U.S. patent application number 10/934867 was filed with the patent office on 2005-02-03 for universal aqueous coating compositions for pretreating metal surfaces.
Invention is credited to Beck, Leslie M., Claffey, William J., McIntyre, John F..
Application Number | 20050022907 10/934867 |
Document ID | / |
Family ID | 29582076 |
Filed Date | 2005-02-03 |
United States Patent
Application |
20050022907 |
Kind Code |
A1 |
Claffey, William J. ; et
al. |
February 3, 2005 |
Universal aqueous coating compositions for pretreating metal
surfaces
Abstract
A universal aqueous composition and a process for using such a
composition for pretreating metal substrates is provided. The
aqueous composition includes a hydroxy functional cyclic compound,
such as a tannin, in an amount of at least about 500 ppm, phosphate
ions, an oxidizer-accelerator, and at least one Group IVB metal
compound capable of converting to a metal oxide upon application to
the metal substrate, such as a fluorozirconate or fluorotitanate.
The composition may further contain fluoride ions and/or iron The
composition is particularly useful for corrosion resistance with a
variety of metals such as iron, steel; zinc-coated surfaces,
aluminum, and alloys thereof. A disaccharide may further be
provided to prolong the useful life of the composition,
particularly when used in spray applications.
Inventors: |
Claffey, William J.;
(Novelty, OH) ; McIntyre, John F.; (Bay Village,
OH) ; Beck, Leslie M.; (Concord, OH) |
Correspondence
Address: |
PPG INDUSTRIES, INC.
Intellectual Property Department
One PPG Place
Pittsburgh
PA
15727
US
|
Family ID: |
29582076 |
Appl. No.: |
10/934867 |
Filed: |
September 3, 2004 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10934867 |
Sep 3, 2004 |
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10153022 |
May 22, 2002 |
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6805756 |
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Current U.S.
Class: |
148/247 |
Current CPC
Class: |
C23C 22/10 20130101;
C23C 2222/20 20130101; C23C 22/361 20130101 |
Class at
Publication: |
148/247 |
International
Class: |
C23C 022/48 |
Claims
1. An aqueous composition for pretreating metal substrates
comprising: a) at least one hydroxy functional cyclic compound
present in an amount of at least about 500 ppm, said hydroxy
functional cyclic compound selected from the group consisting of
polyhydroxy phenolic compounds and heterocyclic nitrogen-containing
compounds having hydroxy functionality; b) phosphate ions; c) at
least one oxidizer-accelerator selected from alkali metal chlorate,
alkali metal bromate, alkali metal perchlorate, alkali metal
chlorite, alkali metal nitrite, alkali metal perborate, ammonium
chlorate, ammonium bromate, ammonium perchlorate, ammonium
chlorite, ammonium nitrite, ammonium perborate, hydrogen peroxide,
nitroguanidine, halo- or nitro-substituted benzene sulfonic acids,
alkali metal salts of halo- or nitro-substituted benzene sulfonic
acids, ammonium salts of halo- or nitro-substituted benzene
sulfonic acids, and mixtures thereof; d) at least one Group IVB
metal compound capable of converting to a metal oxide upon
application to the metal substrate; and e) water.
2. The composition of claim 1 wherein the hydroxy functional cyclic
compound is selected from the group consisting of catechol,
methylene-bridged poly(alkylphenols), coumaryl alcohol, coniferyl
alcohol, hydroxyalkyl celluloses, lignin, tannin, sinapyl alcohol,
and mixtures thereof.
3. The composition of claim 1 wherein the hydroxy functional cyclic
compound is at least one tannin material.
4. The composition of claim 3 wherein the tannin material is
selected from the group consisting of vegetable tannin,
hydrolyzable tannin, condensable tannin, tannic acid, and mixtures
thereof.
5. The composition of claim 4 wherein the tannin material is at
least one of quebracho and mimosa tannins.
6. The composition of claim 1 wherein said hydroxy functional
cyclic compound is present in an amount of about 500 ppm to about
2,500 ppm.
7. The composition of claim 1 wherein said phosphate ions are
present in an amount of about 125 to about 300 ppm.
8. The composition of claim 1 wherein said oxidizer accelerator is
present in an amount of about 10 to about 10,000 ppm.
9. The composition of claim 1 wherein said Group IVB metal compound
is present in an amount of about 60 to about 600 ppm.
10. The composition of claim 1, having a pH within the range of
about 3.5 to about 5.
11. The composition of claim 1 wherein said Group IVB metal
compound is selected from the group consisting of
hexafluorozirconic acid and hexafluorotitanic acid and their
soluble salts.
12-13. (cancelled)
14. The composition of claim 1, wherein said oxidizer-accelerator
comprises a mixture of an alkali metal salt of meta-nitrobenzene
sulfonic acid and at least one alkali metal chlorate.
15. The composition of claim 1, further comprising at least one
disaccharide.
16. The composition of claim 15, wherein the disaccharide is
selected from the group consisting of lactose and sucrose.
17. The composition of claim 11 wherein the disaccharide is present
in an amount of 500 to 10,000 ppm.
18. A process for pretreating a metal substrate comprising
contacting the substrate with an aqueous composition which
comprises: a) at least one hydroxy functional cyclic compound
present in an amount of at least about 500 ppm, said hydroxy
functional cyclic compound selected from the group consisting of
hydroxy phenolic compounds and heterocyclic nitrogen-containing
compounds having hydroxy functionality; b) phosphate ions; c) at
least one oxidizer-accelerator selected from alkali metal chlorate,
alkali metal bromate, alkali metal perchlorate, alkali metal
chlorite, alkali metal nitrite, alkali metal perborate, ammonium
chlorate, ammonium bromate, ammonium perchlorate, ammonium
chlorite, ammonium nitrite, ammonium perborate, hydrogen peroxide,
nitroguanidine, halo- or nitro-substituted benzene sulfonic acids,
alkali metal salts of halo- or nitro-substituted benzene sulfonic
acids, ammonium salts of halo- or nitro-substituted benzene
sulfonic acids, and mixtures thereof; d) at least one Group IVB
metal compound capable of converting to a metal oxide upon
application to the metal substrate; and e) water.
