EP3243928A1 - Conversion coating treatment - Google Patents

Conversion coating treatment Download PDF

Info

Publication number
EP3243928A1
EP3243928A1 EP17170451.3A EP17170451A EP3243928A1 EP 3243928 A1 EP3243928 A1 EP 3243928A1 EP 17170451 A EP17170451 A EP 17170451A EP 3243928 A1 EP3243928 A1 EP 3243928A1
Authority
EP
European Patent Office
Prior art keywords
composition
substrate
container
chamber
kit
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP17170451.3A
Other languages
German (de)
French (fr)
Inventor
Blair Smith
Mark R. Jaworowski
Weilong Zhang
Michael A. Kryzman
Bart Antonie Van Hassel
Georgios S. Zafiris
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.)
Hamilton Sundstrand Corp
Original Assignee
Hamilton Sundstrand Corp
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 Hamilton Sundstrand Corp filed Critical Hamilton Sundstrand Corp
Publication of EP3243928A1 publication Critical patent/EP3243928A1/en
Withdrawn legal-status Critical Current

Links

Images

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
    • C23C22/82After-treatment
    • C23C22/83Chemical after-treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B43WRITING OR DRAWING IMPLEMENTS; BUREAU ACCESSORIES
    • B43KIMPLEMENTS FOR WRITING OR DRAWING
    • B43K5/00Pens with ink reservoirs in holders, e.g. fountain-pens
    • B43K5/18Arrangements for feeding the ink to the nibs
    • B43K5/1818Mechanical feeding means, e.g. valves; Pumps
    • B43K5/1827Valves
    • B43K5/1836Valves automatically closing
    • B43K5/1845Valves automatically closing opened by actuation of the writing point
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B43WRITING OR DRAWING IMPLEMENTS; BUREAU ACCESSORIES
    • B43MBUREAU ACCESSORIES NOT OTHERWISE PROVIDED FOR
    • B43M11/00Hand or desk devices of the office or personal type for applying liquid, other than ink, by contact to surfaces, e.g. for applying adhesive
    • B43M11/06Hand-held devices
    • B43M11/08Hand-held devices of the fountain-pen type
    • 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
    • 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
    • C23C22/73Chemical 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 characterised by the process
    • 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
    • C23C2222/00Aspects relating to chemical surface treatment of metallic material by reaction of the surface with a reactive medium
    • C23C2222/10Use of solutions containing trivalent chromium but free of hexavalent chromium

