EP3137652A1 - Non chromate colored conversion coating for aluminum - Google Patents

Non chromate colored conversion coating for aluminum

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Publication number
EP3137652A1
EP3137652A1 EP15722112.8A EP15722112A EP3137652A1 EP 3137652 A1 EP3137652 A1 EP 3137652A1 EP 15722112 A EP15722112 A EP 15722112A EP 3137652 A1 EP3137652 A1 EP 3137652A1
Authority
EP
European Patent Office
Prior art keywords
water
component
acidic aqueous
aqueous composition
ppm
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.)
Granted
Application number
EP15722112.8A
Other languages
German (de)
French (fr)
Other versions
EP3137652B1 (en
Inventor
Lodovico Palladini
Andrea SOLDATI
Lorenzo DERCHIA
Mathieu VAN DE CAPPELLE
Pierluigi CERIOLI
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP3137652A1 publication Critical patent/EP3137652A1/en
Application granted granted Critical
Publication of EP3137652B1 publication Critical patent/EP3137652B1/en
Active legal-status Critical Current
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C23—COATING 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
    • C23C—COATING 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
    • C23C22/00—Chemical 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
    • C23C22/05—Chemical 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
    • C23C22/06—Chemical 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
    • C23C22/40—Chemical 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 molybdates, tungstates or vanadates
    • C23C22/44—Chemical 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 molybdates, tungstates or vanadates containing also fluorides or complex fluorides
    • C—CHEMISTRY; METALLURGY
    • C23—COATING 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
    • C23C—COATING 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
    • C23C2222/00—Aspects relating to chemical surface treatment of metallic material by reaction of the surface with a reactive medium
    • C23C2222/10—Use of solutions containing trivalent chromium but free of hexavalent chromium