19. The process of claim 18 wherein the metal substrate is selected
from the group consisting of cold rolled steel, steel
surface-treated with any of zinc metal, zinc compounds and zinc
alloys; aluminum; aluminum alloys; zinc-aluminum alloys; aluminum
plated steel; and aluminum alloy plated steel.
20. The process of claim 18 wherein the metal substrate is a
combination of two or more metal substrates assembled together.
21. The process of claim 18 wherein the metal substrate is
contacted with the aqueous composition by immersion.
22. The process of claim 18 wherein the metal substrate is
contacted with the aqueous composition by spray application.
23. The process of claim 18 wherein the aqueous composition further
comprises at least one disaccharide selected from the group
consisting of lactose and sucrose.
24. The process of claim 18 wherein the aqueous composition is at
ambient temperature.
25. The process of claim 18 further comprising the step of rinsing
the metal substrate with an aqueous solution containing silane
after contact with the aqueous composition.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to coating compositions for
pretreating metal surfaces. More particularly, the present
invention is directed to aqueous coating compositions for providing
durable, adhesive and corrosion-inhibiting coatings, as well as a
method for pretreating metal substrates with such coating
compositions.
BACKGROUND OF THE INVENTION
[0002] Pretreatment of metal surfaces such as aluminum, ferrous and
zinc surfaces with inorganic phosphate compositions and/or coatings
by contacting such surfaces with an aqueous phosphating solution is
well known. Such phosphate pretreatment processes protect the metal
surface to a limited extent against corrosion, and serve as an
effective base for the later application of organic coating
compositions such as paint, lacquer, varnish, primer, synthetic
resin, enamel, and the like.
[0003] Inorganic phosphate coatings generally are formed on a metal
surface by means of an aqueous solution which contains phosphate
ion and, optionally, certain auxiliary ions including metallic ions
such as iron, sodium, manganese, zinc, cadmium, copper, lead,
calcium-zinc, cobalt, nickel and antimony ions. These aqueous
solutions also may contain non-metallic ions-such as halide ions,
nitrate ions, sulfate ions and borate ions. Recent advances in the
pretreatment field have been directed to coatings derived from
solutions containing a minimum of three metal cations such as zinc,
cobalt, nickel, manganese, magnesium or calcium.
[0004] Chromium-free compositions have been proposed as rinse
compositions for improving the quality of coated metal substrates.
For example, U.S. Pat. No. 3,695,942 discloses a zirconium rinse
for use with metal surfaces which have been pretreated with a
phosphate conversion coating.
[0005] Aqueous pretreatment processes with coating compositions
including an organic compound such as tannin, phosphate ions and an
oxidizing agent are taught through U.S. Pat. No. 5,868,820. Such
pretreatment processes and compositions typically require immersion
or deposition of the coating composition at temperatures of
120.degree. F. Chromium-free compositions and-titanium and
zirconium compositions are disclosed as rinse compositions for
application over the first coating composition. Such pretreatment
processes and compositions involve multiple coatings in order to
provide satisfactory results over a variety of different metal
substrates.
[0006] U.S. Pat. No. 4,338,140 discloses coating compositions for
improving corrosion resistance over metal surfaces such as aluminum
cans, which includes dissolved hafnium and/or zirconium, fluoride,
up to about 500 parts per million of a vegetable tannin compound,
and optionally, phosphate ions.
[0007] While prior art pretreatment processes can be effective,
they typically require processing conditions involving elevated
temperatures, and are typically useful for only selected metal
substrates.
[0008] Accordingly, there is a need for a pretreatment process
which can be conducted at ambient conditions and which can provide
effective properties for a variety of substrate materials.
SUMMARY OF THE INVENTION
[0009] The present invention includes an aqueous composition for
pretreating metal substrates. The aqueous composition includes at
least one hydroxy functional cyclic compound present in an amount
of at least about 500 ppm, with the hydroxy functional cyclic
compound being selected from the group consisting of hydroxy
phenolic compounds and heterocyclic nitrogen-containing compounds
having polyhydroxy functionality, such as a tannin, for example
quebracho and/or mimosa tannins. The aqueous composition further
includes phosphate ions, at least one oxidizer-accelerator, at
least one Group IVB metal compound capable of converting to a metal
oxide upon application to the metal substrate, and water. The Group
IVB metal compound is preferably selected from the group consisting
of hexafluordzirconic acid and hexafluorotitanic acid and their
soluble salts.
[0010] The composition of the present invention may further include
at least one disaccharide, such as those selected from the group
consisting of lactose and sucrose.
[0011] The present invention further relates to a process for
pretreating a metal substrate. The process includes contacting the
substrate with an aqueous composition which includes at least one
hydroxy functional cyclic compound present in an amount of at least
about 500 ppm; phosphate ions; at least one oxidizer-accelerator;
at least one Group IVB metal compound capable of converting to a
metal oxide upon application to the metal substrate; and water. The
process is particularly useful for improving corrosion resistance
of a variety of substrates, including cold rolled steel, steel
surfaces treated with any of zinc metal, zinc compounds and zinc
alloys; aluminum; aluminum alloys; zinc-aluminum alloys; aluminum
plated steel; and aluminum alloy plated steel. The process includes
contacting the metal substrate with the aqueous composition, for
example by immersion or by spray application. The process may
further include a rinsing step, such as by rinsing the metal
substrate with an aqueous solution containing silane or an epoxy
derivative after contact with-the aqueous composition.