Definitions

  • This disclosure relates to coatings for corrosion protection, and more specifically to conversion coatings for corrosion protection of metal substrates.
  • conversion coatings have been used to protect metals such as aluminum, zinc, cadmium, tin, magnesium, iron, copper, silver, and their alloys such as zinc-nickel, tin-zinc, etc.
  • Conversion coating compositions have been commonly applied to large surface area substrates by immersion or spray application. Such techniques, however, can be cumbersome for touch-up application such as to repair abraded surfaces or at connection interfaces between assembled metal components.
  • Small scale handheld application of conversion coatings has been performed with felt pen-style applicators.
  • chromate conversion coatings utilizing hexavalent chromium have been effectively used to provide corrosion protection. However, the use of hexavalent chromium is largely in the process of being discontinued due to toxicity concerns.
  • Touch-up conversion coatings based on trivalent chromium have been applied with felt pen-style applicators; however, such trivalent conversion coatings have been found to be less effective at preventing corrosion than conversion coatings based on hexavalent chromium.
  • a kit for applying a coating comprises a first handheld container comprises a first liquid composition disposed therein that comprises a trivalent chromium salt.
  • a first applicator is disposed in fluid communication with the first container and is configured to dispense the first composition.
  • the kit also includes a second handheld container comprises a second liquid composition disposed therein comprising an oxidizing agent.
  • a second applicator is disposed in fluid communication with the second container and is configured to dispense the second composition.
  • a method of using the above-described kit comprises applying a coating of the first composition to a substrate, allowing a drying period of time to pass, applying the second composition to the coated substrate, and maintaining a wet layer of the second composition on the coated substrate for at least 0.5 minutes.
  • a method of protecting a trivalent chromium conversion-coated substrate from corrosion comprises contacting the substrate with a porous pad disposed on an end of an oblong handheld housing in fluid communication with a chamber disposed within the housing, and dispensing a liquid composition comprising an oxidizing agent disposed in the chamber onto the substrate through the porous pad.
  • FIG. 1 schematically depicts an example embodiment of a kit for applying a conversion coating.
  • a first container in the form of housing 10a has a liquid composition comprising a trivalent chromium salt disposed in chamber 11a formed by the housing 10a and barrier 12a.
  • a second container in the form of housing 10b has a liquid composition comprising an oxidizing agent disposed in chamber 11b formed by the housing 10b and barrier 12b.
  • the housings 10a and 10b can be configured in various shapes, sizes, and forms in order to facilitate being held by hand during use. In some embodiments, the housings are configured in an oblong configuration as depicted in FIG. 1 .
  • an oblong housing can have a maximum linear dimension in a cross-sectional plane perpendicular to the longest oblong axis in ranges having a lower endpoint of 5 mm, more specifically 10 mm, and even more specifically 15 mm, and an upper endpoint of 50 mm, more specifically 40 mm, more specifically 30 mm, and even more specifically 25 mm.
  • an oblong housing can be configured as a cylinder. Such embodiments can also be referred to as a "coating pen” or "coating pens”.
  • the cylinder can have a diameter in ranges having a lower endpoint of 5 mm, more specifically 10 mm, and even more specifically 15 mm, and an upper endpoint of 50 mm, more specifically of 40 mm, more specifically 30 mm, and even more specifically 25 mm.
  • the above upper and lower endpoints can be independently combined to disclose various different ranges.
  • the trivalent chromium salt composition can be an aqueous solution or a non-aqueous solution comprising trivalent chromium and various anions.
  • exemplary anions include nitrate, sulfate, phosphate, and/or acetate.
  • Specific exemplary trivalent chromium salts can include Cr 2 (SO 4 ) 3 , (NH) 4 Cr(SO 4 ) 2 , KCr(SO 4 ) 2 , CrF 3 Cr(NO3) 3 , and mixtures comprising any of the foregoing.
  • the concentration of the trivalent chromium salt in the composition, per liter of solution, can range from about 0.01 g to about 22 g, more specifically from about 3 g to about 12 g, and even more specifically from about 4 g to about 8.0 g.
  • concentration of the trivalent chromium salt in the composition can range from about 0.01 g to about 22 g, more specifically from about 3 g to about 12 g, and even more specifically from about 4 g to about 8.0 g.
  • Embodiments of compositions and the application thereof to substrates are described in US Patent Nos. 5,304,257 , 5,374,347 , 6,375,726 , 6,511,532 , 6,521,029 , and 6,511,532 .
  • Various additives and other materials can be included in the composition comprising trivalent chromium as disclosed in the patent literature, and the trivalent chromium salt composition can be selected from any of a number of known commercially-available compositions.
  • the oxidizing agent can be a peroxide or a permanganate salt.
  • the oxidizing agent is hydrogen peroxide (H 2 O 2 ).
  • peroxides other than hydrogen peroxide include inorganic peroxides (e.g. Li 2 O 2 , Na 2 O 2 , K 2 O 2 , BaO 2 ), and organic peroxides (e.g., R-OO-R', R-OO-H, or RCO-OO-R', where R, and R' are organic groups).
  • the oxidizing agent can be in aqueous or non-aqueous solutions at concentrations in ranges having a lower endpoint of 0.1 wt.%, more specifically 0.5 wt.%, more specifically 1.0 wt.%, more specifically 2.0 wt.%, more specifically 3.0 wt.%, and more specifically 4.0 wt.%, and an upper endpoint of 10.0 wt.%, more specifically 9.0 wt.%, more specifically 8 wt.%, more specifically 7 wt.%, more specifically 6 wt.%, more specifically 4 wt.%, and even more specifically 3.5 wt.%.
  • the above upper and lower endpoints can be independently combined to disclose various different ranges.