Definitions

  • the present invention relates to a process for the formation of colored conversion coatings on aluminum substrates using an acidic aqueous composition.
  • the invention further relates to an acidic aqueous composition that can be used in such a process and its use.
  • the present invention provides such a coating process and is based on the inventors' finding that a colored conversion coating can be formed on aluminum substrates by bringing an aluminum substrate into contact with an acidic aqueous composition comprising chromium(lll), the elements Mo and/or W, a source of fluoride, and at least one oxidizing agent having a standard reduction potential in a range from +1 ,0 to +1 ,8 V (SHE).
  • an acidic aqueous composition comprising chromium(lll), the elements Mo and/or W, a source of fluoride, and at least one oxidizing agent having a standard reduction potential in a range from +1 ,0 to +1 ,8 V (SHE).
  • the advantages of the thus produced coatings are that they allow to judge homogeneity of the product by the human eye.
  • the processes described herein provide for a corrosion resistant conversion with improved adhesion properties of organic layers which may be applied afterwards, for example in form of a paint, an adhesive layer or a protective layer, and the like.
  • no expensive and time consuming disposal of hexavalent chromium substances is needed.
  • the present invention is thus directed to a process for the formation of colored conversion coatings on aluminum substrates wherein an aluminum substrate is brought into contact with an acidic aqueous composition, comprising
  • the present invention is directed to an acidic aqueous composition
  • an acidic aqueous composition comprising a) 0.1 to 2 g/kg calculated with respect to the element Cr of at least one water-soluble compound as a source of chromium(lll),
  • the molar ratio of total fluoride of the at least one water-soluble compound according to component c) to the element Cr of the at least one water-soluble compound according to component a) is at least 3 : 1.
  • At least one refers to 1 and more, for instance 1 , 2, 3, 4, 5, 6, 7, 8, 9 or more. If this terms refers to compounds of the herein described compositions, this term does not refer to the amount of molecules, but rather to the type of compound.
  • at least one water-soluble compound as a source of chromium(lll) refers to one or more different types of water-soluble compounds as a source of chromium(lll), for example different salts. Used in combination with a given amount, the given amount is intended to cover the total amount of the respective type of constituent as described above.
  • compositions are weight percentages relative to the total weight of the composition, unless explicitly otherwise indicated. Such amounts are intended to relate to the total amount of the type of component concerned in the composition, unless otherwise indicated.
  • an amount given with respect to the "at least one water- soluble compound as a source of chromium(lll)” refers to the total amount of water-soluble compounds that can serve as a source of chromium(lll) in the composition.
  • Water-soluble refers to a solubility of at least 1 g of the respective compound in 1 kg of deionised water ( ⁇ 1 ⁇ ) at 20°C.
  • compositions used in the process of this invention are substantially free of hexavalent chromium.
  • substantially free means that the hexavalent chromium content is below 5 mol%, preferably below 1 mol%, of the total chromium content.
  • the acidic aqueous composition in a process according to the first aspect of this invention has a pH value between 0 and 7, preferably between 1 and 6, more preferably of 2,5 and 4, even more preferably of about 3.
  • the pH value may be adjusted by an acid, for example, an aqueous acid and/or by a buffer system well known to the skilled person.
  • the acids can be, without limited to, HCI, HNOs, H2SO4, and/or H3PO4, preferably H2SO4 or HNO3.
  • HNO3 can be used as component d).
  • a buffer system may be formed, for example, with a conjugated base of H3PO4 and/or ammonia.
  • the pH in the context of this invention relates to the negative logarithm to base 10 of the activity of hydronium ions at a temperature of 25 °C.
  • the aluminum substrate is brought into contact with an acidic aqueous composition with the contacting being achieved by any suitable method known in the art. Those can, for example, include spray-coating, dip-coating, spin- coating, printing and the like.
  • the contacting step can be conducted manually or automatically.
  • the aluminum substrate can be brought once or several times into contact with the acidic aqueous composition according to the present invention, for example, 1 , 2, 3, 4, 5, 6, 7, 8, 9, and more times.
  • the aluminum substrate is brought into contact with the acidic aqueous composition in an immersion or spraying process, preferably in a spraying process.
  • the contact time is at least 10 seconds, but preferably not more than 600 seconds, more preferably not more than 200 seconds.
  • the temperature of the acidic aqueous composition in a process of this invention is at least 15 °C, but preferably not higher than 80 °C, more preferably not more than 70 °C.
  • the acidic aqueous composition according to the first aspect of this invention comprises the components described above being characterized herein further.
  • the at least one water-soluble compound as a source of chromium(lll) may be any compound that is soluble in water according to the above definition.
  • the preferred source for Cr(lll) are salts of Cr(lll), including, but not limited to, chromium(lll)trifluoride (CrF3), chromium(lll)nitrate, chromium(lll)acetate, chromium(lll)gluconate and/or chromium(lll)sulfate, preferably the source is chromium(lll)trifluoride.
  • CrF3 chromium(lll)trifluoride
  • CrF3 chromium(lll)nitrate
  • chromium(lll)acetate chromium(lll)gluconate and/or chromium(lll)sulfate
  • the source is chromium(lll)trifluoride.
  • other suitable salts may also be used, all of which are
  • component a) of the acidic aqueous composition amounts to at least 10 ppm, preferably 100 ppm, more preferably more than 500 ppm, but preferably not more than 2 g/kg, more preferably not more than 1 ,5g/kg calculated with respect to the element Cr and relative to the aqueous acidic composition.
  • ppm in the context of this invention relates to "parts per million of weight", so that 1 ppm equals to 0,0001 wt.-%.
  • the at least one water-soluble compound of the element Mo and/or W according to component b) of the acidic aqueous composition may be any compound that is soluble in water according to the above definition.
  • suitable compounds include, for example and without limitation, molybdates, phosphomolybdic acid, molybdenum chloride, tungstates, such as sodium tungstate, and the like.
  • the water-soluble compound of the element Mo is a molybdate. Molybdates can be discrete or polymeric and have any suitable counterion.
  • component b) of the acidic aqueous composition amounts to at least 10 ppm, preferably to at least 20 ppm, but preferably to not more than 200 ppm, more preferably to not more than 100 ppm calculated with respect to the elements Mo and/or W and relative to the aqueous acidic composition.
