CA2392515A1 - Uv curable compositions for producing decorative metallic coatings - Google Patents
Uv curable compositions for producing decorative metallic coatings Download PDFInfo
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- CA2392515A1 CA2392515A1 CA002392515A CA2392515A CA2392515A1 CA 2392515 A1 CA2392515 A1 CA 2392515A1 CA 002392515 A CA002392515 A CA 002392515A CA 2392515 A CA2392515 A CA 2392515A CA 2392515 A1 CA2392515 A1 CA 2392515A1
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- metallic composition
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
- C09D163/10—Epoxy resins modified by unsaturated compounds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1811—C10or C11-(Meth)acrylate, e.g. isodecyl (meth)acrylate, isobornyl (meth)acrylate or 2-naphthyl (meth)acrylate
Abstract
The present invention discloses an ultraviolet light curable decorative metallic composition and method for making such a composition that may be us ed to produce a decorative metallic coating on a substrate. The disclosed composition does not contain any significant amount of volatile organic solvents.
Description
UV CURABLE COMPOSITIONS FOR PRODUCING
DECORATIVE METALLIC COATINGS
TECHNICAL FIELD
The present invention relates to ultraviolet light curable compositions that may be utilized to produce a decorative metallic coating on a substrate.
BACKGROUND OF THE INVENTION
UV radiation curable paint compositions are applied to a substrate through spraying, screen printing, dipping or brushing for the protection or decoration of the substrate. In the usual application, a substrate such as metals, glass, or plastics is coated with the paint composition and then UV light is introduced to complete the curing process. The UV curable paint compositions offer many advantages over typical heat curable compositions.
Heat curable compositions require the use of organic solvents that contain a significant amount of volatile organic compounds (VOCs). These VOCs escape into the atmosphere while the heat curable composition dries. Such solvent based systems are undesirable because of the hazards and expenses associated with VOCs. The hazards include water and air pollution and the expenses include the cost of complying with strict government regulation on solvent emission levels. In contrast, UV curable compositions contain reactive monomers instead of solvents;
thus eliminating the detrimental effects of the VOCs.
The use of heat curable compositions not only raises environmental concerns but other disadvantages exist with their use as well. Heat curable compositions suffer from slow cure times which lead to decreased productivity.
These compositions require high energy for curing due to energy loss as well as the energy required to heat the substrate. Additionally, many heat curable compositions yield poor film properties that result in decreased value of the end product.
Although UV curable compositions exhibit superior properties and performance over their heat curable counterparts, UV curable compositions themselves suffer from certain disadvantages. Generally, UV compositions have high molecular weights and a substantial degree of cross linkage due to the highly reactive nature of the composition. As a result, many of these compositions suffer from low durability and resin shrinkage. With the use of many such compositions, an inordinately high amount of UV light is required to cure. New formulations that lessen these problems typically suffer from diminished abrasion, chemical, and scratch resistance as well as low thermal stability and adhesion.
An addition disadvantage of typical UV compositions is their lack of stability which results in dispersion. With some compositions, suspended solids fall out of solution after a period of one to two days. Dispersion adversely affects the gloss and clarity of the finished product. To combat this problem, new compositions have been formulated with higher viscosities which often lessen the flowability of the composition. These viscous formulations rule out spray application and provide for an unsuitably high dipping thickness.
Accordingly, there exists a need to provide environmentally safe UV
curable paint compositions which exhibit improved weatherability, corrosion resistance and workability. Additionally, there is a need to provide a method of applying the composition which furthers the goal of improved performance.
SUMMARY OF INVENTION
It is an object of the present invention to provide an improved composition that upon curing by ultraviolet light produces a decorative metallic coating.
It is another object of the present invention to provide an improved decorative metallic composition that can be applied by spraying, screen printing, dipping, and brushing.
DECORATIVE METALLIC COATINGS
TECHNICAL FIELD
The present invention relates to ultraviolet light curable compositions that may be utilized to produce a decorative metallic coating on a substrate.
BACKGROUND OF THE INVENTION
UV radiation curable paint compositions are applied to a substrate through spraying, screen printing, dipping or brushing for the protection or decoration of the substrate. In the usual application, a substrate such as metals, glass, or plastics is coated with the paint composition and then UV light is introduced to complete the curing process. The UV curable paint compositions offer many advantages over typical heat curable compositions.
