EP1109852A1 - Water washable protective coating - Google Patents

Water washable protective coating

Info

Publication number
EP1109852A1
EP1109852A1 EP98944534A EP98944534A EP1109852A1 EP 1109852 A1 EP1109852 A1 EP 1109852A1 EP 98944534 A EP98944534 A EP 98944534A EP 98944534 A EP98944534 A EP 98944534A EP 1109852 A1 EP1109852 A1 EP 1109852A1
Authority
EP
European Patent Office
Prior art keywords
composition
range
weight
coating
water
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Withdrawn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
EP98944534A
Other languages
German (de)
French (fr)
Other versions
EP1109852A4 (en
Inventor
Jeffrey Maxwell
George Saquet
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.)
Gage Products Co
Original Assignee
Gage Products Co
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
Priority claimed from US09/139,818 external-priority patent/US6011107A/en
Application filed by Gage Products Co filed Critical Gage Products Co
Priority claimed from PCT/US1998/017681 external-priority patent/WO1999010414A1/en
Publication of EP1109852A1 publication Critical patent/EP1109852A1/en
Publication of EP1109852A4 publication Critical patent/EP1109852A4/en
Withdrawn legal-status Critical Current

Links

Definitions

  • This invention relates generally to polymeric coatings. More particularly,
  • the invention relates to an acrylic based protective coating which can be deposited
  • Protective coatings typically comprise formulations including waxes,
  • the present invention provides a
  • polymers As is known in the art, such materials include polymers of acrylic acid
  • a near neutral pH refers to
  • the protective coatings of the present invention are applied from an
  • compositions of the invention which has a pH in the range of 7.5-9.5.
  • present invention may be applied by spraying, brushing, dipping or any other such coating technique.
  • the final properties of the coating may be adjusted for various
  • relatively low temperature conditions may be made relatively soft so as to resist cracking, while coatings which will be employed in high temperature conditions
  • Acrylic based materials have previously been employed in a variety of coating applications; however, it has been found, in accord with the present
  • present will include, on a weight basis, approximately 10-50% of a mix of at least
  • the polymers are mixed with water, and an alkali, such as sodium hydroxide, potassium hydroxide or mixtures thereof, in an amount,
  • composition ranging from 0.5 to 2.5%, by weight, sufficient to maintain the composition at a pH of 7.5 to 9.5.
  • the composition are characterized in
  • the glass transition temperature of a coating produced by the evaporation of water from the composition is in the range of 0-
  • polymers includes a first polymer having a molecular weight of no more than
  • styrene acrylic copolymer sold by the B.F.
  • Carboset® 1 161 or 1162 The
  • alkaline pHs typically in the range of 8.0 - 9.5. This is an important feature of the
  • the low molecular weight, high acid number acrylic resin serves to decrease the viscosity of the resultant solution, permitting the use of high solids formulations.
  • the low molecular weight, high acid number acrylic resin serves to decrease the viscosity of the resultant solution, permitting the use of high solids formulations.
  • present invention will also include a higher molecular weight, lower acid number
  • weight of the resultant composition is at least approximately 35,000.
  • a coating composition for depositing a protective layer comprises, by weight, 10-50% of a mixture of at
  • the composition includes water and an alkali in an amount sufficient to maintain the composition at a pH in the range of 7.5 to 9.5.
  • mixture of at least two acrylic polymers is in the range of 35,000 to 100,000, the
  • average acid number of the mixture is in the range of 65 to 150, and the glass
  • transition temperature of a coating produced by the evaporation of the water from the composition is in the range of 0 to 70 °C.
  • hydroxide and sodium hydroxide are included in the coating composition in an
  • the glass transition temperature of the coating composition preferably ranges from approximately 0 to 10°C. Most preferably, the glass transition temperature of the coating composition is in the range of approximately
  • 1019-118A comprises, by weight, approximately 6.00% Carboset 525 resin, approximately 9.1%) Carboset 515 resin, approximately 0.6% sodium hydroxide,
  • the water is preferably heated to 70-80°C.
  • the water is preferably heated to 70-80°C.
  • the composition includes approximately 0.27% of a water softening ion chelating agent sold by the Ashland Corporation under the trade name Versene
  • composition can be applied to an article by spraying, dipping, or brushing, and is
  • the overall Tg of the resultant film is approximately 4°C and the
  • average molecular weight of the resin in the film is approximately 87,000.
  • compositions along with a Tg in the range of approximately 0-8 °C are critical to eliminating the etching and distortion problem discussed above.
  • depositing a protective layer comprises, by weight, 1-5% of a first acrylic polymer
  • the composition includes a second acrylic polymer, in an amount of 6-
  • this second acrylic polymer has a molecular weight in the range of
  • composition also includes a third acrylic polymer, in an amount of approximately
  • this third acrylic polymer has a molecular weight in the range of
  • the composition also includes 3-10% of a fourth acrylic polymer having a molecular weight in the range of 5,000-10,000, an acid number in the range of 50-70 and a Tg of less than 0°C.