  • the water-soluble compound as a source of fluoride according to component c) of the acidic aqueous composition may be selected from hydrofluoric acid, simple fluorides, such as sodium fluoride or chromium(lll)fluoride, and also complex fluoro acids, such as fluorotitanic acid or fluorozirconic acid as well as their water-soluble salts.
  • the at least one oxidizing agent which is different from the components a) to c), has a standard reduction potential in a range from +1 ,0 to +1 ,8 V (SHE).
  • This standard reduction potential refers to the commonly known standard hydrogen electrode (SHE), which is a redox electrode and the hydrogen's standard electrode potential is declared to be zero at all temperature to form a basis for comparison with all other electrode reactions.
  • An "oxidizing agent" according to compound d) of this invention preferably does not encompass dissolved oxygen or water-soluble compounds of metal elements. Accordingly, "different from the components a) to c)" means that none of the compounds a) to c) can simultaneously be considered the oxidizing agent in the sense of the present invention, but that both have to be different species.
  • the oxidizing agent is not a compound that falls within the definition of components a) to c), i.e. is no source for chromium(lll), molybdenum, tungsten, or fluoride.
  • the at least one oxidizing agent different from the components a) to c) may be, for example, HNO3 or H2O2.
  • the amount of component d) of the acidic aqueous composition is in the range of 0.01 to 1.0 g/kg, more preferably of 0.05 to 0.5 g/kg calculated on a H2O2 equivalent basis.
  • component d) is selected from water-soluble peroxides and/or oxyacids of the elements nitrogen, sulfur or chlorine as well as their water-soluble salts, preferably from hydrogen peroxide.
  • the amount of free fluoride within the acidic aqueous composition is in the range of 10 to 200 ppm and relative to the aqueous acidic composition.
  • the free fluoride content in the acidic aqueous composition in a process of this invention can be determined directly in an acidic aqueous composition of this invention by making use of a calibrated fluoride-sensitive electrode at a temperature of 25 °C.
  • the acidic aqueous composition comprises in total less than 50 ppm, more preferably less than 10 ppm of water- soluble compounds of the elements Zr and/or Ti relative to the total composition. These compounds tend to interfere with the formation of a colored conversion coating based on chromium(lll) so that their presence is less preferred.
  • the metal surfaces can be rinsed with water, for example with deionized water.
  • the metal surfaces are optionally dried after rinsing with water. If the coating with organic polymers is carried out, for example, by immersing the metal surfaces in a water-based paint dispersion, there is no need for drying after rinsing. However, if the coating based on organic polymers is an adhesive or powder coating, for example, the metal surfaces are preferably dried before this step.
  • the aluminum substrate may be provided in any shape, for example, as aluminum stripes, aluminum plates, or aluminum parts.
  • the aluminum parts treated in accordance with the invention may be joined to other metal parts through the adhesive layer.
  • the aluminum substrate in a process of this invention may be provided in any shape, for example, as aluminum stripes, aluminum plates, or aluminum parts.
  • the aluminum substrate that is brought into contact with the acidic aqueous composition according to the first aspect of this invention can be used without any pre-treatment or can be pre-treated, for example, with an alkaline cleaning solution or acidic descaling solution suitable for the inventive process. All of the pre-treatment methods and agents are well known to the skilled person.
  • the pre-treating can be conducted manually or automatically.
  • the aluminum substrate can be briefly pickled in cold concentrated nitric acid or the surfaces may be alternatively rubbed down with a squeegee.
  • the substrate can be simply rinsed with water, for example with deionized water, and may additionally be descaled with an acidic solution.
  • the solutions used for any pre-treatment may have a temperature suitable for the pre-treatment, preferably in a range from 10 to 70 °C, from 20 to 55 °C, or about 25 °C, depending on the solution and the desired effect of the solution.
  • the aluminum substrates can be pre-treated for 0.5 to 20 minutes, preferably for 1 to 10 minutes, more preferably for about 3 minutes.
  • an acidic aqueous composition that comprises
  • the molar ratio of compounds according to component a) with respect to the element Cr to compounds according to component b) with respect to the elements Mo and/or W preferably ranges from 15 : 1 to 25 : 1 , and
  • the molar ratio of total fluoride of the at least one water-soluble compound according to component c) to the element Cr of the at least one water-soluble compound according to component a) is at least 3 : 1. It is not necessary that the components a) to c) originate from different compounds. In that respect the water-soluble compound chromium(lll)fluoride is both a component a) as well as a component c). On the other hand, a compound according to component d) by definition of this invention cannot be at the same time a compound of one of the components a) to c) and is thus different from these components.
  • the molar ratio of total fluoride of the at least one water-soluble compounds according to component c) to the element Cr of the at least one water-soluble compounds according to component a) of the composition is not more than 10 : 1.
  • the total fluoride content in acidic aqueous compositions according to the second aspect of this invention can be determined as described in DIN 38 405-D-4-1 in a buffered sample volume (TISAB: "Total Ionic Strength Adjustment Buffer") taken from the acidic aqueous composition by making use of a calibrated fluoride-sensitive electrode at 25 °C sample volume temperature.
  • aluminum panels (AA6060) have been treated in order to yield colored coatings.
  • the coatings have been tested with respect to adhesion properties towards a polyester-based organic resin.
  • the pH value was 3.0 ⁇ 0.1.
  • Example E3 Conversion Coating Composition of Example E1 comprising 25 ppm Molybdenum from ammonium heptamolybdate as the source compound.
  • Example E3 Conversion Coating Composition of Example E1 comprising 25 ppm Molybdenum from ammonium heptamolybdate as the source compound.
  • Example E1 Conversion Coating Composition of Example E1 comprising 25 ppm Molybdenum from ammonium heptamolybdate as the source compound.
  • Example E1 Conversion Coating Composition of Example E1 comprising 100 ppm Molybdenum from ammonium heptamolybdate as the source compound.
  • All treated parts have been painted with a polyester powder coating (Corro-Coat PE-F series 2403, Jotun A S, Norway) and cured for 20 min at 180-190°C.