Heat curable compositions require the use of organic solvents that contain a significant amount of volatile organic compounds (VOCs). These VOCs escape into the atmosphere while the heat curable composition dries. Such solvent based systems are undesirable because of the hazards and expenses associated with VOCs. The hazards include water and air pollution and the expenses include the cost of complying with strict government regulation on solvent emission levels. In contrast, UV curable compositions contain reactive monomers instead of solvents;
thus eliminating the detrimental effects of the VOCs.
The use of heat curable compositions not only raises environmental concerns but other disadvantages exist with their use as well. Heat curable compositions suffer from slow cure times which lead to decreased productivity.
These compositions require high energy for curing due to energy loss as well as the energy required to heat the substrate. Additionally, many heat curable compositions yield poor film properties that result in decreased value of the end product.
Although UV curable compositions exhibit superior properties and performance over their heat curable counterparts, UV curable compositions themselves suffer from certain disadvantages. Generally, UV compositions have high molecular weights and a substantial degree of cross linkage due to the highly reactive nature of the composition. As a result, many of these compositions suffer from low durability and resin shrinkage. With the use of many such compositions, an inordinately high amount of UV light is required to cure. New formulations that lessen these problems typically suffer from diminished abrasion, chemical, and scratch resistance as well as low thermal stability and adhesion.
An addition disadvantage of typical UV compositions is their lack of stability which results in dispersion. With some compositions, suspended solids fall out of solution after a period of one to two days. Dispersion adversely affects the gloss and clarity of the finished product. To combat this problem, new compositions have been formulated with higher viscosities which often lessen the flowability of the composition. These viscous formulations rule out spray application and provide for an unsuitably high dipping thickness.
Accordingly, there exists a need to provide environmentally safe UV
curable paint compositions which exhibit improved weatherability, corrosion resistance and workability. Additionally, there is a need to provide a method of applying the composition which furthers the goal of improved performance.
SUMMARY OF INVENTION
It is an object of the present invention to provide an improved composition that upon curing by ultraviolet light produces a decorative metallic coating.
It is another object of the present invention to provide an improved decorative metallic composition that can be applied by spraying, screen printing, dipping, and brushing.
The present invention discloses an ultraviolet light curable decorative metallic composition and method for making such a composition that may be used to produce a decorative metallic layer. The disclosed composition does not contain any significant amount of volatile organic solvents that do not become incorporated in the active layer after curing. Specifically, the decorative metallic composition contains 5 % or less volatile organic solvents by weight.
In accordance with one aspect of the invention, an ultraviolet light curable decorative metallic composition is provided. The decorative metallic composition comprises an acrylated epoxy oligomer in an amount of about 20 %
to 45 % , an isobornyl acrylate monomer in an amount of about 15 % to 40 % of the decorative metallic composition, a photoinitiator in an amount of about 4 % to of the decorative metallic composition, a flow promoting agent in an amount of 0%
to 8 %of the decorative metallic composition, and a metallic pigment in an amount of 5 % to 40 % . All percentages of the decorative metallic composition as expressed in this document refer to the weight percentage of the stated component to the total weight of the decorative metallic composition in its fluid state at standard temperature and pressure.
In accordance with yet another aspect of the invention, a method is provided for depositing a decorative metallic coating on a substrate. The method comprises a first step of applying to the substrate a decorative metallic fluid-phase composition ("decorative metallic composition"). The decorative metallic composition includes an acrylated epoxy oligomer in an amount of about 20% to 45 % , an isobornyl acrylate monomer in an amount of about 15 % to 40 % of the decorative metallic composition, a photoinitiator in an amount of about 4 % to 14 %
of the decorative metallic composition, a flow promoting agent in an amount of 0 %
to 8 % of the decorative metallic composition, and a metallic pigment in an amount of 5 % to 40 % .
The method also includes a second step of illuminating the decorative metallic composition on the substrate with an ultraviolet light to cause the decorative metallic composition to cure into the decorative metallic coating.
In accordance with one aspect of the invention, an ultraviolet light curable decorative metallic composition is provided. The decorative metallic composition comprises an acrylated epoxy oligomer in an amount of about 20 %
to 45 % , an isobornyl acrylate monomer in an amount of about 15 % to 40 % of the decorative metallic composition, a photoinitiator in an amount of about 4 % to of the decorative metallic composition, a flow promoting agent in an amount of 0%
to 8 %of the decorative metallic composition, and a metallic pigment in an amount of 5 % to 40 % . All percentages of the decorative metallic composition as expressed in this document refer to the weight percentage of the stated component to the total weight of the decorative metallic composition in its fluid state at standard temperature and pressure.