  • a fourth acrylic polymer having a molecular weight in the range of 5,000-10,000, an acid number in the range of 50-70 and a Tg of less than 0°C.
  • an alkali such as sodium hydroxide, potassium
  • the viscosity of the coating compositions will depend upon the particular solvent used for the coating compositions.
  • composition in one embodiment, includes, by weight, approximately 10-30%) of the foregoing acrylic resins.
  • weight in one particularly preferred embodiment, includes, by weight, approximately 10-30%) of the foregoing acrylic resins.
  • the resins collectively total 20% by weight of the composition.
  • compositions may further include other,
  • ancillary ingredients such as water softening agents, chelating agents, surfactants and the like. These materials are typically present in relatively small amounts such as 0.1-1.0%.
  • the composition may also include other ancillary ingredients such as water softening agents, chelating agents, surfactants and the like.
  • U.V. blocking agents as U.V. blocking agents, biocides, fungicides, defoamers, fragrances and colors.
  • the wax is typically employed as an approximately 50% emulsion in water, and
  • this emulsion is present in a weight amount of approximately 0.5-2.0% of the composition.
  • One group of materials comprises styrene-
  • acrylic copolymers also referred to as a styrenated acrylics
  • Carboset the B.F. Goodrich corporation under the designation Carboset. These materials are available in various grades; and Carboset 526 may be advantageously
  • Carboset 1161 or 1162 may be employed as the first acrylic polymer
  • Carboset 525 may be employed as the third acrylic polymer
  • Carboset 515 may be employed as the fourth acrylic polymer.
  • composition of the present invention comprises, by weight, 1.2% Carboset 526 resin, 9.0% Carboset 1161 resin, 4.0% Carboset
  • Carboset 515 resin Carboset 515 resin.
  • the resins are dissolved in deionized water, in an amount of 79% of the composition.
  • the water is preferably heated
  • the composition includes 0.3% of water softening and
  • compositions may be applied to an article by spraying
  • the resultant film is durable and scratch resistant.
  • the overall Tg of the resultant film is approximately 53 °C and the average molecular weight of the
  • resin in the film is approximately 59,000.
  • composition of the present invention comprises, on a
  • Carboset 527 resin 2.38% Carboset 1162 resin; 7.94% Carboset 1161 resin;
  • deionized water in an amount of 69.21%) of the composition and the water includes 2.67%> by weight of sodium hydroxide.
  • Another coating composition comprises, on a weight basis, 2.89% Carboset 525 resin; 0.87%) Carboset 526 resin; 8.67% Carboset 1161 resin and
  • Carboset 515 resin 3.92%) Carboset 515 resin.
  • the resins are dissolved in 80.72%> de-ionized water,
  • composition also includes 0.36%
  • This particular composition also includes 0.23% of an ultra-violet light absorbing agent sold under the designation Tinuvin 1130, and 0.24%> of an anti ⁇
  • the average molecular weight of the resultant composition is approximately 41719, and the glass transition temperature of the resultant film produced thereby is calculated
  • Carboset 525 resin will harden the film. It has also been found that
  • the viscosity can be adjusted by varying the relative amounts of the resin
  • the pH can be adjusted by adjusting the concentration of alkali in
  • compositions include Carboset resins, sold by the B.F. Goodrich Corporation, similar resins are available from other suppliers, and may be employed in the present invention. Also, as noted above,
  • a relatively small amount of wax emulsion may be added to the material to
  • drying time of the film can be decreased by replacing up
  • Panels are rinsed under room temperature water for up to five minutes and then blown off with air after exposures
  • Exposure 336 hours at 82 ⁇ 2 °C Exposure Chamber: Despatch LDB 2-27-4 Oven (ACT #207)
  • Exposure Chamber Atlas UV-CON Cabinet (ACT #52) Examinations: Visual examination for marring, cracking, discoloration, etc. Removability QUV Exposure Test Data:
  • Procedure Apply 0.05 mL of test solution to each panel. Leave at room temperature for 30 minutes, then place in preheated chambers at specified temperatures for 30 minutes. Remove material and evaluate.
  • Test Temperatures 50 ⁇ 2°C, 60 ⁇ 2°C, 70 ⁇ 2°C, 80 ⁇ 2°C
  • Test Materials A - G-2000 Batch #20528 undiluted - See Table 1
  • test materials C and D did not cause swelling of the underlying clearcoat over which materials C and D were applied.
  • Materials C and D correspond to Formulation 1019-118A of Table 1.
  • This formulation includes both potassium hydroxide and sodium hydroxide, has a Tg of approximately 4 and an average molecular weight of approximately 87,000.
  • motor vehicles may be easily applied to cover the painted and plated

Landscapes

  • Paints Or Removers (AREA)

Abstract

A coating composition for producing a water washable, protective coating, comprising, by weight, 10-50 % of a mixture of at least two acrylic polymers each having different molecular weights, acid numbers, and glass transition temperatures. The composition includes water and an alkali, in an amount sufficient to maintain the composition at a pH in the range of 7.5 to 9.5 and is further characterized in that the average molecular weight of the mixture of the at least two acrylic polymers is in the range of approximately 35,000 to 100,000. The average acid number of the mixture is in the range of approximately 65 to 150 and the glass transition temperature of a coating produced by the evaporation of the water from the composition is in the range of 0 to 70 °C.