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  • 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)
  • Chemical Treatment Of Metals (AREA)

Abstract

The present invention relates to a process for the formation of colored conversion coatings on aluminum substrates using an acidic aqueous composition comprising chromium(lll), the elements Mo and/or W, a source of fluoride, and at least one oxidizing agent having a standard reduction potential in a range from +1,0 to +1,8 V (SHE). The invention further relates to an acidic aqueous composition that can be used in such a process and its use.

Description

"Non chromate colored conversion coating for aluminum"
The present invention relates to a process for the formation of colored conversion coatings on aluminum substrates using an acidic aqueous composition. The invention further relates to an acidic aqueous composition that can be used in such a process and its use.
The formation of chromium-free conversion layers on metal surfaces is covered by extensive prior art literature as cited, for example, in WO 94/28193. Such conversion layers are colorless and transparent so that the surface is bright in appearance. However, it is more desirable that the conversion coating as the result of the conversion treatment is immediately visually recognizable to the human eye. This allows to easily determine whether the process has been successfully accomplished resulting in a homogenous product. Due to the lack of color, surface analysis, for example X-ray fluorescence, is required to analyze the result of the conversion treatment process. This laborious and more time-consuming approach is the reason that hexavalent chromium based products, which are known to be carcinogenic, are still used in the architectural aluminum market.
Accordingly, there is a need for a process for the formation of colored conversion coatings on aluminum substrates using hexavalent chromium-free substances in order to avoid the usage and presence of carcinogenic substances in the process and the obtained product. The coatings thus produced should be readily and easily recognizable without the need for more laborious technical procedures.
The present invention provides such a coating process and is based on the inventors' finding that a colored conversion coating can be formed on aluminum substrates by bringing an aluminum substrate into contact with an acidic aqueous composition comprising chromium(lll), the elements Mo and/or W, a source of fluoride, and at least one oxidizing agent having a standard reduction potential in a range from +1 ,0 to +1 ,8 V (SHE).
The advantages of the thus produced coatings are that they allow to judge homogeneity of the product by the human eye. In addition, it has been found that the processes described herein provide for a corrosion resistant conversion with improved adhesion properties of organic layers which may be applied afterwards, for example in form of a paint, an adhesive layer or a protective layer, and the like. Additionally, compared to prior art compositions no expensive and time consuming disposal of hexavalent chromium substances is needed. In a first aspect, the present invention is thus directed to a process for the formation of colored conversion coatings on aluminum substrates wherein an aluminum substrate is brought into contact with an acidic aqueous composition, comprising
a) at least one water-soluble compound as a source of chromium(lll),
b) at least one water-soluble compound of the elements Mo and/or W,
c) at least one water-soluble compound as a source of fluoride,
d) at least one oxidizing agent different from the components a) to c) having a standard reduction potential in a range from +1 ,0 to +1 ,8 V (SHE).
In a second aspect, the present invention is directed to an acidic aqueous composition comprising a) 0.1 to 2 g/kg calculated with respect to the element Cr of at least one water-soluble compound as a source of chromium(lll),
b) 0.01 to 0.2 g/kg calculated with respect to the elements Mo and/or W of at least one water- soluble compound of the element Mo,
c) at least one water-soluble compound as a source of fluoride,
d) 0.01 to 1 .0 g/kg calculated on a H2O2 equivalent basis of at least one oxidizing agent different from the components a) to c) having a standard reduction potential in a range from +1.0 to +1.8 V (SHE),
wherein the molar ratio of total fluoride of the at least one water-soluble compound according to component c) to the element Cr of the at least one water-soluble compound according to component a) is at least 3 : 1.
"At least one", as used herein, refers to 1 and more, for instance 1 , 2, 3, 4, 5, 6, 7, 8, 9 or more. If this terms refers to compounds of the herein described compositions, this term does not refer to the amount of molecules, but rather to the type of compound. For example "at least one water-soluble compound as a source of chromium(lll)" refers to one or more different types of water-soluble compounds as a source of chromium(lll), for example different salts. Used in combination with a given amount, the given amount is intended to cover the total amount of the respective type of constituent as described above.