  • compositions in the chambers 11a, 11b can be dispensed by bringing the liquid compositions in the chambers 11a, 11b into contact with the dispensing applicators 14a, 14b, respectively.
  • Each dispensing applicator 14a, 14b can independently be selected as a porous material configured to transport the liquid composition from the respective chamber 11a, 11b to a substrate in contact with the outer surface of the applicator 14a, 14b.
  • the liquid composition can be brought into contact with the applicator 14a, 14b by bringing the dispensing applicator 14a, 14b into contact with a fixed-position surface (which can but does not have to be the substrate to be coated) and applying hand pressure on the housing 10a, 10b toward the surface to open the poppet valve 15a, 15b.
  • the dispensing applicators 14a, 14b are slideably mounted in the housing 10a, 10b. At rest, the dispensing applicators 14a, 14b are biased away from the main body of the housing 10a, 10b by applicator biasing members (not shown) to an at-rest position as shown in FIG. 1 .
  • This biasing force is transmitted through actuator 16a, 16b to apply an expansive force on the spring member 18a, 18b, which intern acts on the poppet valve 15a, 15b to keep it engaged on the barrier 12a, 12b and closed.
  • actuator 16a, 16b Upon the application of hand pressure urging housing 10a, 10b toward the surface, the counteracting force of the surface acting on the dispensing each applicator 14a, 14b compresses the spring member 18a, 18b until the fully compressed spring and actuator engage against the poppet valve 15a, 15b and displace it away from the barrier 12a, 12b to open the poppet valve 15a, 15b.
  • Hand pressure can be maintained to keep the poppet valve open for a period of time sufficient to charge a desired quantity of liquid into chamber 17a, 17b, at which point the hand pressure can be removed or relaxed so that the applicator biasing members again bias the applicators 14a, 14b to the at-rest position with the poppet valve 15a, 15b closed. Liquid in the chamber 17a, 17b can then continue to be delivered and spread on the substrate.
  • the applicators 14a, 14b are not limited to porous pads.
  • the applicators 14a, 14b could also be independently selected from brushes, rollers, nozzles, etc. When not in use, the applicators 14a, 14b can be covered with an air- and liquid-tight cap.
  • FIG. 2 Another example embodiment of a kit is schematically depicted in FIG. 2 , in which the first and second containers are configured as first and second chambers 11a, 11b formed by housing 10 and barrier 20, with applicators 14a, 14b disposed at opposing ends of the oblong or cylindrical housing 10.
  • the remaining components and features depicted in FIG. 2 and their operation are as in FIG. 1 , and do not require further explanation.
  • the embodiment depicted in FIG. 2 provides additional technical benefits of convenience and efficiency, while reducing the potential for cross-contamination between the compositions by delivering the two distinct chemical compositions through applicators disposed on opposite ends of a coating pen.
  • the applicator 14b can be formed from a material that is resistant to wicking of material from the coated substrate into the chamber 17b from which it could potentially infiltrate to the chamber 11b when the poppet valve 15b is open. Such materials can include surfaces that are resistant to wetting by the coated chromium salt composition.
  • the poppet valve 15b can include check-valve features (not shown, but known in the valve art) to prevent migration of fluid from chamber 17b into chamber 11b.
  • anti-contamination procedures can be followed such as draining or flushing the chamber 17b after application is complete, or using a surface other than the coated substrate for displacing the applicator 14b to charge the chamber 17b so that the poppet valve 15b is closed before the applicator 14b comes into contact with the coated substrate. Combinations of the above materials or procedures can be used as well.
  • the first liquid composition comprising the trivalent chromium salt can be allowed to contact the substrate for a period of time before applying the second composition comprising the oxidizing agent, and in some embodiments the kit can include instructions to that effect.
  • the amount of contact time can vary considerably depending on the ambient temperature and humidity, the specific properties of the applicator and the liquid composition, and the thickness with which it is applied. Any amount of contact time greater than zero can be used. In some embodiments, contact times can range from 1 minute to 5 minutes. In some embodiments, contact times can range from 1 minute to 3 minutes.
  • a wet layer of the second liquid composition comprising the oxidizing agent is maintained on the coated substrate for a minimum period of time.
  • minimum wet layer time limits can include 0.5 minutes, more specifically 1 minute, more specifically 1.5 minutes, more specifically 2 minutes, more specifically 3 minutes, more specifically 4 minutes, and even more specifically 5 minutes. Theoretically there is no maximum wet layer time; however, minimization of the opportunity costs of lost efficiency typically results in drying times that do not drastically exceed the specified minimum wet layer time.
  • a wet layer of the second liquid composition comprising the oxidizing agent is maintained by making a plurality of passes over the substrate with the applicator 14b, and in some embodiments the kit can include instructions to that effect.
  • the second liquid composition can be configured to maintain a wet layer for a target duration, e.g., through the inclusion of additives such as gel or thickening agents (e.g., fused silica, water soluble polymers) or lower volatility solvents.
  • Moisture can also be retained by film-forming agents in the first composition such as sodium or potassium salts of hexafluorotitanic acid or hexafluorozirconic acid, or the selection of a chromium salt with colligative properties such as high solubility that render it inherently slow-drying.
  • film-forming agents in the first composition such as sodium or potassium salts of hexafluorotitanic acid or hexafluorozirconic acid, or the selection of a chromium salt with colligative properties such as high solubility that render it inherently slow-drying.