In accordance with yet another aspect of the invention, a method is provided for depositing a decorative metallic coating on a substrate. The method comprises a first step of applying to the substrate a decorative metallic fluid-phase composition ("decorative metallic composition"). The decorative metallic composition includes an acrylated epoxy oligomer in an amount of about 20% to 45 % , an isobornyl acrylate monomer in an amount of about 15 % to 40 % of the decorative metallic composition, a photoinitiator in an amount of about 4 % to 14 %
of the decorative metallic composition, a flow promoting agent in an amount of 0 %
to 8 % of the decorative metallic composition, and a metallic pigment in an amount of 5 % to 40 % .
The method also includes a second step of illuminating the decorative metallic composition on the substrate with an ultraviolet light to cause the decorative metallic composition to cure into the decorative metallic coating.
In accordance with this method, the decorative metallic composition can be selectively deposited on the substrate at specific locations where decorative metallic plating is desired. It need not be applied to the entire substrate.
BEST MODE FOR CARRYING OUT THE INVENTION
Decorative metallic Compositions Reference will now be made in detail to presently preferred compositions or embodiments and methods of the invention, which constitute the best modes of practicing the invention presently known to the inventor.
In accordance with one aspect of the invention, a presently preferred ultraviolet light curable decorative metallic composition ("decorative metallic composition") is provided. In this preferred embodiment, the decorative metallic composition includes an acrylated epoxy oligomer. The acrylated epoxy oligomer is present in an amount of about 20 % to 45 % . The acrylated epoxy oligomer is more preferably present in an amount of about 35 % to 45 % , and most preferably about 40 % . Suitable acrylated epoxy oligomers include Radcure Ebecryl 3603 (novolac epoxy acrylate diluted 20 % by weight with tripropylene glycol diacrylate), commercially available from Radcure UCB Corp.; Sartomer CN-120 (difunctional bisphenol based epoxy acrylate) and CN-124 (difunctional bisphenol based epoxy acrylate), commercially available from Sartomer Corp.; and Echo Resin THE 9310 and 9345, commercially available from Echo Resins. The preferred acrylated epoxy oligomer is Ebecryl 3603, which is a tri-functional acrylated epoxy novolac.
Combinations of these materials may also be employed herein.
The preferred decorative metallic composition also includes an isobornyl acrylate monomer in an amount of about 15 % to 40 % . The isobornyl acrylate monomer is more preferably present in an amount of about 25 % to 35 %
, and most preferably about 28 % . Suitable isobornyl acrylate monomers include Sartomer SR-423 (isobornyl methacrylate):
BEST MODE FOR CARRYING OUT THE INVENTION
Decorative metallic Compositions Reference will now be made in detail to presently preferred compositions or embodiments and methods of the invention, which constitute the best modes of practicing the invention presently known to the inventor.
In accordance with one aspect of the invention, a presently preferred ultraviolet light curable decorative metallic composition ("decorative metallic composition") is provided. In this preferred embodiment, the decorative metallic composition includes an acrylated epoxy oligomer. The acrylated epoxy oligomer is present in an amount of about 20 % to 45 % . The acrylated epoxy oligomer is more preferably present in an amount of about 35 % to 45 % , and most preferably about 40 % . Suitable acrylated epoxy oligomers include Radcure Ebecryl 3603 (novolac epoxy acrylate diluted 20 % by weight with tripropylene glycol diacrylate), commercially available from Radcure UCB Corp.; Sartomer CN-120 (difunctional bisphenol based epoxy acrylate) and CN-124 (difunctional bisphenol based epoxy acrylate), commercially available from Sartomer Corp.; and Echo Resin THE 9310 and 9345, commercially available from Echo Resins. The preferred acrylated epoxy oligomer is Ebecryl 3603, which is a tri-functional acrylated epoxy novolac.
Combinations of these materials may also be employed herein.