Generally, "about", as used herein, relates to ± 20 %, preferably ± 10 % of the numerical value to which it refers. "About 200" thus relates to 200 ± 40, preferably 200 ± 20.
The amounts of all components of the herein described compositions are weight percentages relative to the total weight of the composition, unless explicitly otherwise indicated. Such amounts are intended to relate to the total amount of the type of component concerned in the composition, unless otherwise indicated. For example, an amount given with respect to the "at least one water- soluble compound as a source of chromium(lll)" refers to the total amount of water-soluble compounds that can serve as a source of chromium(lll) in the composition. "Water-soluble", as used herein, refers to a solubility of at least 1 g of the respective compound in 1 kg of deionised water (κ<1 μβϋητ ) at 20°C.
The compositions used in the process of this invention are substantially free of hexavalent chromium. "Substantially free", as used in this connection, means that the hexavalent chromium content is below 5 mol%, preferably below 1 mol%, of the total chromium content.
The acidic aqueous composition in a process according to the first aspect of this invention has a pH value between 0 and 7, preferably between 1 and 6, more preferably of 2,5 and 4, even more preferably of about 3. The pH value may be adjusted by an acid, for example, an aqueous acid and/or by a buffer system well known to the skilled person. The acids can be, without limited to, HCI, HNOs, H2SO4, and/or H3PO4, preferably H2SO4 or HNO3. Furthermore, HNO3 can be used as component d). A buffer system may be formed, for example, with a conjugated base of H3PO4 and/or ammonia. The pH in the context of this invention relates to the negative logarithm to base 10 of the activity of hydronium ions at a temperature of 25 °C.
In the described process according to the first aspect of this invention, the aluminum substrate is brought into contact with an acidic aqueous composition with the contacting being achieved by any suitable method known in the art. Those can, for example, include spray-coating, dip-coating, spin- coating, printing and the like. The contacting step can be conducted manually or automatically. The aluminum substrate can be brought once or several times into contact with the acidic aqueous composition according to the present invention, for example, 1 , 2, 3, 4, 5, 6, 7, 8, 9, and more times.
In a preferred embodiment of the present invention according to the first aspect the aluminum substrate is brought into contact with the acidic aqueous composition in an immersion or spraying process, preferably in a spraying process. In a preferred embodiment the contact time is at least 10 seconds, but preferably not more than 600 seconds, more preferably not more than 200 seconds.
In a further preferred embodiment the temperature of the acidic aqueous composition in a process of this invention is at least 15 °C, but preferably not higher than 80 °C, more preferably not more than 70 °C.
The acidic aqueous composition according to the first aspect of this invention comprises the components described above being characterized herein further.
The at least one water-soluble compound as a source of chromium(lll) may be any compound that is soluble in water according to the above definition. The preferred source for Cr(lll) are salts of Cr(lll), including, but not limited to, chromium(lll)trifluoride (CrF3), chromium(lll)nitrate, chromium(lll)acetate, chromium(lll)gluconate and/or chromium(lll)sulfate, preferably the source is chromium(lll)trifluoride. Aside from those mentioned, other suitable salts may also be used, all of which are known to those skilled in the art. Examples for such salts are chromium(lll)chloride hexahydrate, chromium(lll)hydroxide, etc.
In another preferred embodiment of the first aspect of this invention, component a) of the acidic aqueous composition amounts to at least 10 ppm, preferably 100 ppm, more preferably more than 500 ppm, but preferably not more than 2 g/kg, more preferably not more than 1 ,5g/kg calculated with respect to the element Cr and relative to the aqueous acidic composition. The term "ppm" in the context of this invention relates to "parts per million of weight", so that 1 ppm equals to 0,0001 wt.-%.
The at least one water-soluble compound of the element Mo and/or W according to component b) of the acidic aqueous composition may be any compound that is soluble in water according to the above definition. Examples of suitable compounds are known to those in the art and include, for example and without limitation, molybdates, phosphomolybdic acid, molybdenum chloride, tungstates, such as sodium tungstate, and the like. In a preferred embodiment, the water-soluble compound of the element Mo is a molybdate. Molybdates can be discrete or polymeric and have any suitable counterion.