Abstract

A kit for applying a coating includes a first handheld container (10a) with a first liquid trivalent chromium salt composition disposed therein. A first applicator (14a) is disposed in fluid communication with the first container and is configured to dispense the first composition. The kit also includes a second handheld container (10b) having a second liquid oxidizing agent composition disposed therein. A second applicator (14b) is disposed in fluid communication with the second container and is configured to dispense the second composition.

Description

    BACKGROUND
  • This disclosure relates to coatings for corrosion protection, and more specifically to conversion coatings for corrosion protection of metal substrates.
  • Many metals are subject to corrosion, which can be exacerbated by exposure to corrosion-promoting environmental conditions such as high-chloride environments found in proximity to marine environments. Surface coatings have been used to provide protection against corrosion by imposing a physical barrier between the metal substrate and the surrounding environment. However, conventional polymer surface coatings can suffer from a number of problems such as inadequate or uneven thickness, pinholes and other gaps in coating coverage, and the necessity of extensive surface preparation of the substrate prior to application of the coating in order to provide adequate bonding between the coating and the substrate, in addition to the cost, time and complexity of applying the polymer coating.
  • Metal surface treatments such as conversion coatings have been used to protect metals such as aluminum, zinc, cadmium, tin, magnesium, iron, copper, silver, and their alloys such as zinc-nickel, tin-zinc, etc. Conversion coating compositions have been commonly applied to large surface area substrates by immersion or spray application. Such techniques, however, can be cumbersome for touch-up application such as to repair abraded surfaces or at connection interfaces between assembled metal components. Small scale handheld application of conversion coatings has been performed with felt pen-style applicators. Historically, chromate conversion coatings utilizing hexavalent chromium have been effectively used to provide corrosion protection. However, the use of hexavalent chromium is largely in the process of being discontinued due to toxicity concerns. Touch-up conversion coatings based on trivalent chromium have been applied with felt pen-style applicators; however, such trivalent conversion coatings have been found to be less effective at preventing corrosion than conversion coatings based on hexavalent chromium.
  • BRIEF DESCRIPTION
  • According to some aspects of this disclosure, a kit for applying a coating comprises a first handheld container comprises a first liquid composition disposed therein that comprises a trivalent chromium salt. A first applicator is disposed in fluid communication with the first container and is configured to dispense the first composition. The kit also includes a second handheld container comprises a second liquid composition disposed therein comprising an oxidizing agent. A second applicator is disposed in fluid communication with the second container and is configured to dispense the second composition.
  • In some aspects, a method of using the above-described kit comprises applying a coating of the first composition to a substrate, allowing a drying period of time to pass, applying the second composition to the coated substrate, and maintaining a wet layer of the second composition on the coated substrate for at least 0.5 minutes.
  • In some aspects, a method of protecting a trivalent chromium conversion-coated substrate from corrosion comprises contacting the substrate with a porous pad disposed on an end of an oblong handheld housing in fluid communication with a chamber disposed within the housing, and dispensing a liquid composition comprising an oxidizing agent disposed in the chamber onto the substrate through the porous pad.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The subject matter which is regarded as the present disclosure is particularly pointed out and distinctly claimed in the claims at the conclusion of the specification. The foregoing and other features, and advantages of the present disclosure are apparent from the following detailed description taken in conjunction with the accompanying drawings in which:
    • FIG. 1 is a schematic depiction of a cross-sectional view of an example embodiment of a kit for applying a conversion coating; and
    • FIG. 2 is a schematic depiction of a cross-sectional view of another example embodiment of a kit for applying a conversion coating.
    DETAILED DESCRIPTION