The preferred decorative metallic composition also includes an isobornyl acrylate monomer in an amount of about 15 % to 40 % . The isobornyl acrylate monomer is more preferably present in an amount of about 25 % to 35 %
, and most preferably about 28 % . Suitable isobornyl acrylate monomers include Sartomer SR-423 (isobornyl methacrylate):
O
I
C=O
I
I I
and SR-506 (isobornyl acrylate):
I I
O-C-C=CH2 available from Sartomer Corp.; Radcure IBOA (isobornyl acrylate), commercially available from Radcure Corp.; IBOA and IBOMA, commercially available from CPS
Chemical; and Genomer 1121, commercially available from Rahn Radiation Curing.
The preferred isobornyl acrylate monomers is Radcure IBOA, commercially available from Radcure Corp. Radcure IBOA is a high purity, low color monomer.
Combinations of these materials may also be employed herein.
This preferred decorative metallic composition also includes a photoinitiator in an amount of about 4 % to 14 % of the decorative metallic composition. The photoinitiator is more preferably present in an amount of about 8 % to 12 % , and most preferably about 10 % . Suitable photoinitiators include Irgacure 184 (1-hydroxycyclohexyl phenyl ketone); Irgacure 907 (2-methyl-1-[4-(methylthio)phenyl]-2-morpholino propan-1-one); Irgacure 369 (2-benzyl-2-N,N-dimethylamino-1-(4-morpholinophenyl)-1-butanone); Irgacure 500 (the combination of 50 % by weight 1-hydroxy cyclohexyl phenyl ketone and 50 % by weight benzophenone); Irgacure 651 (2,2-dimethoxy-2-phenyl acetophenone); Irgacure 1700 (the combination of 25 % by weight bis(2,6-dimethoxybenzoyl-2,4-,4-trimethyl pentyl phosphine oxide and 75 % by weight 2-hydroxy-2-methyl-1-phenyl-propan-1-one); Darocur 1173 (2-hydroxy-2-methyl-lphenyl-1-propane); and Darocur 4265 (the combination of 50 % by weight 2,4,6-trimethylbenzoyldiphenyl- phosphine oxide and 50 % by weight 2-hydroxy 2-methyl-1-phenyl-propan-1-one)available commercially from Ciba-Geigy Corp., Tarrytown, N.Y.; CYRACURE UVI-6974 (mixed triaryl sulfonium hexafluoroantimonate salts) and CYRACURE UVI-6990 (mixed triaryl sulfonium hexafluorophosphate salts) available commercially from Union Carbide Chemicals and Plastics Co. Inc., Danbury, Conn.; and Genocure CQ, Genocure BOK, and Genocure M.F., commercially available from Rahn Radiation Curing. The preferred photoinitiator is IRGACURE 1700 commercially available from Ciba-Geigy of Tarrytown, New York. Combinations of these materials may also be employed herein.
The composition still further includes a flow promoting agent in an amount of about 0.0 % to 8.0 % , and preferably about 6.0 % , of the topcoat composition. Suitable flow promoting agents include Genorad 17, commercially available from Rahn Radiation Curing; and Modaflow, commercially available from Monsanto Chemical Co., St. Louis, Missouri. The preferred flow promoting agent is Modaflow which is an ethyl acrylate and 2-ethylhexyl acrylate copolymer that improves the flow of the composition. Combinations of these materials may also be employed herein.
The preferred paint composition also includes a pigmented composition in an amount of about 5 % to 40 % of the decorative metallic composition. The pigmented composition is more preferably present in an amount of about 10 % to 25 % , and most preferably about 20 % . Suitable pigmented compositions includeVenus #91 pigment and Palegold #400 available from NazDar;
and A1 #200 pigment available from Silberlne. The preferred pigment used will depend on the desired color of the paint. Combinations of these materials may also be employed herein.
To illustrate, the following example sets forth a presently preferred decorative metallic composition according to this aspect of the invention.
I
C=O
I
I I
and SR-506 (isobornyl acrylate):
I I
O-C-C=CH2 available from Sartomer Corp.; Radcure IBOA (isobornyl acrylate), commercially available from Radcure Corp.; IBOA and IBOMA, commercially available from CPS
Chemical; and Genomer 1121, commercially available from Rahn Radiation Curing.
The preferred isobornyl acrylate monomers is Radcure IBOA, commercially available from Radcure Corp. Radcure IBOA is a high purity, low color monomer.
Combinations of these materials may also be employed herein.
