech International, Inc. Primer coating composition
JPH03219086A (en) * 1990-01-23 1991-09-26 Nippon Parkerizing Co Ltd Composition for metal surface treatment excellent in lubricity
AU683047B2 (en) * 1993-07-13 1997-10-30 Henkel Corporation Aqueous lubricant and surface conditioner for formed metal surfaces
CA2176332C (en) * 1993-11-16 2005-05-03 David Peter Buxton Anticorrosion treatment of metal coated steel having coatings of aluminium, zinc or alloys thereof
US6786994B2 (en) * 1996-11-04 2004-09-07 Foto-Wear, Inc. Heat-setting label sheet
DE69831351T2 (en) * 1997-10-14 2006-06-29 Henkel Kgaa Composition and method for multi-purpose treatment of metal surfaces
EP1136591A4 (en) * 1998-10-15 2005-01-12 Henkel Corp Hydrophilizing agent for metallic material, hydrophilizing fluid, method of hydrophilizing, metallic material, and heat exchanger
US6310024B1 (en) * 1999-03-26 2001-10-30 Calgon Corporation Rust and scale removal composition and process
PL202959B1 (en) * 1999-07-08 2009-08-31 Armstrong World Ind Inc Compositions for imparting desired properties to materials
JP3857866B2 (en) * 2000-02-29 2006-12-13 日本ペイント株式会社 Non-chromate metal surface treatment agent, surface treatment method and treated painted steel
DE10010758A1 (en) * 2000-03-04 2001-09-06 Henkel Kgaa Corrosion protection of zinc, aluminum and/or magnesium surfaces such as motor vehicle bodies, comprises passivation using complex fluorides of Ti, Zr, Hf, Si and/or B and organic polymers
JP4078044B2 (en) * 2001-06-26 2008-04-23 日本パーカライジング株式会社 Metal surface treatment agent, surface treatment method of metal material, and surface treatment metal material
EP1378586B1 (en) * 2002-06-13 2007-02-14 Nippon Paint Co., Ltd. Zinc phosphate-containing conditioning agent for phosphate conversion-treatment of steel plate and corresponding product

Patent Citations (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2916116A (en) * 1956-09-10 1959-12-08 Television Associates Inc Control mechanism for an engine
US2926154A (en) * 1957-09-05 1960-02-23 Hercules Powder Co Ltd Cationic thermosetting polyamide-epichlorohydrin resins and process of making same
US4416729A (en) * 1982-01-04 1983-11-22 The Dow Chemical Company Ammonium polyamidoamines
US4673702A (en) * 1984-01-20 1987-06-16 Air Products And Chemicals, Inc. Stable emulsions of water resistant polyvinyl alcohol-stabilized vinyl chloride-ethylene copolymers
US4859527A (en) * 1986-05-29 1989-08-22 Air Products And Chemicals, Inc. Cellulosic nonwoven products of enhanced water and/or solvent resistance by pretreatment of the cellulosic fibers
US4966634A (en) * 1986-07-14 1990-10-30 Nihon Parkerizing Co., Ltd. Composition of the surface treatment for metal and the treatment method
US5458698A (en) * 1987-06-01 1995-10-17 Henkel Corporation Aqueous lubricant and surface conditioner for formed metal surfaces
US5298289A (en) * 1987-12-04 1994-03-29 Henkel Corporation Polyphenol compounds and treatment and after-treatment of metal, plastic and painted surfaces therewith
US4962141A (en) * 1989-03-20 1990-10-09 Air Products And Chemicals, Inc. Ethylene-vinyl chloride copolymer emulsions containing tetramethylol glycoluril for use as binder compositions
US5120259A (en) * 1990-09-10 1992-06-09 Hirose Electric Co., Ltd. Electrical connector
US5644021A (en) * 1990-12-31 1997-07-01 Hercules Incorporated Synthesis of high solids-content wet-strength resin
US5668246A (en) * 1990-12-31 1997-09-16 Hercules Incorporated Synthesis of high solids-content wet-strength resin
US5282905A (en) * 1991-02-12 1994-02-01 Betz Laboratories, Inc. Method and composition for treatment of galvanized steel
US6376588B1 (en) * 1991-10-15 2002-04-23 Huntsman Petrochemical Corporation Water soluble mold release composition for elastomeric compounds
US5344505A (en) * 1993-08-16 1994-09-06 Betz Laboratories, Inc. Non-chromium passivation method and composition for galvanized metal surfaces
US5868872A (en) * 1994-04-08 1999-02-09 Henkel Kommanditgesellschaft Auf Aktien Chromium-free process for the no-rinse treatment of aluminum and its alloys and aqueous bath solutions suitable for this process
US5614597A (en) * 1994-12-14 1997-03-25 Hercules Incorporated Wet strength resins having reduced levels of organic halogen by-products
US5716603A (en) * 1995-06-20 1998-02-10 Eastman Chemical Company Aqueous nail polish compositions containing acrylic resins crosslinked with acrylated urethane oligomers
US6203854B1 (en) * 1997-09-17 2001-03-20 Brent International Plc Methods of and compositions for preventing corrosion of metal substrates
US6197880B1 (en) * 1998-04-22 2001-03-06 Sri International Method and composition for coating pre-sized paper using azetidinium and/or guanidine polymers
US20040020565A1 (en) * 1999-07-08 2004-02-05 Ge Betz, Inc. Non-chromate conversion coating treatment for metals
US6758916B1 (en) * 1999-10-29 2004-07-06 Henkel Corporation Composition and process for treating metals
US6514458B1 (en) * 2000-02-25 2003-02-04 Ge Betz, Inc. Method for removing microbes from surfaces
US20030185990A1 (en) * 2000-09-25 2003-10-02 Klaus Bittner Method for pretreating and coating metal surfaces prior to forming, with a paint-like coating and use of substrates so coated

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060169363A1 (en) * 2005-01-14 2006-08-03 Jasdeep Sohi Stable, non-chrome, thin-film organic passivates
WO2012045713A1 (en) * 2010-10-05 2012-04-12 Basf Se Method for passivating metallic surfaces with aqueous compositions comprising surfactants
CN103154318A (en) * 2010-10-05 2013-06-12 巴斯夫欧洲公司 Method for passivating metallic surfaces with aqueous compositions comprising surfactants
US8986467B2 (en) 2010-10-05 2015-03-24 Basf Se Method for passivating metallic surfaces with aqueous compositions comprising surfactants
CN110054956A (en) * 2019-04-02 2019-07-26 广州市宏彩金属饰品有限公司 A kind of preparation method of the film coating agent for Treatment of Metal Surface

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