Description

WATERWASHABLE PROTECTIVE COATING
This application claims priority of United States Provisional Application
No. 60/057,359 filed August 26, 1997.
Field of the Invention This invention relates generally to polymeric coatings. More particularly,
the invention relates to an acrylic based protective coating which can be deposited
from an aqueous solution, and which may be removed from an article by washing with neutral pH water.
Background of the Invention Protective coatings are applied to automobiles and other articles to protect
their surface finishes from dirt, scratches and other damage occurring during
manufacture, shipping and storage. Such coatings should be tough, easy to apply,
easy to remove and should not cause any harm to the article to which they are applied. Protective coatings typically comprise formulations including waxes,
polymers and the like. Most of such coatings are deposited from compositions
including organic solvents therein. Removal of these coatings requires either organic solvents or wash water having a relatively alkaline pH. Organic solvents
or non-neutral aqueous solutions can cause damage to various articles of
manufacture, and complicate the formulation and handling of such coatings.
In addition to not causing harm to the article to which they are applied,
protective coatings, particularly when applied over a clearcoat layer applied over
a paint layer, must also resist etching and distorting the clearcoat layer following
the exposure or application of heat to the protective coating. This situation commonly arises during the application of trim components such as pin-striping
when heat is applied directly to the protective coating in order to facilitate the
adhesion of pin-striping to the surface of the automobile or when an automobile leaves the assembly plant without first having the protective coating removed and
is then exposed to heating by sunlight. Automobile manufacturers, therefore,
require that these protective coatings resist chemical etching and distortion of the
underlying clearcoat of the automobile upon exposure to heat.
Accordingly, there is a need for a protective coating formulation which is aqueous based, and which has a neutral or near neutral pH. It is further desirable
that this formulation provide a tough, durable, protective coating, but that the
coating be removable from the surface by washing with neutral or near neutral pH water. It would be further desirable and advantageous to have a protective coating which will not etch nor distort the underlying clearcoat layer following exposure
to heat. As will be described hereinbelow, the present invention provides a
composition fulfilling these criteria.
Detailed Description of the Invention The protective coatings of the present invention are based upon acrylic
polymers. As is known in the art, such materials include polymers of acrylic acid
as well as substituted acrylic acids such as methyl methacrylate, as well as
copolymers such as styrene acrylic copolymers, and the like. The coatings of the
present invention are durable, and resistant to ambient humidity; however, they are readily removed from a surface by washing with water having a neutral, or near neutral, pH. In the context of the present disclosure, a near neutral pH refers to
water having a pH which is only slightly acid or slightly alkaline. Generally, a
near neutral pH is in the range of 4.5-9.5. It should also be noted that all
formulations given herein are specified on a weight basis.
The protective coatings of the present invention are applied from an
aqueous solution which has a pH in the range of 7.5-9.5. The compositions of the
present invention may be applied by spraying, brushing, dipping or any other such coating technique. The final properties of the coating may be adjusted for various
applications. In those instances where a relatively thick coating is required, a
higher viscosity coating solution is employed. Coatings which will encounter
relatively low temperature conditions may be made relatively soft so as to resist cracking, while coatings which will be employed in high temperature conditions
may be made to have a relatively high glass transition temperature, so that they
will retain film strength at elevated temperatures.
Acrylic based materials have previously been employed in a variety of coating applications; however, it has been found, in accord with the present
invention, that superior results are achieved when a protective coating is prepared
from a blend of acrylic polymers, having different molecular weights, acid
numbers and glass transition temperatures. Preferably, the composition of the
present will include, on a weight basis, approximately 10-50% of a mix of at least
two acrylic polymers having different molecular weights, acid numbers and glass
transition temperatures. The polymers are mixed with water, and an alkali, such as sodium hydroxide, potassium hydroxide or mixtures thereof, in an amount,
ranging from 0.5 to 2.5%, by weight, sufficient to maintain the composition at a pH of 7.5 to 9.5. In particular embodiments, the composition are characterized in
that the average molecular weight of the polymers comprising the mixture is in the
range of approximately 35,000 to 100,000, and the average acid number of the mix
is in the range of 65-150, and the glass transition temperature of a coating produced by the evaporation of water from the composition is in the range of 0-
70°C.
In some particular embodiments of the invention, the mix of acrylic
polymers includes a first polymer having a molecular weight of no more than
2,000 and an acid number of at least 180, and more preferably 200. One example of such materials comprises the styrene acrylic copolymer sold by the B.F.
Goodrich Corporation under the designation Carboset® 1 161 or 1162. The
aqueous solutions of these materials exhibit a decrease in viscosity at mildly
alkaline pHs, typically in the range of 8.0 - 9.5. This is an important feature of the