This preferred decorative metallic composition also includes a photoinitiator in an amount of about 4 % to 14 % of the decorative metallic composition. The photoinitiator is more preferably present in an amount of about 8 % to 12 % , and most preferably about 10 % . Suitable photoinitiators include Irgacure 184 (1-hydroxycyclohexyl phenyl ketone); Irgacure 907 (2-methyl-1-[4-(methylthio)phenyl]-2-morpholino propan-1-one); Irgacure 369 (2-benzyl-2-N,N-dimethylamino-1-(4-morpholinophenyl)-1-butanone); Irgacure 500 (the combination of 50 % by weight 1-hydroxy cyclohexyl phenyl ketone and 50 % by weight benzophenone); Irgacure 651 (2,2-dimethoxy-2-phenyl acetophenone); Irgacure 1700 (the combination of 25 % by weight bis(2,6-dimethoxybenzoyl-2,4-,4-trimethyl pentyl phosphine oxide and 75 % by weight 2-hydroxy-2-methyl-1-phenyl-propan-1-one); Darocur 1173 (2-hydroxy-2-methyl-lphenyl-1-propane); and Darocur 4265 (the combination of 50 % by weight 2,4,6-trimethylbenzoyldiphenyl- phosphine oxide and 50 % by weight 2-hydroxy 2-methyl-1-phenyl-propan-1-one)available commercially from Ciba-Geigy Corp., Tarrytown, N.Y.; CYRACURE UVI-6974 (mixed triaryl sulfonium hexafluoroantimonate salts) and CYRACURE UVI-6990 (mixed triaryl sulfonium hexafluorophosphate salts) available commercially from Union Carbide Chemicals and Plastics Co. Inc., Danbury, Conn.; and Genocure CQ, Genocure BOK, and Genocure M.F., commercially available from Rahn Radiation Curing. The preferred photoinitiator is IRGACURE 1700 commercially available from Ciba-Geigy of Tarrytown, New York. Combinations of these materials may also be employed herein.
The composition still further includes a flow promoting agent in an amount of about 0.0 % to 8.0 % , and preferably about 6.0 % , of the topcoat composition. Suitable flow promoting agents include Genorad 17, commercially available from Rahn Radiation Curing; and Modaflow, commercially available from Monsanto Chemical Co., St. Louis, Missouri. The preferred flow promoting agent is Modaflow which is an ethyl acrylate and 2-ethylhexyl acrylate copolymer that improves the flow of the composition. Combinations of these materials may also be employed herein.
The preferred paint composition also includes a pigmented composition in an amount of about 5 % to 40 % of the decorative metallic composition. The pigmented composition is more preferably present in an amount of about 10 % to 25 % , and most preferably about 20 % . Suitable pigmented compositions includeVenus #91 pigment and Palegold #400 available from NazDar;
and A1 #200 pigment available from Silberlne. The preferred pigment used will depend on the desired color of the paint. Combinations of these materials may also be employed herein.
To illustrate, the following example sets forth a presently preferred decorative metallic composition according to this aspect of the invention.
Example 1 This example provides a preferred gold decorative metallic composition according to the invention. The decorative metallic composition was made from the following components:
Component Approximate Weight %
IBOA 25.5 IRGACURE 17009.1 Ebecryl 3603 34.5 Modaflow 3 .6 Venus #91 27.3 Gold Total 100.00 In this example the IBOA and Irgacure 1700 are mixed in a pan with a propeller blade mixer for 30 seconds at a speed of 500 to 1000 rpm. In the next step, the Modaflow and the Ebecryl 3603 are introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. In the final step, the Venus #91 is introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. The temperature during mixing is monitored. The mixing is temporarily suspended if the temperature exceed 100°F.
Example 2 This example provides a preferred aluminum decorative metallic composition according to the invention. The decorative metallic composition was made from the following components:
_7_ Component Approximate Weight IBOA 31.1 IRGACURE 170011.1 Ebecryl 3603 42.2 Modaflow 4.5 A1#200 11.1 Total 100.00 In this example the IBOA and Irgacure 1700 are mixed in a pan with a propeller blade mixer for 30 seconds at a speed of 500 to 1000 rpm. In the next step, the Modaflow and the Ebecryl 3603 are introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. In the final step, the Aluminum #200 is introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm.
The temperature during mixing is monitored. The mixing is temporarily suspended if the temperature exceed 100°F.