DETAILED DESCRIPTION OF THE INVENTION
[0012] Other than in the operating examples, or where otherwise
indicated, all numbers expressing quantities of ingredients,
reaction conditions and so forth used in the specification and
claims are to be understood as being modified in all instances by
the term "about." Accordingly, unless indicated to the contrary,
the numerical-parameters set forth in the following specification
and attached claims are approximations that may vary depending upon
the desired properties sought to be obtained by the present
invention. At the very least, and not as an attempt to limit the
application of the doctrine of equivalents to the scope of the
claims, each numerical parameter should at least be construed in
light of the number of reported significant digits and by applying
ordinary rounding techniques.
[0013] Notwithstanding that the numerical ranges and parameters
setting forth the broad scope of the invention are, approximations,
the numerical values set forth in the specific examples are
reported as precisely as possible. Any numerical values, however,
inherently contain certain errors necessarily resulting from the
standard deviation found in their respective testing
measurements.
[0014] Also, it should be understood that any numerical range
recited herein is intended to include all sub-ranges subsumed
therein. For example, a range of "1 to 10" is intended to include
all sub-ranges between (and including) the recited minimum value of
1 and the recited maximum value of 10, that is, having a minimum
value equal to or greater than 1 and a maximum value of equal to or
less than 10.
[0015] As indicated, the present invention is directed to aqueous
compositions for pretreating metal substrates. The compositions of
the present invention may be utilized to improve the
corrosion-inhibiting properties of metal surfaces such as iron,
steel, and zinc-coated surfaces. The coatings deposited by the
compositions of the present invention can be used to replace
non-reactive inorganic metal treatments such as iron phosphate,
zinc phosphate and chromium conversion coatings.
[0016] In one embodiment of the invention, the aqueous coating
composition includes at least one polyhydroxy functional cyclic
compound selected from the group consisting of polyhydroxy phenolic
compounds and heterocyclic nitrogen-containing compounds having
polyhydroxy functionality, phosphate ions, and an
oxidizer-accelerator. In addition, the coating composition includes
at least one Group IVB metal compound capable of converting to a
metal oxide upon application to the metal substrate.
[0017] The cyclic hydroxy compound is selected from cyclic
polyhydroxy compounds and substituted phenols. A variety of cyclic
hydroxy compounds can be utilized in the present invention and
these include phenolic compounds such as catechol,
methylene-bridged poly(alkylphenols), coumaryl alcohol, coniferyl
alcohol, sinapyl alcohol, lignin and tannic acid, or non-phenolic
compounds such as ascorbic acid, hydroxy alkyl celluloses such as
hydroxy methyl cellulose, hydroxy ethyl cellulose and hydroxy
propyl cellulose, and heterocyclic nitrogen-containing compounds
also containing polyhydroxy functionality such as
glycolurilformaldehyde amino resin having the general structure
1
[0018] In the cyclic hydroxy compounds, at least one hydroxy group
is attached directly to a ring and another hydroxy group may be on
an aliphatic group.(e.g., --CH.sub.2OH) attached to the ring.
[0019] Tannin or tannic acid is a polyphenolic substance which is a
preferred example of the cyclic polyhydroxy compounds which are
useful in the aqueous coating compositions of the present
invention. Tannins are polyphenolic compounds which are extracted
from various plants and trees, which can be classified according to
their chemical properties as (a) hydrolyzable tannins; (b)
condensed tannins; and (c) mixed tannins containing both
hydrolyzable and condensed tannins. Preferred tannin materials
useful in the present invention are those that contain a tannin
extract from naturally occurring plants and trees, and are normally
referred to as vegetable tannins. Suitable vegetable tannins
include the crude, ordinary or hot-water-soluble condensed,
vegetable tannins. Quebracho and mimosa are preferred condensed
vegetable tannins. Other vegetable tannins include mangrove,
spruce, hemlock, gabien, wattles, catechu, uranday, tea, larch,
myrobalan, chestnut wood, divi-divi, valonia, summac, chinchona,
oak, etc. These vegetable tannins are not pure chemical compounds
with known structures, but rather contain numerous components
including phenolic moieties such as catechol, pyrogallol, etc.,
condensed into a complicated polymeric structure.
[0020] The cyclic hydroxy-compounds utilized in the coating
compositions of the present invention also may be substituted
phenolic compounds containing only one hydroxyl group. The
substituents on the phenolic compounds may be alkyl, hydroxyalkyl,
or alkoxy groups containing from 1 to about. 6 or more carbon
atoms. Specific examples of alkyl groups include methyl, ethyl,
propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, amyl, etc.
Examples of alkoxy groups include methoxy, ethoxy, propoxy, etc. In
one preferred embodiment, the phenolic compounds will be
substituted with two or more alkyl or alkoxy groups. Examples of
substituted phenols useful in the coating compositions of the
present invention include 4-hydroxybenzyl alcohol,
2,6-dimethylphenol, 2,6-di-tert-butylphenol,
2,6-di-t-butyl-p-cresol, etc.
[0021] The aqueous compositions of the present invention preferably
contains at least about 500 ppm of the cyclic polyhydroxy compound
described above. More preferably, the aqueous compositions of the
present invention contains from about 500 ppm to about 2,500 ppm of
the cyclic polyhydroxy compound, and in particularly desirable
applications, about 1,500 ppm of the cyclic polyhydroxy compound.
Incorporating the cyclic polyhydroxy compound, and in particular
tannin, at such high levels, provides the coating composition with
excellent adhesion to a variety of substrate materials, including
steel, zinc-coated steel and aluminum.