present invention, because viscosity is often a limiting factor in determining the
total solids content in coating compositions. Generally, users wish to have a high
solids composition so as to minimize the amount of solution handled, and drying
time; however, high solids compositions often have very high viscosities preventing them from being readily applied in conventional coating processes. It
has been found that inclusion of the low molecular, high acid number polymers
serves to decrease the viscosity of the resultant solution, permitting the use of high solids formulations. The low molecular weight, high acid number acrylic
polymers are not good film formers, and for this reason, the compositions of the
present invention will also include a higher molecular weight, lower acid number
film forming polymer, in an amount sufficient such that the average molecular
weight of the resultant composition is at least approximately 35,000.
In a preferred embodiment of the present invention, a coating composition for depositing a protective layer comprises, by weight, 10-50% of a mixture of at
least two acrylic polymers having different molecular weights, acid numbers, and
glass transition temperatures. The composition includes water and an alkali in an amount sufficient to maintain the composition at a pH in the range of 7.5 to 9.5.
The composition is characterized in that the average molecular weight of the
mixture of at least two acrylic polymers is in the range of 35,000 to 100,000, the
average acid number of the mixture is in the range of 65 to 150, and the glass
transition temperature of a coating produced by the evaporation of the water from the composition is in the range of 0 to 70 °C. The alkali utilized in this
embodiment preferably includes potassium hydroxide in an amount ranging from
approximately 0.5-2.50%, by weight, of the composition. Additionally, the alkali
can be sodium hydroxide in an amount ranging from approximately 0.5-2.50%), by
weight, of the composition. In a most preferred embodiment, both potassium
hydroxide and sodium hydroxide are included in the coating composition in an
amount ranging from approximately 0.5-2.50%, by weight, of the composition.
In this embodiment, the glass transition temperature of the coating composition preferably ranges from approximately 0 to 10°C. Most preferably, the glass transition temperature of the coating composition is in the range of approximately
3 to 8°C. This embodiment of the present invention, referred to in Table 1 as
1019-118A, comprises, by weight, approximately 6.00% Carboset 525 resin, approximately 9.1%) Carboset 515 resin, approximately 0.6% sodium hydroxide,
and approximately 0.63% potassium hydroxide. The resins and alkali are
dissolved in deionized water, in an amount of approximately 83% of the
composition. The water is preferably heated to 70-80°C. In addition to the
foregoing, the composition includes approximately 0.27% of a water softening ion chelating agent sold by the Ashland Corporation under the trade name Versene
100, approximately 0.3%> of sodium lauryl sulfate, and approximately 0.02%) of
an anti-foaming agent sold under the trade name Foamaster 111. The resultant
composition can be applied to an article by spraying, dipping, or brushing, and is
subsequently dried to remove the water solvent to yield a durable and scratch
resistant film. The overall Tg of the resultant film is approximately 4°C and the
average molecular weight of the resin in the film is approximately 87,000.
Applicants have found that both the addition of potassium to the
composition along with a Tg in the range of approximately 0-8 °C are critical to eliminating the etching and distortion problem discussed above. Table 1
illustrates several embodiments of the subject coating composition. Table 1
In another embodiment of the present invention, a coating composition for
depositing a protective layer comprises, by weight, 1-5% of a first acrylic polymer
which has a molecular weight in the range of 125,000 to 175,000, an acid number
in the range of 80-120 and a glass transition temperature (Tg) in the range of 60- 80 °C. The composition includes a second acrylic polymer, in an amount of 6-
15%, and this second acrylic polymer has a molecular weight in the range of
1,000-2,000, an acid number of 180-230 and a Tg in the range of 70-110. The
composition also includes a third acrylic polymer, in an amount of approximately
3-10%; and this third acrylic polymer has a molecular weight in the range of
175,000-250,000, an acid number of approximately 60-90, and a Tg in the range
of 20-50. The composition also includes 3-10% of a fourth acrylic polymer having a molecular weight in the range of 5,000-10,000, an acid number in the range of 50-70 and a Tg of less than 0°C. The foregoing acrylic polymers are
dissolved in water, together with an alkali, such as sodium hydroxide, potassium
hydroxide, ammonia, triethanolamine or the like, in an amount sufficient to
solubilize the polymers and maintain the composition at a pH in the range of 7.5- 9.5.
The viscosity of the coating compositions will depend upon the particular
application; but, typical viscosities are in the range of 30-1500 centipoise at 20°C,
as measured by a Brookfield viscometer using a #1 spindle at 50 rpm.
The composition, in one embodiment, includes, by weight, approximately 10-30%) of the foregoing acrylic resins. In one particularly preferred embodiment,
the resins collectively total 20% by weight of the composition.
Any of the above-described compositions may further include other,
ancillary ingredients such as water softening agents, chelating agents, surfactants and the like. These materials are typically present in relatively small amounts such as 0.1-1.0%. The composition may also include other ancillary ingredients such
as U.V. blocking agents, biocides, fungicides, defoamers, fragrances and colors.