  • With reference now to the Figures, FIG. 1 schematically depicts an example embodiment of a kit for applying a conversion coating. As shown in FIG. 1, a first container in the form of housing 10a has a liquid composition comprising a trivalent chromium salt disposed in chamber 11a formed by the housing 10a and barrier 12a. A second container in the form of housing 10b has a liquid composition comprising an oxidizing agent disposed in chamber 11b formed by the housing 10b and barrier 12b. The housings 10a and 10b can be configured in various shapes, sizes, and forms in order to facilitate being held by hand during use. In some embodiments, the housings are configured in an oblong configuration as depicted in FIG. 1. In some embodiments, an oblong housing can have a maximum linear dimension in a cross-sectional plane perpendicular to the longest oblong axis in ranges having a lower endpoint of 5 mm, more specifically 10 mm, and even more specifically 15 mm, and an upper endpoint of 50 mm, more specifically 40 mm, more specifically 30 mm, and even more specifically 25 mm. In some embodiments, an oblong housing can be configured as a cylinder. Such embodiments can also be referred to as a "coating pen" or "coating pens". In some embodiments, the cylinder can have a diameter in ranges having a lower endpoint of 5 mm, more specifically 10 mm, and even more specifically 15 mm, and an upper endpoint of 50 mm, more specifically of 40 mm, more specifically 30 mm, and even more specifically 25 mm. The above upper and lower endpoints can be independently combined to disclose various different ranges.
  • In some embodiments, the trivalent chromium salt composition can be an aqueous solution or a non-aqueous solution comprising trivalent chromium and various anions. Exemplary anions include nitrate, sulfate, phosphate, and/or acetate. Specific exemplary trivalent chromium salts can include Cr2(SO4)3, (NH)4Cr(SO4)2, KCr(SO4)2, CrF3 Cr(NO3)3, and mixtures comprising any of the foregoing. The concentration of the trivalent chromium salt in the composition, per liter of solution, can range from about 0.01 g to about 22 g, more specifically from about 3 g to about 12 g, and even more specifically from about 4 g to about 8.0 g. Embodiments of compositions and the application thereof to substrates are described in US Patent Nos. 5,304,257 , 5,374,347 , 6,375,726 , 6,511,532 , 6,521,029 , and 6,511,532 . Various additives and other materials can be included in the composition comprising trivalent chromium as disclosed in the patent literature, and the trivalent chromium salt composition can be selected from any of a number of known commercially-available compositions.
  • In some embodiments, the oxidizing agent can be a peroxide or a permanganate salt. In some embodiments, the oxidizing agent is hydrogen peroxide (H2O2). Examples of peroxides other than hydrogen peroxide include inorganic peroxides (e.g. Li2O2, Na2O2, K2O2, BaO2), and organic peroxides (e.g., R-OO-R', R-OO-H, or RCO-OO-R', where R, and R' are organic groups). The oxidizing agent can be in aqueous or non-aqueous solutions at concentrations in ranges having a lower endpoint of 0.1 wt.%, more specifically 0.5 wt.%, more specifically 1.0 wt.%, more specifically 2.0 wt.%, more specifically 3.0 wt.%, and more specifically 4.0 wt.%, and an upper endpoint of 10.0 wt.%, more specifically 9.0 wt.%, more specifically 8 wt.%, more specifically 7 wt.%, more specifically 6 wt.%, more specifically 4 wt.%, and even more specifically 3.5 wt.%. The above upper and lower endpoints can be independently combined to disclose various different ranges.
  • The compositions in the chambers 11a, 11b can be dispensed by bringing the liquid compositions in the chambers 11a, 11b into contact with the dispensing applicators 14a, 14b, respectively. Each dispensing applicator 14a, 14b can independently be selected as a porous material configured to transport the liquid composition from the respective chamber 11a, 11b to a substrate in contact with the outer surface of the applicator 14a, 14b. The liquid composition can be brought into contact with the applicator 14a, 14b by bringing the dispensing applicator 14a, 14b into contact with a fixed-position surface (which can but does not have to be the substrate to be coated) and applying hand pressure on the housing 10a, 10b toward the surface to open the poppet valve 15a, 15b. The dispensing applicators 14a, 14b are slideably mounted in the housing 10a, 10b. At rest, the dispensing applicators 14a, 14b are biased away from the main body of the housing 10a, 10b by applicator biasing members (not shown) to an at-rest position as shown in FIG. 1. This biasing force is transmitted through actuator 16a, 16b to apply an expansive force on the spring member 18a, 18b, which intern acts on the poppet valve 15a, 15b to keep it engaged on the barrier 12a, 12b and closed. Upon the application of hand pressure urging housing 10a, 10b toward the surface, the counteracting force of the surface acting on the dispensing each applicator 14a, 14b compresses the spring member 18a, 18b until the fully compressed spring and actuator engage against the poppet valve 15a, 15b and displace it away from the barrier 12a, 12b to open the poppet valve 15a, 15b. Hand pressure can be maintained to keep the poppet valve open for a period of time sufficient to charge a desired quantity of liquid into chamber 17a, 17b, at which point the hand pressure can be removed or relaxed so that the applicator biasing members again bias the applicators 14a, 14b to the at-rest position with the poppet valve 15a, 15b closed. Liquid in the chamber 17a, 17b can then continue to be delivered and spread on the substrate. Of course, the applicators 14a, 14b are not limited to porous pads. The applicators 14a, 14b could also be independently selected from brushes, rollers, nozzles, etc. When not in use, the applicators 14a, 14b can be covered with an air- and liquid-tight cap.