[0022] In an alternate embodiment of the invention, the cyclic
polyhydroxy compound is reacted with a further organic compound. As
such, derivative compounds, such as derivatives of native tannins,
can be prepared and used in the compositions of the present
invention. For example, phenyl glycidyl ether can be reacted with
mimosa tannin with a ratio of one mole of tannin hydroxy groups to
a half mole of epoxy.
[0023] The aqueous coating composition of the present invention
also contains phosphate ions. In one particular embodiment, the
coating composition contains from about 10 to about 500 ppm of
phosphate ions, more preferably from about 125 to 300 ppm. The
source of the phosphate ions in the aqueous coating composition of
the present invention is typically phosphoric acid such as 75%
phosphoric acid, although other sources are contemplated by the
present invention.
[0024] An alkali metal hydroxide such as sodium hydroxide or
potassium hydroxide may be added to the aqueous coating composition
of the present invention in an amount sufficient to convert the
phosphoric acid to an alkali metal phosphate such as sodium
phosphate or potassium phosphate. Additionally, an amine hydroxide
(ammonium hydroxide) may be added to convert phosphoric acid to
ammonium phosphate. Other phosphate sources include sodium acid
pyrophosphate, potassium acid pyrophosphate, polyphosphates and
combinations thereof.
[0025] The aqueous coating compositions also contain at least one
oxidizer-accelerator which increases the rate of deposition of the
coating. The oxidizer-accelerators useful in the present invention
may be inorganic or organic accelerators. Examples of inorganic
oxidizer-accelerators include alkali metal and ammonium chlorates,
bromates, perchlorates, chlorites, nitrates, nitrites, molybdates,
perborates, or mixtures thereof. Dilute solutions of hydrogen
peroxide also are effective as oxidizers-accelerators in the
coating compositions. Alternatively, high volume air sparging of
the coating composition, is effective as an oxidizer-accelerator
when the composition is in contact with the metal surface. Examples
of organic oxidizer-accelerators include nitroguanidine, halo- or
nitro-substituted benzene sulfonic acids and the alkali metal and
ammonium salts of said sulfonic acids. Alkali metal salts of
nitro-substituted benzene. sulfonic acids, and more particularly,
metanitrobenzene sulfonic acid are particularly useful
oxidizer-accelerators, particularly in combination with one or more
of the inorganic accelerators such as the alkali metal chlorates
and nitrates. Thus, a particularly useful oxidizer-accelerator
comprises the mixture of at least one alkali metal chlorate or
nitrate and sodium meta-nitrobenzene sulfonate. The amount of
oxidizer-accelerator included in the coating compositions may vary
over a wide range. Generally, the coating compositions will contain
from about 0.01 to about 3% by weight based on the total weight of
the composition of at least one oxidizer-accelerator, although
amounts of up to about 1.5% by weight provide satisfactory
results.
[0026] The composition of the present invention further comprises
at least one metal compound which is capable of converting to a
metal oxide upon application to the metal substrate. The metal
compound which is the precursor of the formation of the metal oxide
on the surface of the substrate can be any metal compound capable
of converting to a metal oxide. The metal compound is preferably
selected from the Group IVB metals, most preferably zirconium or
titanium. Incorporation of the metal compound with the cyclic
compound, the phosphate ions and the oxidizer-accelerator in the
pretreatment composition provides a synergistic effect, which
improves adhesion of subsequently applied top coats, and permits
treatment at ambient temperature. While not wishing to be bound by
any particular theory, it is believed that the pretreatment
composition allows for co-deposition of a metal oxide from the
metal compound, as well as the cyclic compound and phosphate ions.
Such co-deposition provides a synergistic effect for pretreatment
of metal substrates.
[0027] As indicated, the metal compound is selected from the Group
IVB transition metals of the Periodic Table of the Elements, such
as those selected from the group consisting of titanium, zirconium
and hafnium ions and mixtures thereof. The Group IVB metal, and in
particular zirconium, is provided in ionic form, which is easily
dissolved in the aqueous composition. The metal ions may be
provided by the addition of specific compounds of the metals, such
as their soluble acids and salts, including, for example, nitrate,
sulfate, fluoride, acetate, citrate and/or chloride salts, and
mixtures and combinations thereof. Soluble alkali metal salts are
particularly desirable. Examples of useful compositions include
fluorozirconic acid, fluorotitanic acid, ammonium and alkali metal
fluorozirconates and fluorotitanates, zirconium fluoride, zirconium
nitrate, zirconium sulfate, and the like. Hexafluorozirconic acid
and hexafluorotitanic acid and their soluble salts are particularly
preferred. Examples of other particularly useful compounds include
fluorotitanates and fluorozirconates having coordination numbers
from 4 to 7, such as heptafluorozirconate, hexafluorozirconate,
pentafluorozirconate, and tetrafluorozirconate.
[0028] The metal compound is preferably present in the solution of
the present invention in an amount of from about 60 ppm to about
350 ppm.
[0029] As indicated, the coating compositions of the present
invention are provided as an aqueous solution. The balance of the
composition, therefore comprises water.
[0030] In addition, the aqueous coating compositions of the present
invention may also contain ferrous or ferric ions in amounts of up
to about 250 to 2,000 ppm. When the aqueous coating compositions of
the present invention are to be utilized to coat non-ferrous
surfaces such as zinc-coated surfaces, ferrous or ferric ions are
added to the coating composition. Water-soluble forms of iron can
be utilized as a source of the ferrous or ferric ions, and such
compounds include ferrous phosphate, ferrous nitrate, ferrous
sulfate, etc. When the surface to be coated is an iron surface, it
may not be necessary to add any or as much ferrous or ferric ions
since a portion of the iron surface is dissolved into the coating
composition upon contact.