In accord with the present invention, it has been found that the addition of a relatively small amount of emulsified wax enhances the resistance of the dried
film to ambient humidity, but does not adversely affect rinsibility of the dried film.
The wax is typically employed as an approximately 50% emulsion in water, and
this emulsion is present in a weight amount of approximately 0.5-2.0% of the composition.
There are a variety of acrylic polymers which may be employed in the
practice of the present invention. One group of materials comprises styrene-
acrylic copolymers (also referred to as a styrenated acrylics) such as those sold by
the B.F. Goodrich corporation under the designation Carboset. These materials are available in various grades; and Carboset 526 may be advantageously
employed as the first acrylic polymer; Carboset 1161 or 1162 may be employed
as the second acrylic polymer; Carboset 525 may be employed as the third acrylic polymer, and Carboset 515 may be employed as the fourth acrylic polymer. Other
similar materials are available from the S.C. Johnson corporation under the
designation Joncryl, or from ICI Inc. under the name Zeneca. Other polymer
suppliers such as R om & Haas and Rhone-Poulenc also sell similar materials.
One illustrative, embodied composition of the present invention comprises, by weight, 1.2% Carboset 526 resin, 9.0% Carboset 1161 resin, 4.0% Carboset
525 resin, and 4.0%) Carboset 515 resin. The resins are dissolved in deionized water, in an amount of 79% of the composition. The water is preferably heated
to 70-80°C, and includes approximately 2.2% by weight of the composition of a
50%> solution of sodium hydroxide to facilitate dissolution of the resins, and to
maintain the pH of the resultant solution in the range of approximately 7.5-9.5.
In addition to the foregoing, the composition includes 0.3% of water softening and
ion chelating agent sold by the Ashland corporation under the designation Versene 100, and 0.3%) of sodium lauryl sulfate, which is used as a wetting agent and rinse
aid.
The foregoing compositions may be applied to an article by spraying,
dipping or brushing, and is subsequently dried to remove the water solvent therefrom. The resultant film is durable and scratch resistant. The overall Tg of the resultant film is approximately 53 °C and the average molecular weight of the
resin in the film is approximately 59,000.
Another embodied composition of the present invention comprises, on a
weight basis, 2.38% Carboset 525 resin; 1.59% Carboset 526 resin; 3.97%
Carboset 527 resin; 2.38% Carboset 1162 resin; 7.94% Carboset 1161 resin;
6.59% Carboset 515 resin; 0.27% sodium lauryl sulfate surfactant and .36% of the
above-referenced Versene 100 water softening agent. The resins are dissolved in
deionized water in an amount of 69.21%) of the composition and the water includes 2.67%> by weight of sodium hydroxide. The average molecular weight
of this composition is approximately 38,000, and the glass transition temperature
of the resultant dried film is calculated to be approximately 40°C. Another coating composition comprises, on a weight basis, 2.89% Carboset 525 resin; 0.87%) Carboset 526 resin; 8.67% Carboset 1161 resin and
3.92%) Carboset 515 resin. The resins are dissolved in 80.72%> de-ionized water,
along with 1.82% sodium hydroxide. The composition also includes 0.36%
Versene 100 water softening agent and 0.28% sodium lauryl sulfate, as in previous
examples. This particular composition also includes 0.23% of an ultra-violet light absorbing agent sold under the designation Tinuvin 1130, and 0.24%> of an anti¬
bacterial agent sold under the designation CS-1135. These last two agents
increase the stability of the resultant film to ambient conditions. The average molecular weight of the resultant composition is approximately 41719, and the glass transition temperature of the resultant film produced thereby is calculated
to be approximately 50°C.
As noted above, the proportions of the various resins may be varied within
the listed ranges so as to adjust the overall performance of the film. For example, increase in the amount of the low molecular weight Carboset 515 resin will soften
the resultant film, while increasing the amount of the relatively high molecular
weight Carboset 525 resin will harden the film. It has also been found that
substituting Carboset 1162 for Carboset 1161 will produce a somewhat harder
film, more useful for high temperature applications. Also, it has been found that
the viscosity can be adjusted by varying the relative amounts of the resin
components. The pH can be adjusted by adjusting the concentration of alkali in
the composition. While the foregoing compositions include Carboset resins, sold by the B.F. Goodrich Corporation, similar resins are available from other suppliers, and may be employed in the present invention. Also, as noted above,
a relatively small amount of wax emulsion may be added to the material to
enhance resistance to humidity. Surprisingly enough, addition of this emulsion does not detract from the water rinsibility of the film.
In addition, the drying time of the film can be decreased by replacing up
to half of the water with an alcohol such as isopropanol or ethanol.
The following examples are given for the purpose of illustrating various
embodiments of the invention and are not meant to limit the present invention in any way.
EXAMPLES
Example 1 - Removability of Coating from an Article
Standard: GM 9982223 04/94 Material: G-2000 Anti-Scratch Coating Batch #20528 - See Table 1 for Composition
Paint System Identification:
A. Phosphate: B952 P60 B: Phosphate: B952 P60 ECoat: ED5000 ECoat: ED5050A Basecoat: 542AB921 Black Basecoat: 408AB921 Black Clearcoat: RK 8010 Gen 4A Clearcoat: RK8018
Transit Film Build Conditions:
Normal = N Low = L High = H Removal Procedure:
Panels are rinsed under room temperature water for up to five minutes and then blown off with air after exposures