  • Another example embodiment of a kit is schematically depicted in FIG. 2, in which the first and second containers are configured as first and second chambers 11a, 11b formed by housing 10 and barrier 20, with applicators 14a, 14b disposed at opposing ends of the oblong or cylindrical housing 10. The remaining components and features depicted in FIG. 2 and their operation are as in FIG. 1, and do not require further explanation. The embodiment depicted in FIG. 2 provides additional technical benefits of convenience and efficiency, while reducing the potential for cross-contamination between the compositions by delivering the two distinct chemical compositions through applicators disposed on opposite ends of a coating pen.
  • In some embodiments, avoidance of contamination from chromium salts on the substrate being coated into the second container comprising the oxidizing agent composition is promoted by contamination-avoiding materials or components. In some embodiments, the applicator 14b can be formed from a material that is resistant to wicking of material from the coated substrate into the chamber 17b from which it could potentially infiltrate to the chamber 11b when the poppet valve 15b is open. Such materials can include surfaces that are resistant to wetting by the coated chromium salt composition. In some embodiments, the poppet valve 15b can include check-valve features (not shown, but known in the valve art) to prevent migration of fluid from chamber 17b into chamber 11b. In some embodiments, anti-contamination procedures can be followed such as draining or flushing the chamber 17b after application is complete, or using a surface other than the coated substrate for displacing the applicator 14b to charge the chamber 17b so that the poppet valve 15b is closed before the applicator 14b comes into contact with the coated substrate. Combinations of the above materials or procedures can be used as well.
  • In some embodiments, the first liquid composition comprising the trivalent chromium salt can be allowed to contact the substrate for a period of time before applying the second composition comprising the oxidizing agent, and in some embodiments the kit can include instructions to that effect. The amount of contact time can vary considerably depending on the ambient temperature and humidity, the specific properties of the applicator and the liquid composition, and the thickness with which it is applied. Any amount of contact time greater than zero can be used. In some embodiments, contact times can range from 1 minute to 5 minutes. In some embodiments, contact times can range from 1 minute to 3 minutes.
  • In some embodiments, a wet layer of the second liquid composition comprising the oxidizing agent is maintained on the coated substrate for a minimum period of time. Although this disclosure is not bound by any theory of operation, it is believed that the wet layer promotes chemical interaction of the oxidizing agent with the trivalent chromium salt composition. Examples of minimum wet layer time limits can include 0.5 minutes, more specifically 1 minute, more specifically 1.5 minutes, more specifically 2 minutes, more specifically 3 minutes, more specifically 4 minutes, and even more specifically 5 minutes. Theoretically there is no maximum wet layer time; however, minimization of the opportunity costs of lost efficiency typically results in drying times that do not drastically exceed the specified minimum wet layer time. In some embodiments, a wet layer of the second liquid composition comprising the oxidizing agent is maintained by making a plurality of passes over the substrate with the applicator 14b, and in some embodiments the kit can include instructions to that effect. In some embodiments, the second liquid composition can be configured to maintain a wet layer for a target duration, e.g., through the inclusion of additives such as gel or thickening agents (e.g., fused silica, water soluble polymers) or lower volatility solvents. Moisture can also be retained by film-forming agents in the first composition such as sodium or potassium salts of hexafluorotitanic acid or hexafluorozirconic acid, or the selection of a chromium salt with colligative properties such as high solubility that render it inherently slow-drying.
  • While the present disclosure has been described in detail in connection with only a limited number of embodiments, it should be readily understood that the present disclosure is not limited to such disclosed embodiments. Rather, the present disclosure can be modified to incorporate any number of variations, alterations, substitutions or equivalent arrangements not heretofore described, but which are commensurate with the scope of the present invention as defined by the claims. Additionally, while various embodiments of the present disclosure have been described, it is to be understood that aspects of the present disclosure may include only some of the described embodiments. Accordingly, the present disclosure is not to be seen as limited by the foregoing description, but is only limited by the scope of the appended claims.

