BACKGROUND
[0001] This disclosure relates to coatings for corrosion protection, and more specifically
to conversion coatings for corrosion protection of metal substrates.
[0002] 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.
[0003] 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
[0004] 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.
[0005] 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.
[0006] 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
[0007] 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
[0008] 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.
[0009] 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 Cr
2(SO
4)
3, (NH)
4Cr(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. 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.
[0010] In some embodiments, the oxidizing agent can be a peroxide or a permanganate salt.
In some embodiments, the oxidizing agent is hydrogen peroxide (H
2O
2). Examples of peroxides other than hydrogen peroxide include inorganic peroxides
(e.g. Li
2O
2, Na
2O
2, K
2O
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.
[0011] 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.
[0012] 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.
[0013] 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.
[0014] 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.
[0015] 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.
[0016] 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.
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.