Evaluation 3.3.1: Moisture Resistance
Test Method: GM 4465P 07/95 Exposure: 96 Hours Recovery: 24 Hours Exposure Chamber: Singleton Model 24 (ACT #87)
Examination: Visual examination for loss of film integrity of softening
Rating Scale: 0 = No effect (etching) from contaminants
1 = Trace/slight effect
2 = Moderate effect
3 = Pronounced/severe effect
Moisture Resistance Test Data:
ID Film Integrity Softening
A1N No transit film remaining n/a BIN No transit film remaining n/a
The results of this example demonstrate that a film coating in accordance with the invention can be rinsed from an article with water.
Example 2 - Discoloration or Cracking
Standard: GM 9982223 04/94 Material: G-2000 Anti-Scratch Coating Batch #20528 - See Table 1 for Composition
Evaluation 3.3.2: Heat Age
Exposure: 336 hours at 82 ± 2 °C Exposure Chamber: Despatch LDB 2-27-4 Oven (ACT #207)
Examinations: Visual examination for discoloration or cracking Removability Rating Scale: 0 = No effect (etching) from contaminants
1 = Trace/slight effect
2 = Moderate effect
3 = Pronounced/severe effect
Heat Age Test Data:
ID Visual Change Removability
AIL 0 0
A1N 0 0 A1H 0 0
B1L 0 0 BIN 0 0 B1H 0 0
The results of this example demonstrate that a coating in accordance with the present invention was removable and did not discolor an article after prolonged exposure to heat.
Example 3 - Resistance to Changes in the Coated Film Due to U.V. Exposure
Evaluation 3.3.7: QUV Exposure Test Method: GM 9125P 07/91 Material: G-2000 Anti-Scratch Coating Batch #20528 - See
Table 1 for Composition
Cycle: 8 hours UV at 70 ± 2°C
4 hours condensation at 50 ± 2°C
Exposure 250 and 500 hours
Exposure Chamber: Atlas UV-CON Cabinet (ACT #52) Examinations: Visual examination for marring, cracking, discoloration, etc. Removability QUV Exposure Test Data:
ID Exposure Visual Change Removabilitv
A1N 250 Hours 0 *
A1H 250 Hours 0 *
BIN 250 Hours 0 *
B1H 250 Hours 0 *
A1N 500 Hours 0 *
A1H 500 Hours 0 *
BIN 500 Hours 0 *
B1H 500 Hours 0 *
*No transit film remained on the panels after exposure
The results illustrated in this example demonstrate that a coating composition in accordance with the present invention resists changes due to prolonged UN. light exposure.
Example 4 - Resistance to Chemical Etching
Evaluation #4: Resistance to Chemical Etching
Test Method: GM 9533P 07/95 Method 3 Material: G-2000 Anti-Scratch Coating Batch #20528 - See
Table 1 for Composition
Procedure: Apply 0.05 mL of test solution to each panel. Leave at room temperature for 30 minutes, then place in preheated chambers at specified temperatures for 30 minutes. Remove material and evaluate.
Test Temperatures: 50 ± 2°C, 60 ± 2°C, 70 ± 2°C, 80 ± 2°C
50 °C Chamber Cincinnati Sub Zero (ACT #579)
60 °C Chamber Hotpack (ACT #7) 70 °C Chamber Thermotron Model SM-32C (ACT #175) 80 °C Chamber Thermotron Model SM-32C (ACT #26)
Examination: Visual examination for change Degree of Change: None: No change
Slight: Barely observable with normal examination Moderate: Modest change, Readily noticeable Pronounced: Distinct change, Easily observed with casual examination
Test Materials: A - G-2000 Batch #20528 undiluted - See Table 1
B - G-2000 Batch #20528 diluted with deionized water to 10% non-volatiles
C - G-2000 Batch #10191 18A undiluted - See Table 1
D - G-2000 Batch #1019118A diluted with deionized water to 10% non-volatiles
E - Competitor's material from Ford Kentucky Truck Plant 1/15/98 undiluted
Competitor's material from Ford Kentucky Truck Plant 1/15/98 diluted with deionized water to 10% non-volatiles
G - Deionized Water
Resistance to Chemical Etching Test Data:
Paint System Temperature Material A Material B Material C A 50°C Slight Swelling Slight Swelling No Change B 50°C Slight Swelling Slight Swelling No Change
A 60° Slight Swelling Slight Swelling No Change B 60° Slight Swelling Slight Swelling No Change
A 70° Slight Swelling Slight Swelling No Change B 70° Slight Swelling Slight Swelling No Change
A 80° Slight Swelling Slight Swelling No Change B 80° Slight Swelling Slight Swelling No Change Paint Svstem Temperature Material D Material E Material F A 50°C No Change Slight Swelling Slight Swelling B 50°C No Change Slight Swelling Slight Swelling
A 60° No Change Slight Swelling Slight Swelling B 60° No Change Slight Swelling Slight Swelling
A 70° No Change Slight Swelling Slight Swelling B 70° No Change Slight Swelling Slight Swelling
A 80° No Change Slight Swelling Slight Swelling B 80° No Change Slight Swelling Slight Swelling
Paint Svstem Temperature Material G A 50°C No Change B 50°C No Change
A 60° No Change B 60° No Change
A 70° No Change B 70° No Change
A 80° No Change B 80° No Change
Note - No etching was observed at any condition
The results of this example demonstrate that test materials C and D did not cause swelling of the underlying clearcoat over which materials C and D were applied. Materials C and D correspond to Formulation 1019-118A of Table 1. This formulation includes both potassium hydroxide and sodium hydroxide, has a Tg of approximately 4 and an average molecular weight of approximately 87,000.
The aforedescribed materials have significant utility in the manufacture of
motor vehicles. They may be easily applied to cover the painted and plated
portions of the vehicle, and their durability protects the finish from scratches
during assembly. At final stage in their assembly, most motor vehicles are subjected to a water wash for the purpose of testing their water tightness, and this
water wash will function to remove the protective coating.
While some specific formulations have been disclosed herein, it is to be
understood that other variations and modifications of the aforedescribed compositions may be implemented in accord with the present invention. The foregoing are illustrative of particular embodiments, but not meant to be
limitations upon the practice thereof. It is the following claims, including all
equivalents, which define the scope of the invention.