In a further preferred embodiment of the first aspect of this invention, component b) of the acidic aqueous composition amounts to at least 10 ppm, preferably to at least 20 ppm, but preferably to not more than 200 ppm, more preferably to not more than 100 ppm calculated with respect to the elements Mo and/or W and relative to the aqueous acidic composition.
The water-soluble compound as a source of fluoride according to component c) of the acidic aqueous composition may be selected from hydrofluoric acid, simple fluorides, such as sodium fluoride or chromium(lll)fluoride, and also complex fluoro acids, such as fluorotitanic acid or fluorozirconic acid as well as their water-soluble salts.
The at least one oxidizing agent, which is different from the components a) to c), has a standard reduction potential in a range from +1 ,0 to +1 ,8 V (SHE). This standard reduction potential refers to the commonly known standard hydrogen electrode (SHE), which is a redox electrode and the hydrogen's standard electrode potential is declared to be zero at all temperature to form a basis for comparison with all other electrode reactions. An "oxidizing agent" according to compound d) of this invention preferably does not encompass dissolved oxygen or water-soluble compounds of metal elements. Accordingly, "different from the components a) to c)" means that none of the compounds a) to c) can simultaneously be considered the oxidizing agent in the sense of the present invention, but that both have to be different species. In other words, this does also mean that the oxidizing agent is not a compound that falls within the definition of components a) to c), i.e. is no source for chromium(lll), molybdenum, tungsten, or fluoride. The at least one oxidizing agent different from the components a) to c) may be, for example, HNO3 or H2O2.
In a preferred embodiment of the first aspect of this invention, the amount of component d) of the acidic aqueous composition is in the range of 0.01 to 1.0 g/kg, more preferably of 0.05 to 0.5 g/kg calculated on a H2O2 equivalent basis.
In a further preferred embodiment component d) is selected from water-soluble peroxides and/or oxyacids of the elements nitrogen, sulfur or chlorine as well as their water-soluble salts, preferably from hydrogen peroxide.
In yet another preferred embodiment of the first aspect of this invention, the amount of free fluoride within the acidic aqueous composition is in the range of 10 to 200 ppm and relative to the aqueous acidic composition. The free fluoride content in the acidic aqueous composition in a process of this invention can be determined directly in an acidic aqueous composition of this invention by making use of a calibrated fluoride-sensitive electrode at a temperature of 25 °C.
In a further preferred embodiment of the first aspect of this invention, the acidic aqueous composition comprises in total less than 50 ppm, more preferably less than 10 ppm of water- soluble compounds of the elements Zr and/or Ti relative to the total composition. These compounds tend to interfere with the formation of a colored conversion coating based on chromium(lll) so that their presence is less preferred.
After contacting with the acidic aqueous composition described herein, the metal surfaces can be rinsed with water, for example with deionized water. Depending on the nature of the subsequent coating with organic polymers, the metal surfaces are optionally dried after rinsing with water. If the coating with organic polymers is carried out, for example, by immersing the metal surfaces in a water-based paint dispersion, there is no need for drying after rinsing. However, if the coating based on organic polymers is an adhesive or powder coating, for example, the metal surfaces are preferably dried before this step.
The aluminum substrate may be provided in any shape, for example, as aluminum stripes, aluminum plates, or aluminum parts. The aluminum parts treated in accordance with the invention may be joined to other metal parts through the adhesive layer.
The aluminum substrate in a process of this invention may be provided in any shape, for example, as aluminum stripes, aluminum plates, or aluminum parts. The aluminum substrate that is brought into contact with the acidic aqueous composition according to the first aspect of this invention, can be used without any pre-treatment or can be pre-treated, for example, with an alkaline cleaning solution or acidic descaling solution suitable for the inventive process. All of the pre-treatment methods and agents are well known to the skilled person. The pre-treating can be conducted manually or automatically. For example, the aluminum substrate can be briefly pickled in cold concentrated nitric acid or the surfaces may be alternatively rubbed down with a squeegee. Optionally, the substrate can be simply rinsed with water, for example with deionized water, and may additionally be descaled with an acidic solution. These treatments may be used separately or in combination. The solutions used for any pre-treatment may have a temperature suitable for the pre-treatment, preferably in a range from 10 to 70 °C, from 20 to 55 °C, or about 25 °C, depending on the solution and the desired effect of the solution. Furthermore, the aluminum substrates can be pre-treated for 0.5 to 20 minutes, preferably for 1 to 10 minutes, more preferably for about 3 minutes.