Claims (15)

  1. A kit for applying a conversion coating, comprising:
    a first handheld container (10a) comprising a first liquid composition disposed therein that comprises a trivalent chromium salt;
    a first applicator (14a) in fluid communication with the first container configured to dispense the first composition;
    a second handheld container (10b) comprising a second liquid composition disposed therein comprising an oxidizing agent; and
    a second applicator (14b) in fluid communication with the second container configured to dispense the second composition.
  2. The kit of claim 1, comprising a housing (10) that comprises a first chamber (11a) as said first container and a second chamber as said second container (11b).
  3. The kit of claim 1, comprising an oblong handheld housing that comprises a first chamber (11a) as said first container and a second chamber (11b) as said second container, the first applicator (14a) comprising a porous pad disposed at a first end of the oblong housing in fluid communication with the first chamber, and the second applicator (14b) comprising a porous pad disposed at a second end of the oblong housing in fluid communication with the second chamber.
  4. The kit of claim 1, comprising a first housing (10a) that comprises a first chamber (11a) as said first container, and a second housing (10b), separate from the first housing, that comprises a second chamber (11b) as the second container.
  5. The kit of claim 4, comprising a first oblong handheld housing that comprises a first chamber as said first container and the first applicator (14a) comprising a porous pad disposed at an end of the first oblong housing in fluid communication with the first chamber, and a second oblong housing that comprises a second chamber as said second container and the second applicator (14b) disposed at an end of the second oblong housing comprising a porous pad in fluid communication with the second chamber.
  6. The kit of any of claims 1-5, wherein the applicators are each independently selected from porous pads, brushes, rollers, or nozzles.
  7. The kit of any of claims 1-6, wherein the applicator in fluid communication with the second container is configured to make contact with a substrate to apply the second composition to the substrate, and wherein the second container and the applicator in fluid communication with it are configured to prevent fluid communication from the applicator to the second container.
  8. The kit of any of claims 1-7, wherein the oxidizing agent is selected from a peroxide, a permanganate salt, or combinations comprising the foregoing.
  9. The kit of claim 8, wherein the oxidizing agent comprises hydrogen peroxide.
  10. The kit of claim 9, wherein the second composition comprises 0.1 wt.% to 10 wt.% hydrogen peroxide, based on the total weight of the second composition.
  11. The kit of any of claims 1-10, wherein the second liquid composition is configured to stay wet on a substrate for at least 0.5 minutes.
  12. The kit of any of claims 1-11, further comprising instructions to apply a plurality of passes of the second composition to a substrate at intervals configured to maintain a wet layer of the second composition on the substrate for at least 0.5 minutes, or instructions to allow a drying period of time after application of the first composition to a substrate before applying the second composition, or both instructions to apply a plurality of passes of the second composition to a substrate at intervals configured to maintain a wet layer of the second composition on the substrate for at least 0.5 minutes and instructions to allow a drying period of time after application of the first composition to a substrate before applying the second composition.
  13. A method of using the kit of any of claims 1-12, comprising applying a coating of the first composition to a substrate, allowing a drying period of time to pass, applying the second composition to the coated substrate, and maintaining a wet layer of the second composition on the coated substrate for at least 0.5 minutes.
  14. A method of protecting a trivalent chromium conversion-coated substrate from corrosion, comprising contacting the substrate with a porous pad disposed on an end of an oblong handheld housing in fluid communication with a chamber disposed within the housing, and dispensing a liquid composition comprising an oxidizing agent disposed in the chamber onto the substrate through the porous pad, and maintaining a wet layer of the liquid composition on the substrate for at least 0.5 minutes.
  15. The method of claims 13 or 14, comprising applying a plurality of passes of the second composition or the liquid composition, respectively, to the substrate at intervals to maintain a wet layer on the substrate for at least 0.5 minutes, or optionally for at least 3 minutes or for at least 5 minutes.
EP17170451.3A 2016-05-10 2017-05-10 Conversion coating treatment Withdrawn EP3243928A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15/151,114 US20170327955A1 (en) 2016-05-10 2016-05-10 Conversion coating treatment

Publications (1)

Publication Number Publication Date
EP3243928A1 true EP3243928A1 (en) 2017-11-15

Family

ID=58709253

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17170451.3A Withdrawn EP3243928A1 (en) 2016-05-10 2017-05-10 Conversion coating treatment

Country Status (3)

Country Link
US (1) US20170327955A1 (en)
EP (1) EP3243928A1 (en)
JP (1) JP2017203215A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022531931A (en) * 2019-05-10 2022-07-12 ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング Applicator for harmful substances
US11951506B2 (en) 2022-09-08 2024-04-09 Hamilton Sundstrand Corporation Two part applicator pen

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5304257A (en) 1993-09-27 1994-04-19 The United States Of America As Represented By The Secretary Of The Navy Trivalent chromium conversion coatings for aluminum
US5374347A (en) 1993-09-27 1994-12-20 The United States Of America As Represented By The Secretary Of The Navy Trivalent chromium solutions for sealing anodized aluminum
WO1999026794A1 (en) * 1997-11-24 1999-06-03 Jacqueline Fulop Marking and eradicating instrument and method of use of same
US6048921A (en) * 1994-12-23 2000-04-11 Henkel Corporation Method for applying conversion coating with wick applicator
US6217935B1 (en) * 1991-11-22 2001-04-17 Henkel Corporation Method and hand held pen type applicator for applying hazardous chemicals
US6375726B1 (en) 2000-10-31 2002-04-23 The United States Of America As Represented By The Secretary Of The Navy Corrosion resistant coatings for aluminum and aluminum alloys
US6511532B2 (en) 2000-10-31 2003-01-28 The United States Of America As Represented By The Secretary Of The Navy Post-treatment for anodized aluminum
US6521029B1 (en) 2000-10-31 2003-02-18 The United States Of America As Represented By The Secretary Of The Navy Pretreatment for aluminum and aluminum alloys
DE102009039887A1 (en) * 2009-09-03 2011-03-17 Innovent E.V. Method for surface-treatment of magnesium-containing component, comprises applying a chemical passivating solution that consists of thixotropic agent, on a part of the surface and leaving the passivating solution on the surface