Claims

Claims
1. A coating composition for producing a water washable, protective
coating, said composition comprising, by weight: 10-50% of a mixture of at least two acrylic polymers, said polymers having
different molecular weights, acid numbers and glass transition temperatures;
water; and
an alkali, in an amount sufficient to maintain the composition at a pH in
the range of 7.5 to 9.5, said composition further characterized in that the average molecular weight of said mixture of at least two acrylic polymers is in the range of 35,000 to 100,000, the average acid number of said mixture is in the range of
65 to 150, and the glass transition temperature of a coating produced by the
evaporation of the water from said composition is in the range 0 to 70°C.
2. A composition as in claim 1 , wherein said alkali includes potassium hydroxide.
3. A composition as in claim 1, wherein said alkali includes sodium hydroxide.
4. A composition as in claim 3, wherein said alkali includes a mixture of potassium and sodium.
5. A composition as in claim 2, wherein said potassium hydroxide
comprises, by weight, 0.5-2.50% of said composition.
6. A composition as in claim 3, wherein said sodium hydroxide
comprises, by weight, 0.5-2.50% of said composition.
7. A composition as in claim 1, wherein the glass transition temperature of said coating composition is in the range of approximately 0 to 10°C.
8. A composition as in claim 7, wherein the glass transition temperature
of said coating composition is in the range of approximately 3 to 8 °C.
9. A composition as in claim 1 , wherein at least one of said acrylic
polymers is a styrenated acrylic polymer.
10. A composition as in claim 1 , wherein all of said acrylic polymers are styrenated acrylic polymers.
11. A composition as in claim 1 , having a viscosity in the range of 30 to
1500 centipoise at 20°C.
12. A composition as in claim 1 , wherein said polymer mix comprises, by weight, 10-35% of said composition.
13. A composition as in claim 1, further including, by weight, 0.5-2.0%
of an emulsion of 50%> wax in water.
14. A composition as in claim 1, further including 0.1-1.0%) of a chelating agent.
15. A composition as in claim 1 , further including, by weight, 0.1-1.0%
of a surfactant.
16. A composition as in claim 1, further including an auxiliary ingredient
selected from the group consisting of: UV blocking agents, biocides, fungicides,
defoamers, fragrances, coloring agents, and combinations thereof.
17. A composition as in claim 1 including a third acrylic polymer.
18. A composition as in claim 17, wherein said first, second, and third
acrylic polymers total, by weight, approximately 15% of said composition.
19. A composition as in claim 1, further including an alcohol to decrease
the drying time of said coating.
20. A dried film prepared by evaporating water from the composition of
claim 1.
21. A dried film as in claim 20, wherein the Tg of said film is in the range
of approximately 0 to 10 ° C .
22. A coating composition for producing a water washable, protective coating, said composition comprising, by weight: 1-5% of a first acrylic polymer having a molecular weight in the range of
125,000-175,000, an acid number in the range of 80-120, and a Tg in
the range of 60-80 °C; 6-15% of a second acrylic polymer having a molecular weight in the range of 1 ,000-2,000, an acid number in the range of 180-230, and a Tg in
the range of 70-110°C;
3-10%) of a third acrylic polymer having a molecular weight in the range
of 175,000-250,000, an acid number in the range of 60-90, and a Tg in the range of20-50°C; 3-10% of a fourth acrylic polymer having a molecular weight in the range
of 5,000-10,000, an acid number in the range of 50-70, and a Tg of
less than 0°C;
water; and
an alkali in an amount sufficient to maintain the composition at a pH in the range of 7.5-9.5.
23. A composition as in claim 22, wherein said first, second, third and
fourth acrylic polymers collectively total, by weight, 10-40% of said composition.
24. A composition as in claim 22, wherein said first, second, third and
fourth acrylic polymers total, by weight, 20% of said composition.
25. A composition as in claim 22, having a viscosity in the range of 30- 1500 centipoise at 20°C.
26. A composition as in claim 22, further including, by weight, 0.5-2.0% of an emulsion of 50% wax in water.
27. A composition as in claim 22, further including 0.1-1.0% of a
chelating agent.
28. A composition as in claim 22, further including, by weight, 0.1-1.0%
of a surfactant.
29. A composition as in claim 22, further including an auxiliary ingredient
selected from the group consisting of: UV blocking agents, biocides, fungicides, defoamers, fragrances, coloring agents, and combinations thereof.
30. A composition as in claim 21 , further including an alcohol to decrease the drying time of said coating.
31. A composition as in claim 22, comprising, by weight, 1.2% of said
first acrylic polymer; 9.0% of said second acrylic polymer; 4.0%> of said third
acrylic polymer; 4.0% of said fourth acrylic polymer; 0.3% of a chelating agent; and 0.3 %> of a surfactant.
32. A dried film prepared by evaporating water from the composition of
claim 22.
33. A dried film as in claim 32, wherein the Tg of said film is in the range
of40-70°C.
34. A water washable, protective coating comprising, by weight: 125,000-175,000, an acid number in the range of 80-120, and a Tg in
the range of 60-80°C; 30-60% of a second acrylic polymer having a molecular weight in the range of 1 ,000-2,000, an acid number in the range of 180-230, and a
Tg in the range of 70-110°C;
15-50%) of a third acrylic polymer having a molecular weight in the range
of 175,000-250,000, an acid number in the range of 60-90, and a Tg in the range of20-50°C; and
15-50% of a fourth acrylic polymer having a molecular weight in the range
of 5,000-10,000, an acid number in the range of 50-70, and a Tg of
less than 0°C.
35. A coating as in claim 34, further including, by weight, l-5%> wax.
36. A composition as in claim 34, further including an auxiliary material therein selected from the group consisting of: surfactants, chelating agents, UV
blocking agents, biocides, fungicides, coloring agents, fragrances, and
combinations thereof.
37. A composition as in claim 34, further including an alcohol to decrease the drying time of said coating.
25
38. A coating composition for producing a water washable, protective
coating, said composition comprising, by weight: 10-50%) of a mix of at least two acrylic polymers, said polymers having
different molecular weights, acid numbers and glass transition
temperatures;
water; and an alkali, in an amount sufficient to maintain the composition at a pH in
the range of 7.5 to 9.5, said composition further characterized in that
the average molecular weight of said mix of at least two acrylic
polymers is in the range of 35,000 to 70,000, the average acid number of said mix is in the range of 65 to 150, and the glass transition temperature of a coating produced by the evaporation of the water
from said composition is in the range 40 to 70°C.
39. A composition as in claim 38, having a viscosity in the range of 30 to
1500 centipoise at 20°C.
40. A composition as in claim 38, wherein said polymer mix comprises,
by weight, 10-35% of said composition.
41. A coating composition for producing a water washable protective
coating, said composition comprising by weight:
10-50% of a mix of at least two acrylic polymers, a first one of said polymers having a molecular weight of no more than 2,000 and an
acid number of at least 180;
water; and an alkali, in an amount sufficient to maintain the composition at a pH in the range of 7.5 to 9.5.
42. A coating composition as in claim 41 , wherein a second one of said
at least two acrylic polymers comprises a film forming polymer, and wherein the average molecular weight of said composition is at least 35,000.
EP98944534A 1998-08-25 1998-08-26 Water washable protective coating Withdrawn EP1109852A4 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US139818 1980-04-14
US09/139,818 US6011107A (en) 1997-08-26 1998-08-25 Water washable protective coating
PCT/US1998/017681 WO1999010414A1 (en) 1997-08-26 1998-08-26 Water washable protective coating