Example 3 This example provides a preferred copper decorative metallic composition according to the invention. The decorative metallic composition was made from the following components:
Component Approximate Weight IBOA 28.0 IRGACURE 1700 10.0 Ebecryl 3603 38.0 Modaflow 4.0 Palegold #400 20.0 Copper Total 100.00 _g_ In this example the IBOA and Irgacure 1700 are mixed in a pan with a propeller blade mixer for 30 seconds at a speed of 500 to 1000 rpm. In the next step, the Modaflow and the Ebecryl 3603 are introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. In the final step, the Palegold #400 is introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm.
The temperature during mixing is monitored. The mixing is temporarily suspended if the temperature exceed 100°F.
Method for Depositing an Decorative Metallic Coating on a Substrate In accordance with still another aspect of the invention, a method is provided for depositing an decorative metallic coating on a suitable substrate. The method comprises a first step of applying a decorative metallic fluid-phase composition ("decorative metallic composition") to the substrate.
The decorative metallic composition comprises an acrylated epoxy oligomer in an amount of about 20 % to 45 % , an isobornyl acrylate monomer in an amount of about 15 % to 40 % of the decorative metallic composition, a photoinitiator in an amount of about 4 % to 14 % of the decorative metallic composition, a flow promoting agent in an amount of 0 % to 8 % of the decorative metallic composition, and a metallic pigment in an amount of 5 % to 40 % . The preferred decorative metallic compositions according to this method are those described herein, for example, including the compositions described in examples 1, 2, and 3.
The decorative metallic composition may be applied to the substrate using a number of different techniques. The decorative metallic composition may be applied, for example, by direct brush application, dipping, or it may be sprayed onto the substrate surface. It also may be applied using a screen printing technique.
In such screen printing technique, a "screen" as the term is used in the screen printing industry is used to regulate the flow of liquid composition onto the substrate surface. The decorative metallic composition typically would be applied to the screen as the latter contacts the substrate. The decorative metallic composition flows through the silk screen to the substrate, whereupon it adheres to the substrate at the desired film thickness. Screen printing techniques suitable for this purpose include known techniques, but wherein the process is adjusted in ways known to persons of ordinary skill in the art to accommodate the viscosity, flowability, and other properties of the liquid-phase composition, the substrate and its surface properties, etc. Flexographic techniques, for example, using pinch rollers to contact the decorative metallic composition with a rolling substrate, also may be used.
The method includes a second step of illuminating the decorative metallic fluid-phase composition on the substrate with an ultraviolet light to cause the decorative metallic fluid-phase composition to cure into the decorative metallic coating. This illumination may be carried out in any number of ways, provided the ultraviolet light or radiation impinges upon the decorative metallic composition so that the decorative metallic composition is caused to polymerize to form the coating, layer, film, etc., and thereby cures.
Curing preferably takes place by free radical polymerization, which is initiated by an ultraviolet radiation source. The photoinitiator preferably comprises a photoinitiator, as described above.
Various ultraviolet light sources may be used, depending on the application. Preferred ultraviolet radiation sources for a number of applications include known ultraviolet lighting equipment with energy intensity settings of, for example, 125 watts, 200 watts, and 300 watts per square inch.
While embodiments of the invention have been illustrated and described, it is not intended that these embodiments illustrate and describe all possible forms of the invention. Rather, the words used in the specification are words of description rather than limitation, and it is understood that various changes may be made without departing from the spirit and scope of the invention.
Component Approximate Weight %
IBOA 25.5 IRGACURE 17009.1 Ebecryl 3603 34.5 Modaflow 3 .6 Venus #91 27.3 Gold Total 100.00 In this example the IBOA and Irgacure 1700 are mixed in a pan with a propeller blade mixer for 30 seconds at a speed of 500 to 1000 rpm. In the next step, the Modaflow and the Ebecryl 3603 are introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. In the final step, the Venus #91 is introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. The temperature during mixing is monitored. The mixing is temporarily suspended if the temperature exceed 100°F.
Example 2 This example provides a preferred aluminum decorative metallic composition according to the invention. The decorative metallic composition was made from the following components:
_7_ Component Approximate Weight IBOA 31.1 IRGACURE 170011.1 Ebecryl 3603 42.2 Modaflow 4.5 A1#200 11.1 Total 100.00 In this example the IBOA and Irgacure 1700 are mixed in a pan with a propeller blade mixer for 30 seconds at a speed of 500 to 1000 rpm. In the next step, the Modaflow and the Ebecryl 3603 are introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. In the final step, the Aluminum #200 is introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm.