[0031] In a further embodiment, the coating compositions of the
present invention will preferably contain fluoride ion in amounts
of up to about 0.3% by weight. Fluoride ion concentrations in the
range of from about 0.01 to about 1% by weight, and more often from
about 0.03 to about 0.3% by weight can be included in the aqueous
coating compositions of the invention. Water-soluble fluoride
compounds can be utilized to introduce the fluoride ion into the
coating compositions. Suitable fluoride compounds include alkali
metal fluorides such as sodium fluoride, ammonium fluoride salts
such as ammonium fluoride and ammonium bifluoride, other inorganic
fluoride salts such as sodium silicofluoride, ammonium
silicofluoride, hydrofluoric acid, hydrofluorosilicic acid and
fluoroboric acid. In preferred embodiments, the fluoride ions are
introduced into the composition through the Group IVB metal
compound, for example, through the use of an alkali metal
fluorozirconate compound.
[0032] The aqueous coating compositions of the present invention
generally are utilized at a pH of between about 3.5 to 5.0 and more
often, at a pH range of from about 4 to about 4.5. The pH of the
solution can be adjusted by the addition of an alkali such as
sodium hydroxide, potassium hydroxide or sodium carbonate to
increase the pH, or an acid such as phosphoric acid to reduce the
pH of the composition.
[0033] The coating compositions of the present invention can be
applied to substrate surfaces in any known manner, for example, by
immersion, dip coating, roll coating, spraying, and the like.
[0034] Moreover, it has been recognized through the present
invention that pretreatment of metal substrates with compositions
including metal ions do not provide consistent results. For
example, treatment of-steel substrates with coating compositions
including fluorozirconate by spray application of the coating
composition demonstrates a reduction in performance of the coating
composition as the bath containing the coating composition ages.
Similar reductions in performance are not seen, however, when the
steel substrate is coated with the same coating compositions by
immersion coating. Without wishing to be bound by any particular
theory, it is believed that the bath containing the coating
compositions for spray application continuously takes up oxygen
from the ambient air. Such oxygen promotes oxidation of the steel
substrate from the ferrous state to the ferric state. The zirconium
dioxide does not deposit on the steel in the ferric state, but only
on steel in the ferrous, state. Accordingly, it is proposed through
the present invention that improved universal coating compositions,
and in particular compositions useful for spray application to
steel substrates, can be achieved by further addition of a reducing
agent in the form of a disaccharide to the coating composition. It
has been discovered through the present invention that the use of
such a disaccharide maintains the iron in the ferrous state.
[0035] Examples of useful disaccharides include lactose, sucrose,
and mixtures thereof. The disaccharide is preferably present in the
coating composition in an amount of 50 to 10,000 ppm.
[0036] The aqueous coating compositions of the present invention
may be prepared by blending the various components described above
in water. In a preferred embodiment, the coating compositions are
prepared from a two-part system, wherein each part is separately
prepared and subsequently blended into additional water. Generally,
the mixture of the first part will contain water, the complex
fluoride of a Group IVB metal, phosphoric acid, sodium hydroxide,
one or more oxidizer-accelerators, and optionally, ammonium
bifluoride. The second part or mixture comprises water, an
oxidizer-accelerator, and the cyclic hydroxy compound(s). The two
parts are then blended into water at desired concentrations, and
the pH is adjusted with either sodium hydroxide or phosphoric acid
to the desired pH of from 3.5 to 5.0.
[0037] In yet another embodiment, the metal surfaces which have
been provided with a first coating in accordance with the present
invention, may be subsequently contacted with a silane.
[0038] In one embodiment, the silane compounds are characterized by
the formula
A.sub.(4-x)Si(B).sub.x (I)
[0039] wherein A is a hydrolyzable group, x is 1, 2 or 3, and B is
a monovalent organic group. The A groups are groups which hydrolyze
in the presence of water and may include acetoxy groups, alkoxy
groups containing up to 20 carbon atoms and chloro groups. In one
preferred embodiment, x=1 and each A is an RO group such as
represented by the formula
(RO).sub.3SiB (II)
[0040] wherein each R is independently an alkyl, aryl, aralkyl or
cycloalkyl group containing less than 20 carbon atoms, more often
up to about 5 carbon atoms. The number of hydrolyzable groups A
present in the silane coupling agent of Formula II may be 1, 2 or 3
and is preferably 3 (i.e., x=1). Specific examples of RO groups
include methoxy, ethoxy, propoxy, methylmethoxy, ethylmethoxy,
phenoxy, etc.
[0041] The Group B in Formula I may be an alkyl or aryl group, or a
functional group represented by the formula
C.sub.nH.sub.2nxX (III)
[0042] wherein n is from 0 to 20 and X is selected from the group
consisting of amino, amido, hydroxy, alkoxy, halo, mercapto,
carboxy, acyl, vinyl, allyl, styryl, epoxy, isocyanato, glycidoxy
and acryloxy groups. The alkyl and aryl groups may contain up to
about 10 carbon atoms. Alkyl groups containing from 1 to about 5
carbon atoms are particularly useful. In one embodiment, n is an
integer from 0 to 10 and more often from 1 to about 5.
[0043] The amino groups may contain one or more nitrogen atoms and,
thus, may be monoamino groups, diamino groups, triamino groups,
etc. General examples of diamino silanes can be represented by the
formula
A.sub.3SiR.sup.4N(R.sup.5)R.sup.4N(R.sup.5).sub.2 (IV)
[0044] wherein A is as defined in Formula I, each R.sup.4 is
independently a divalent hydrocarbyl group containing from 1 to
about 5 carbon atoms, and each R.sup.5 is independently hydrogen or
an alkyl or an aryl group containing up to about 10 carbon atoms.