According to the second aspect of this invention an acidic aqueous composition is encompassed that comprises
a) 0.1 to 2 g/kg calculated with respect to the element Cr of at least one water-soluble compound as a source of chromium(lll),
b) 0.01 to 0.2 g/kg calculated with respect to the elements Mo and/or W of at least one water- soluble compound of the element Mo,
c) at least one water-soluble compound as a source of fluoride,
d) 0.01 to 1 .0 g/kg calculated on a H2O2 equivalent basis of at least one oxidizing agent different from the components a) to c) having a standard reduction potential in a range from + 1.0 to +1.8 V (SHE),
wherein the molar ratio of compounds according to component a) with respect to the element Cr to compounds according to component b) with respect to the elements Mo and/or W preferably ranges from 15 : 1 to 25 : 1 , and
wherein the molar ratio of total fluoride of the at least one water-soluble compound according to component c) to the element Cr of the at least one water-soluble compound according to component a) is at least 3 : 1. It is not necessary that the components a) to c) originate from different compounds. In that respect the water-soluble compound chromium(lll)fluoride is both a component a) as well as a component c). On the other hand, a compound according to component d) by definition of this invention cannot be at the same time a compound of one of the components a) to c) and is thus different from these components.
In a preferred embodiment the molar ratio of total fluoride of the at least one water-soluble compounds according to component c) to the element Cr of the at least one water-soluble compounds according to component a) of the composition is not more than 10 : 1. The total fluoride content in acidic aqueous compositions according to the second aspect of this invention can be determined as described in DIN 38 405-D-4-1 in a buffered sample volume (TISAB: "Total Ionic Strength Adjustment Buffer") taken from the acidic aqueous composition by making use of a calibrated fluoride-sensitive electrode at 25 °C sample volume temperature.
All embodiments described herein with relation to the process of this invention are equally applicable to the compositions defining the second aspect of this invention and vice versa. This especially means that all preferred embodiments disclosed herein in relation to the compositions used in the described processes and thus in the context of the first aspect of this invention apply similarly to the described compositions.
Examples
Within a process sequence as listed below aluminum panels (AA6060) have been treated in order to yield colored coatings. The coatings have been tested with respect to adhesion properties towards a polyester-based organic resin.
Cycle:
1. Alkaline Cleaning (Ridoline G 34 A (3,5 %), 55 °C, 3 min)
2. Rinse
3. Acidic Etching (Grametal DX 255 A (3 %), 25 °C, 3 min)
4. Rinse
5. Dl rinse
6. Conversion Coating Treatment (35 °C, 45 sec, Spraying Pressure: 1 atm)
7. Dl rinse
According to the above-mentioned process sequence the aluminum panels had been treated while the conversion treatment was performed through making use of the following different conversion coating compositions.
Comparative Example CE1 :
34 ppm Ti from H2T1F6 as source compound
56 ppm Maleic Acid - Methylvinylether Copolymer
35 ppm Polyvinylalcohol
The pH value was 3.0 ± 0.1.
Comparative Example CE2:
Conversion Coating Composition of Comparative Example CE2 comprising additionally 25 ppm Molybdenum from ammonium heptamolybdate as the source compound.
Example E1 :
1 ,06 g/kg Cr(lll) from CrF3 as source compound
66 ppm Zr from hhZrFe as source compound
12 ppm Mo from (NH4)6Mo7024 ■ 4 H20
An amount of HNO3 to adjust the pH value to 3.0.
Example E2:
Conversion Coating Composition of Example E1 comprising 25 ppm Molybdenum from ammonium heptamolybdate as the source compound. Example E3:
Conversion Coating Composition of Example E1 comprising 25 ppm Molybdenum from ammonium heptamolybdate as the source compound.
Example E4:
Conversion Coating Composition of Example E1 comprising 100 ppm Molybdenum from ammonium heptamolybdate as the source compound.
All treated parts have been painted with a polyester powder coating (Corro-Coat PE-F series 2403, Jotun A S, Norway) and cured for 20 min at 180-190°C.
Results in the Wet Adhesion Test are summarized in Table 1 and reveal that the examples according to the invention (E1-E4) adhere sufficiently to the aluminum panel and are superior to chromium-free compositions independent of the additional presence of molybdenum (CE1 , CE2).
The visibility of Cr(lll)-Mo conversion coating (E1-E4) starts with 12 mg/kg Mo and increases fast with further additions. 25-50 mg/kg Mo gives a very good color that appears to be ideal for real life application. Color intensity is similar to Ti-Mo technology (CE2).