The temperature during mixing is monitored. The mixing is temporarily suspended if the temperature exceed 100°F.
Example 3 This example provides a preferred copper decorative metallic composition according to the invention. The decorative metallic composition was made from the following components:
Component Approximate Weight IBOA 28.0 IRGACURE 1700 10.0 Ebecryl 3603 38.0 Modaflow 4.0 Palegold #400 20.0 Copper Total 100.00 _g_ In this example the IBOA and Irgacure 1700 are mixed in a pan with a propeller blade mixer for 30 seconds at a speed of 500 to 1000 rpm. In the next step, the Modaflow and the Ebecryl 3603 are introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm. In the final step, the Palegold #400 is introduced into the pan and mixed for 1 to 2 minutes at a speed of 2000 rpm.
The temperature during mixing is monitored. The mixing is temporarily suspended if the temperature exceed 100°F.
Method for Depositing an Decorative Metallic Coating on a Substrate In accordance with still another aspect of the invention, a method is provided for depositing an decorative metallic coating on a suitable substrate. The method comprises a first step of applying a decorative metallic fluid-phase composition ("decorative metallic composition") to the substrate.
The decorative metallic composition comprises an acrylated epoxy oligomer in an amount of about 20 % to 45 % , an isobornyl acrylate monomer in an amount of about 15 % to 40 % of the decorative metallic composition, a photoinitiator in an amount of about 4 % to 14 % of the decorative metallic composition, a flow promoting agent in an amount of 0 % to 8 % of the decorative metallic composition, and a metallic pigment in an amount of 5 % to 40 % . The preferred decorative metallic compositions according to this method are those described herein, for example, including the compositions described in examples 1, 2, and 3.
The decorative metallic composition may be applied to the substrate using a number of different techniques. The decorative metallic composition may be applied, for example, by direct brush application, dipping, or it may be sprayed onto the substrate surface. It also may be applied using a screen printing technique.
In such screen printing technique, a "screen" as the term is used in the screen printing industry is used to regulate the flow of liquid composition onto the substrate surface. The decorative metallic composition typically would be applied to the screen as the latter contacts the substrate. The decorative metallic composition flows through the silk screen to the substrate, whereupon it adheres to the substrate at the desired film thickness. Screen printing techniques suitable for this purpose include known techniques, but wherein the process is adjusted in ways known to persons of ordinary skill in the art to accommodate the viscosity, flowability, and other properties of the liquid-phase composition, the substrate and its surface properties, etc. Flexographic techniques, for example, using pinch rollers to contact the decorative metallic composition with a rolling substrate, also may be used.
The method includes a second step of illuminating the decorative metallic fluid-phase composition on the substrate with an ultraviolet light to cause the decorative metallic fluid-phase composition to cure into the decorative metallic coating. This illumination may be carried out in any number of ways, provided the ultraviolet light or radiation impinges upon the decorative metallic composition so that the decorative metallic composition is caused to polymerize to form the coating, layer, film, etc., and thereby cures.
Curing preferably takes place by free radical polymerization, which is initiated by an ultraviolet radiation source. The photoinitiator preferably comprises a photoinitiator, as described above.
Various ultraviolet light sources may be used, depending on the application. Preferred ultraviolet radiation sources for a number of applications include known ultraviolet lighting equipment with energy intensity settings of, for example, 125 watts, 200 watts, and 300 watts per square inch.
While embodiments of the invention have been illustrated and described, it is not intended that these embodiments illustrate and describe all possible forms of the invention. Rather, the words used in the specification are words of description rather than limitation, and it is understood that various changes may be made without departing from the spirit and scope of the invention.
Claims (17)
1. A photocurable decorative metallic composition comprising:
a photocurable organic mixture;
a photointiator; and a metallic pigment.
a photocurable organic mixture;
a photointiator; and a metallic pigment.
2. The photocurable decorative metallic composition of claim 1 wherein the photocurable organic mixture comprises:
an acrylated epoxy oligomer; and an isobornyl acrylate monomer.
an acrylated epoxy oligomer; and an isobornyl acrylate monomer.
3. The metallic composition of claim 2 wherein the isobornyl acrylate monomer is selected from the group consisting of isobornyl acrylate, isobornyl methacrylate, and mixtures thereof.