The divalent hydrocarbyl groups include methylene, ethylene,
propylene, etc. Each R.sup.5 is preferably hydrogen or a methyl or
ethyl group.
[0045] The silanes which may contain amido groups include
compositions represented by Formula I wherein the Group B may be
represented by the formulae
--R.sup.4C(O)N(R.sup.5).sub.2 (V)
and
--R.sup.4-N(R.sup.5)C(O)N(R.sup.5).sub.2 (VI)
[0046] wherein each R.sup.4 is independently a divalent hydrocarbyl
group containing from 1 to 20 carbon atoms, more often from 1 to
about 5 carbon atoms, and each R.sup.5 is independently hydrogen or
an alkyl or aryl group containing up to about 10 carbon atoms.
Thus, the amido group may be an amide group or an ureido group.
Generally, each R.sup.5 in the formulae for the amido groups is
hydrogen or an alkyl group containing from 1 to about 5 carbon
atoms.
[0047] Examples of silanes useful in the present invention include
N-(2-aminoethyl)-3-aminopropyltrimethoxysilane,
3-methacryloxypropyltrime- thoxy-silane,
3-glycidoxypropyltrimethoxysilane, triacetoxyvinylsilane,
tris(2-methoxyethoxy)-vinylsilane, 3-chloropropyltrimethoxysilane,
3-chloropropyltriethoxysilane,
N-(aminoethylaminomethyl)phenyltrimethoxys- ilane,
N-(2-aminoethyl)-3-aminopropyl tris(2-ethylhexoxy)silane,
3-aminopropyltrimethoxysilane, trimethoxysilylpropylenetriamine,
.beta.-(3,4-epoxycyclohexyl)ethyltrimethoxysilane,
3-mercaptopropyltrimethoxy silane, 3-mercaptotriethoxysilane,
3-mercaptopropylmethyidimethoxysilane, bis
(2-hydroxyethyl)-3-amninopropy- ltrimethoxysilane,
1,3-divinyltetramethyidisilazane, vinyltrimethoxysilane,
3-isocyanatopropyidimethylethoxysilane,
N-(3-acryloxy-2-hydroxypropyl)-3-aminopropyltriethoxysilane,
methyltrimethoxysilane, ethyltrimethoxysilane,
phenyltrimethoxysilane, phenyltriacetoxysilane,
methyltrimethoxysilane, phenyltrimethoxysilane.
[0048] A number of organofunctional silanes are available, for
example, from Union Carbide, Specialty Chemicals Division, Danbury,
Conn. Examples of useful silanes available from Union Carbide are
disclosed in U.S. Pat. No. 5,868,820, the disclosure of which is
hereby incorporated herein by reference.
[0049] The silane may be applied to the coated metal surface as an
aqueous mixture. The concentration of the silane in the mixture may
range from about 0.01 to about 2% by weight. In one embodiment
where the silane is to be applied and dried without a water rinse,
a concentration of about 0.05 to about 0.15 is sufficient. If the
silane treated panel is to be subsequently rinsed with water,
silane concentrations of about 0.37 to about 1% or more are
used.
[0050] The present invention will now be described in terms of a
method of treating a metal substrate with the reactive organic
conversion coating composition as described above. Prior to
application of the coating composition, the surface of the metal
substrate is cleaned to remove contaminants such as dirt, grease,
oil or other residue therefrom. Such cleaning is well known in the
art, and may typically involve cleaning with a detergent,
preferably a water-based detergent, such as mild or strong alkaline
cleaners. Examples of suitable alkaline cleaners include BASE Phase
No-Phos or BASE Phase #6, both of which are available from PPG
Industries, Pretreatment and Specialty Products. Such cleaning is
generally followed and/or preceded by a water rinse.
[0051] Following cleaning and rinsing of the metal substrate, the
thus-cleaned surface is then coated with the reactive organic
conversion coating composition of the present invention. This
coating can be applied through any known technique, as described
above. Preferably, the coating is applied by spray coating. The
coating temperature is ambient, which may range from 15 to 30
degrees centigrade. Contact times of from about 5 seconds to about
5 minutes provide satisfactory coatings.
[0052] The concentration of the coating composition and the contact
time should be sufficient to provide a coating thickness or weight
which is sufficient to provide the desired corrosion resistance and
adhesion of subsequently applied coatings. Generally thin coatings
of about 50to about 300 nanometers thickness and coating weights of
from about 30 to about 60 mg/ft.sup.2 are employed. The coatings
deposited by the coating compositions of the present invention have
a pleasing optical appearance.
[0053] Following application of the conversion coating, the coating
is dried, arid preferably rinsed, optionally, with water. As with
the application of the coating composition, various contacting
techniques may be used for rinsing, such as dipping, spraying and
the like. Additionally, deionized water may be used as a final
rinse for the coating.
[0054] In specific embodiments employing an additional rinse or a
silane rinse, such rinse is provided between the water rinse and
the final deionized water rinse.
[0055] In addition, the metal surface containing the coating
composition as such may be contacted with an organic polymer resin
to form a second organic coating. Examples of organic polymers
which may be deposed over the first coating include
ureaformaldehyde resins, polyethyleneamine, polyethanolamine,
melamine-formaldehyde resins, epoxy based resins, etc.
[0056] The metal surfaces which have been provided with a first
coating of the aqueous coating compositions of the present
invention and, optionally, subsequently contacted with additional
coating compositions to form a second coating over the first
coating or, optionally, a seal coat, exhibit improved corrosion
resistance and improved adhesion to siccative organic coatings.