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6217935B1 (en) * 1991-11-22 2001-04-17 Henkel Corporation Method and hand held pen type applicator for applying hazardous chemicals
US5304257A (en) 1993-09-27 1994-04-19 The United States Of America As Represented By The Secretary Of The Navy Trivalent chromium conversion coatings for aluminum
US5374347A (en) 1993-09-27 1994-12-20 The United States Of America As Represented By The Secretary Of The Navy Trivalent chromium solutions for sealing anodized aluminum
US6048921A (en) * 1994-12-23 2000-04-11 Henkel Corporation Method for applying conversion coating with wick applicator
WO1999026794A1 (en) * 1997-11-24 1999-06-03 Jacqueline Fulop Marking and eradicating instrument and method of use of same
US6375726B1 (en) 2000-10-31 2002-04-23 The United States Of America As Represented By The Secretary Of The Navy Corrosion resistant coatings for aluminum and aluminum alloys
US6511532B2 (en) 2000-10-31 2003-01-28 The United States Of America As Represented By The Secretary Of The Navy Post-treatment for anodized aluminum
US6521029B1 (en) 2000-10-31 2003-02-18 The United States Of America As Represented By The Secretary Of The Navy Pretreatment for aluminum and aluminum alloys
DE102009039887A1 (en) * 2009-09-03 2011-03-17 Innovent E.V. Method for surface-treatment of magnesium-containing component, comprises applying a chemical passivating solution that consists of thixotropic agent, on a part of the surface and leaving the passivating solution on the surface

Also Published As

Publication number Publication date
US20170327955A1 (en) 2017-11-16
JP2017203215A (en) 2017-11-16

Similar Documents

Publication Publication Date Title
ES2730005T3 (en) Wet wet process and chrome-free acid solution for the corrosion protection treatment of steel surfaces
US11149353B2 (en) Anti-corrosion and/or passivation compositions for metal-containing substrates and methods for making, enhancing, and applying the same
KR102255735B1 (en) System and method for metal substrate treatment through thin film pretreatment and sealing composition
CA2312807A1 (en) Chromium-free corrosion protection agent and method for providing corrosion protection
US8728251B2 (en) Treatment solution for coating metal surface
EP3243928A1 (en) Conversion coating treatment
JPH02118081A (en) Pretreatment of metal surface
CN115595569A (en) Azole compounds as corrosion inhibitors
CN109112555A (en) Alkaline cleaning composition for metal base
CN109563629A (en) For handling the system and method for metal base
CN109642326A (en) Pretreatment compositions
CN102489435A (en) Coating process for vehicle wheel with finish-tuned and polished surface
US6027578A (en) Non-chrome conversion coating
JP2012097329A (en) Finishing agent for chemical film containing no hexavalent chromium
ES2905136T3 (en) Chromium (III)-containing treatment solution for a method for generating an anticorrosive coating layer, concentrate of said treatment solution and a method for generating an anticorrosive coating layer
US10415140B2 (en) Two-stage pre-treatment of aluminum comprising pickling and passivation
CN106232872B (en) The coloured conversion coatings of non-chromate for aluminium
WO2018006270A1 (en) Chromium-free aluminum conversion coating agent, aluminum material, and surface conversion coating treatment method
JP6594678B2 (en) Surface treatment agent, surface treatment method, and surface-treated metal material
KR100491122B1 (en) Method for manufacturing green chrome-free steel plate with a fingerprint-resistance
TWI531679B (en) Steel pre-paint treatment composition
Oki Performance of Tannin/Glycerol-Chromate hybrid conversion coating on aluminium
RU2510432C1 (en) Composition for removing rust and preserving surfaces of metal structures and pipes before painting
AU2003302934A1 (en) Aqueous coating solutions and method for the treatment of a metal surface
CN106047127A (en) Sealing agent for corrosion resistance of zinc-plated spring and preparation method thereof

Legal Events

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

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20180515

RBV Designated contracting states (corrected)

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20191021

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

STAA Information on the status of an ep patent application or granted ep patent

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

18D Application deemed to be withdrawn

Effective date: 20211008