Claims

Claims
1. Process for the formation of colored conversion coatings on aluminum substrates wherein an aluminum substrate is brought into contact with an acidic aqueous composition comprising
a) at least one water-soluble compound as a source of chromium(lll),
b) at least one water-soluble compound of the elements Mo and/or W,
c) at least one water-soluble compound as a source of fluoride,
d) at least one oxidizing agent different from the components a) to c) having a
standard reduction potential in a range from +1.0 to +1.8 V (SHE).
2. Process according to claim 1 wherein component a) of the acidic aqueous composition amounts to at least 100 ppm, preferably at least 500 ppm, but preferably to not more than 2 g/kg, more preferably not more than 1 ,5 g/kg calculated with respect to the element Cr.
3. Process according to any one of the preceding claims wherein component a) is selected from chromium(lll)trifluoride, chromium(lll)nitrate and/or chromium(lll)sulfate, preferably from chromium(lll)trifluoride.
4. Process according to any one of the preceding claims wherein component b) of the acidic aqueous composition amounts to at least 10 ppm, preferably to at least 20 ppm, but preferably to not more than 200 ppm, more preferably to not more than 100 ppm calculated with respect to the elements Mo and/or W.
5. Process according to any one of the preceding claims wherein component b) is selected from water-soluble compounds of the element Mo, preferably from molybdates.
6. Process according to any one of the preceding claims wherein the amount of free fluoride within the acidic aqueous composition is in the range of 10 to 200 ppm.
7. Process according to any one of the preceding claims wherein the amount of component d) of the acidic aqueous composition is in the range of 0.01 to 1.0 g/kg, preferably of 0.05 to 0.5 g/kg calculated on a H2O2 equivalent basis.
8. Process according to any one of the preceding claims wherein component d) is selected from water-soluble peroxides and/or oxyacids of the elements nitrogen, sulfur or chlorine, preferably from hydrogen peroxide and/or nitrate ions, more preferably from hydrogen peroxide.
9. Process according to any one of the preceding claims wherein the acidic aqueous composition comprises in total less than 50 ppm of water-soluble compounds of the elements Zr and/or Ti.
10. Process according to any one of the preceding claims wherein the aluminum substrate is brought into contact with the acidic aqueous composition through an immersion or spraying process, preferably through an immersion process.
1 1. Process according to claim 10 wherein the contact time for the immersion process is at least 10 seconds, but preferably not more than 200 seconds.
12. Process according to claim 1 1 wherein the temperature of the acidic aqueous composition is at least 15 °C, but preferably not higher than 50 °C.
13. Acidic aqueous composition comprising
a) 0.1 to 2 g/kg calculated with respect to the element Cr of at least one water-soluble compound as a source of chromium(lll),
b) 0.01 to 0.2 g/kg calculated with respect to the elements Mo and/or W of at least one water-soluble compound of the element Mo,
c) at least one water-soluble compound as a source of fluoride,
d) 0.01 to 1.0 g/kg calculated on a H2O2 equivalent basis of at least one oxidizing agent different from the components a) to c) having a standard reduction potential in a range from +1.0 to +1.8 V (SHE),
wherein the molar ratio of total fluoride of the at least one water-soluble compound according to component c) to the element Cr of the at least one water-soluble compound according to component a) is at least 3 : 1.
14. Composition according to claim 13 wherein the molar ratio of total fluoride of the at least one water-soluble compound according to component c) to the element Cr of the at least one water-soluble compound according to component a) is not more than 10 : 1 .
15. Composition according to one or both of the claims 13 to 14 wherein the molar ratio of compounds according to component a) with respect to the element Cr to compounds according to component b) with respect to the elements Mo and/or W ranges from 15 : 1 to 25 : 1 , and
EP15722112.8A 2014-05-01 2015-04-29 Non chromate colored conversion coating for aluminum Active EP3137652B1 (en)

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GBGB1407690.5A GB201407690D0 (en) 2014-05-01 2014-05-01 Non chromate coloured conversion coating for aluminum
PCT/EP2015/059322 WO2015165956A1 (en) 2014-05-01 2015-04-29 Non chromate colored conversion coating for aluminum

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FR3073529B1 (en) * 2017-11-14 2021-07-02 Mecaprotec Ind PROCESS FOR SURFACE TREATMENT OF A PART COATED WITH A CADMIUM COATING AND COMPOSITION FOR THE IMPLEMENTATION OF SUCH A PROCESS
CN110983411A (en) * 2020-01-07 2020-04-10 昆明理工大学 A kind of preparation method of natural color conversion film on aluminum alloy surface

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CA1228000A (en) * 1981-04-16 1987-10-13 David E. Crotty Chromium appearance passivate solution and process
RO113063B1 (en) * 1997-03-24 1998-03-30 Inst Cercetare Si Proiectare T Low-pollution solution for colourless-bluish passivation of electrochemical zinc and zinc alloy deposits
US7402214B2 (en) * 2002-04-29 2008-07-22 Ppg Industries Ohio, Inc. Conversion coatings including alkaline earth metal fluoride complexes
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US20070243397A1 (en) * 2006-04-17 2007-10-18 Ludwig Robert J Chromium(VI)-free, aqueous acidic chromium(III) conversion solutions
CN1858303B (en) * 2006-06-09 2010-07-21 广东多正化工科技有限公司 Normal temperature passivated zinc coating trivalent chromium color passivating agent
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TW201602410A (en) 2016-01-16
CN106232872A (en) 2016-12-14
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WO2015165956A1 (en) 2015-11-05
GB201407690D0 (en) 2014-06-18
CN106232872B (en) 2019-04-23

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