Publications (2)

Publication Number Publication Date
EP1109852A1 true EP1109852A1 (en) 2001-06-27
EP1109852A4 EP1109852A4 (en) 2004-04-14

Family

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Country Link
EP (1) EP1109852A4 (en)
JP (1) JP2003521549A (en)
CN (1) CN1336941A (en)
CA (1) CA2341456A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2744980C (en) * 2008-12-01 2017-01-03 Basf Se Aqueous binder composition comprising oligomers
KR102266647B1 (en) * 2019-06-10 2021-06-21 주식회사 케이씨씨 Clear coat composition for refinishing automobiles

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5330788A (en) * 1992-08-10 1994-07-19 Henkel Corporation Temporary coating system
WO1998055535A1 (en) * 1997-06-06 1998-12-10 Product Sol, Llc. Methods for protecting paint on an article, composition useful therefor, and method for making the composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5330788A (en) * 1992-08-10 1994-07-19 Henkel Corporation Temporary coating system
WO1998055535A1 (en) * 1997-06-06 1998-12-10 Product Sol, Llc. Methods for protecting paint on an article, composition useful therefor, and method for making the composition

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9910414A1 *

Also Published As

Publication number Publication date
JP2003521549A (en) 2003-07-15
CN1336941A (en) 2002-02-20
EP1109852A4 (en) 2004-04-14
CA2341456A1 (en) 1999-03-04

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