Siccative organic coatings which can be applied over the first or
second coatings as top-coats include paints, enamels, varnishes,
lacquers, synthetic resins, primers, etc. Such top-coats can be
applied by conventional means such as by spraying, brushing,
dipping, roller coating, or electrophoresis. After application of
the siccative top-coat, the treated metal surface is dried either
by exposure to the air or by means of a baking technique, depending
on the nature of the siccative top-coat material.
[0057] The siccative organic coating compositions may be organic
solvent based compositions. The organic solvents generally employed
in the protective coating industry include benzene, toluene,
xylene, mesitylene, ethylene dichloride, trichloroethylene;
diisopropyl ether, aromatic petroleum spirits, turpentine,
dipentene, amyl acetate, methyl isobutyl ketone, etc.
[0058] The siccative organic coating composition may also be a
water based or emulsion paint such as synthetic latex paints
derived from acrylic resins, polyvinyl alcohol resins, alkyd
resins, melamine resins, epoxy resins, phenolic resins, etc., by
emulsification thereof with water, as well as water-soluble paints
derived from water-soluble alkyd resins, acrylic resins, and the
like. The siccative organic coating may be a powder paint.
[0059] The siccative organic coating compositions may also contain
conventional improving agents such as pigment extenders,
anti-skinning agents, driers, gloss agents, color stabilizers,
etc.
[0060] The siccative organic coating composition may be applied to
the coated surface by techniques well known in the art for applying
siccative organic coatings such as paints. For example, the coating
may be applied by dipping, brushing, spraying, roller-coating,
flow-coating, and by the electrophoretic process of painting metal
surfaces. Often, the electrophoretic process is preferred because
of the improved results which are obtained.
[0061] The following examples demonstrate the preparation of
coating compositions of the present invention, as well as
comparisons of such coatings with prior art compositions. Unless
otherwise indicated in the examples and elsewhere in the
specification and claims, all parts and percentages are by weight,
temperatures are in degrees Centigrade, and pressures are at or
near atmospheric pressure.
EXAMPLES
Example 1
[0062] This is a comparative example, relating to a coating
composition prepared according to the teachings of Example 1 of
U.S. Pat. No. 5,868,820. The reactive organic conversion coating
bath contained per liter 18 grams of phosphoric acid, 4 g NaOH, 7 g
NaClO3, 0.7 g ammonium bifluoride, and 3 g of mixed tannins (equal
parts of quebracho and mimosa tannic acids), resulting in the
following concentrations:
1 COMPONENT CONCENTRATION, ppm Phosphoric Acid 18,000 NaOH 4,000
NaClO.sub.3 700 Ammonium Bifluoride 7,000 Tannin 3,000
[0063] The conversion composition was applied by spray for 60
seconds to individual panels of cold rolled steel (CRS),
electrogalvanized E-60 and 6061 aluminum. In contrast to the
example in U.S. Pat. No. 5,868,820, the coating was applied at 25
degrees.
[0064] The panels thereafter were coated with the PPG powder
coating PCT 50113 (available from PPG Industries, Inc.), cured,
scribed, and subjected to salt fog corrosion testing according to
ASTM B117. The test duration was 168 hours for CRS, 384 hours for
electrogalvanized, and 1000 hours for aluminum. The paint losses in
mm by delamination from taping are set forth in Table 1.
2 TABLE 1 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 8
Electrogalvanized 4.5 Aluminum 6061 2.5
Example 2
[0065] This example also represents a comparative example, relating
to a coating composition prepared according to the teachings of
Example 3 of U.S. Pat. No. 5,868,820.
[0066] The reactive coating bath was prepared as in Example 1, but
with NaClO.sub.3 replaced by 7 grams of sodium meta-nitrobenzene
sulfonate, resulting in concentrations as follows:
3 COMPONENT CONCENTRATION, ppm Phosphoric Acid 18,000 NaOH 4,000
Sodium meta-nitrobenzene sulfonate 7,000 Ammonium Bifluoride 700
Tannin 3,000
[0067] Panels were coated, painted and tested in a similar manner
as in Example 1. In particular, the conversion coating was applied
at 25 degrees, in contrast to Example 3 of U.S. Pat. No. 5,868,820.
The results are set forth in Table 2A.
4 TABLE 2A SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 7
Electrogalvanized E-60 4 Aluminum 6061 2.5
[0068] A second set of panels was treated with the same organic
conversion coating and then subjected to a zirconium rinse with a
solution of fluorozirconic acid at a concentration of 175 ppm of
Zr. The panels were painted, cured, scribed and tested as before,
with the results set forth in Table 2B.
5 TABLE 2B SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 6
Electrogalvanized E-60 4 Aluminum 6061 1.5
[0069] As is apparent from a comparison of the results in Tables 2A
and 2B, the zirconium rinse provides little, if any, benefit to
adhesion.
Example 3
[0070] This example represents a comparative example, relating to a
coating composition prepared according to the teachings of Example
1 of U.S. Pat. No. 4,338,140.
[0071] In particular, a bath was prepared to contain the
following:
6 COMPONENT CONCENTRATION, ppm H.sub.2TiF.sub.6 168
NH.sub.4H.sub.2PO.sub.4 143 H.sub.2C.sub.6H.sub.60.sub.7 46 Tannic
Acid 30 NH.sub.4HCO.sub.3 411 HNO.sub.3 588 PH 2.5
[0072] Panels were coated, painted and tested in a similar manner
as in Example 1, with the results set forth in Table 3:
7 TABLE 3 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 12 Hot Dip
Galvanized G-90 2 Electrogalvanized E-60 1
Example 4
[0073] This example represents a coating composition prepared
according to the present invention.
[0074] A bath was made as in Example 1, band further including 175
ppm zirconium as fluorozirconic acid.
[0075] The organic conversion coating composition as prepared was
applied to individual panels of cold rolled steel, hot dip
galvanized G-90, and electrogalvanized E-60. The organic conversion
coating composition was applied by spray at 25.degree. C. for 60
seconds spray time.
[0076] The thus coated panels of cold rolled steel, hot dip
galvanized G-90, and electrogalvanized E-60 were painted with a
solvent based polyester white paint (PLOYCRON 1000 of PPG
Industries, Inc.) Each of these panels was then cured, scribed and
subjected to salt fog corrosion testing per ASTM B-117. The paint
losses in mm by delamination from taping after 96 hours are set
forth in Table 4.
8 TABLE 4 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 1 Hot Dip
Galvanized G-90 1 Electrogalvanized E-60 0
[0077] A comparison of the results of Examples 1, 2 and 4
demonstrate the improvements seen through the present
invention.
Example 5
[0078] The reactive organic conversion coating composition of
Example 4 was prepared, with the zirconium replaced with 92 ppm of
titanium as hexafluorotitanate. The reactive organic conversion
coating composition as prepared was applied, subsequently painted,
and tested as set forth in Example 4. The results are shown in
Table 5.
9 TABLE 5 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 2 Hot Dip
Galvanized G-90 1 Electrogalvanized E-60 1
[0079] As is apparent, titanium may be substituted for zirconium
with similar improvements in performance.
Example 6
[0080] The reactive organic conversion coating composition of
Example 4 was again prepared, with the amount of tannin decreased
to a concentration of 70 ppm. The reactive organic conversion
coating composition as prepared was applied, subsequently painted,
and tested as set forth in Example 4. The results are shown in
Table 6.
10 TABLE 6 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 12 Hot Dip
Galvanized G-90 5 Electrogalvanized E-60 20
Example 7
[0081] The reactive organic conversion coating composition of
Example 5 was prepared including hexafluorotitanate, with the
amount of tannin decreased to a concentration of 70 ppm. The
reactive organic conversion coating composition as prepared was
applied, subsequently painted, and tested as set forth in Example
4. The results are shown in Table 7.
11 TABLE 7 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 15 Hot Dip
Galvanized G-90 6 Electrogalvanized E-60 20
[0082] A-comparison of the results of Examples 6 and 7 with the
results of Examples 4 and 5 demonstrates that higher levels of
tannin are required to provide the improved results seen through
the present invention.
Example 8
[0083] The reactive organic conversion coating composition of
Example 4 was prepared as set forth in Example 4. A first set of
panels was coated with the bath as set forth in Example 4, and a
second set of panels was coated in a similar manner, after a period
of spraying of the bath for 45 minutes. Following this application,
the two sets of panels were painted and tested as set forth in
Example 4. The results are shown in Table 8.
12TABLE 8 PAINT LOSS - mm SUBSTRATE New Bath Bath aged 45 minutes
Cold Rolled Steel 1 7 Hot Dip Galvanized G-90 1 1 Electrogalvanized
E-60 1 1
Example 9
[0084] Example 8 was repeated, with 6 grams per liter of lactose
added to the bath prior to coating of the panels. Three sets of
panels were coated with the bath, representing a new bath, after a
period of spraying of the bath for 45 minutes, and after a period
of spraying of the bath for 90 minutes, respectively. Following
this application, the three sets of panels were painted and tested
as set forth in Example 4. The results are shown in Table 9.
13TABLE 9 PAINT LOSS - mm Bath aged Bath aged SUBSTRATE New Bath 45
minutes 90 minutes Cold Rolled Steel 1 1 1 Hot Dip Galvanized G-90
1 1 1 Electrogalvanized E-60 1 1 1
[0085] A comparison of the results of Examples 8 and 9 demonstrates
that the addition of the disaccharide lactose has an affect on the
age of the bath. In Example 8, the panels coated with the bath
after aging for 45 minutes showed reduced adhesion as compared with
a new bath. In Example 9, however, the panels coated with the bath
after aging for 45 minutes and even 90 minutes showed no reduction
in adhesion.
Example 10
[0086] The reactive organic conversion coating composition of
Example 4 was prepared, with the hexafluorozirconate replaced with
175 ppm Zr as ammonium pentafluorozirconate (prepared from the
decomposition of ammonium hexafluorozirconate). The reactive
organic conversion coating composition as prepared was applied,
subsequently painted, and tested as set forth in Example 4. The
results are shown in Table 10.
14 TABLE 10 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 1 Hot Dip
Galvanized G-90 1 Electrogalvanized E-60 0
[0087] A comparison of the results of Example 10 with those of
Example 4 demonstrate that reactive organic conversion coatings
prepared with pentafluorozirconates perform in a similar manner as
those prepared with hexafluorozirconates.
Example 11
[0088] The reactive organic conversion coating composition of
Example 4 was prepared and applied as set forth in Example 4.
Following this application, the panels were subsequently coated
with a 1% aqueous solution of a triethoxy ester of n-propyl
gamma-amino silane (available commercially as Z-6011 from Dow
Corning) for 30 seconds. The panels were then air dried, painted
and tested as set forth in Example 4. The results are shown in
Table 11.
15 TABLE 11 SUBSTRATE PAINT LOSS - mm Cold Rolled Steel 0 Hot Dip
Galvanized G-90 0 Electrogalvanized E-60 0
[0089] While the invention has been described in terms of preferred
embodiments, it is to be understood that various modifications
thereof will become apparent to those skilled in the art upon
reading the specification. Therefore, it is to be understood that
the invention disclosed herein is intended to encompass such
modifications as fall within the scope of the appended claims.
* * * * *