4. The metallic composition of claim 2 wherein the photoinitiator is selected from the group consisting of:
1-hydroxycyclohexyl phenyl ketone;
2-methyl-1-[4-(methylthio)phenyl]-2-morpholino propan-1-;
the combination of 50% 1-hydroxy cyclohexyl phenyl ketone and 50%
benzophenone;
2,2-dimethoxy-1,2-diphenylethan-1-one;
the combination of 25% bis(2,6-dimethoxybenzoyl-2,4-, 4-trimethyl pentyl phosphine oxide and 75% 2-hydroxy-2-methyl-1-phenyl-propan-1-one;
2-hydroxy-2-methyl-1-phenyl-1-propane;
the combination of 50% 2,4,6-trimethylbenzoyldiphenyl-phosphine oxide and 50% 2-hydroxy 2-methyl-1-phenyl-propan-1-one;
mixed triaryl sulfonium hexafluoroantimonate salts, mixed triaryl sulfonium hexafluorophosphate salts; and mixtures thereof.
1-hydroxycyclohexyl phenyl ketone;
2-methyl-1-[4-(methylthio)phenyl]-2-morpholino propan-1-;
the combination of 50% 1-hydroxy cyclohexyl phenyl ketone and 50%
benzophenone;
2,2-dimethoxy-1,2-diphenylethan-1-one;
the combination of 25% bis(2,6-dimethoxybenzoyl-2,4-, 4-trimethyl pentyl phosphine oxide and 75% 2-hydroxy-2-methyl-1-phenyl-propan-1-one;
2-hydroxy-2-methyl-1-phenyl-1-propane;
the combination of 50% 2,4,6-trimethylbenzoyldiphenyl-phosphine oxide and 50% 2-hydroxy 2-methyl-1-phenyl-propan-1-one;
mixed triaryl sulfonium hexafluoroantimonate salts, mixed triaryl sulfonium hexafluorophosphate salts; and mixtures thereof.
5. The metallic composition of claim 2 wherein the acrylated epoxy oligomer is selected from the group consisting of:
novolac epoxy acrylate diluted 20% by weight with tripropylene glycol diacrylate;
difunctional bisphenol based epoxy acrylate; and mixtures thereof.
novolac epoxy acrylate diluted 20% by weight with tripropylene glycol diacrylate;
difunctional bisphenol based epoxy acrylate; and mixtures thereof.
6. The photocurable decorative metallic composition of claim 2 further comprising a flow promoting agent.
7. The photocurable decorative metallic composition of claim 6 wherein:
the acrylated epoxy oligomer is about 20% to 45% of the weight of the metallic composition;
the isobornyl acrylate monomer is about 15% to 40% of the weight of the metallic composition;
the photoinitiator is about 4% to 14% of the weight of the metallic composition;
the metallic pigment is about 5% to 40% of the weight of the metallic composition; and the flow promoting agent is about 0% to 8% of the weight of the metallic composition.
the acrylated epoxy oligomer is about 20% to 45% of the weight of the metallic composition;
the isobornyl acrylate monomer is about 15% to 40% of the weight of the metallic composition;
the photoinitiator is about 4% to 14% of the weight of the metallic composition;
the metallic pigment is about 5% to 40% of the weight of the metallic composition; and the flow promoting agent is about 0% to 8% of the weight of the metallic composition.
8. The photocurable decorative metallic composition of claim 7 wherein:
the acrylated epoxy oligomer is about 35% to 45% of the weight of the metallic composition;
the isobornyl acrylate monomer is about 25% to 35% of the weight of the metallic composition;
the photoinitiator is about 8% to 12% of the weight of the metallic composition;
the metallic pigment is about 10% to 25% of the weight of the metallic composition; and the flow promoting agent is about 0% to 8% of the weight of the metallic composition.
the acrylated epoxy oligomer is about 35% to 45% of the weight of the metallic composition;
the isobornyl acrylate monomer is about 25% to 35% of the weight of the metallic composition;
the photoinitiator is about 8% to 12% of the weight of the metallic composition;
the metallic pigment is about 10% to 25% of the weight of the metallic composition; and the flow promoting agent is about 0% to 8% of the weight of the metallic composition.
9. The photocurable decorative metallic composition of claim 8 wherein:
the acrylated epoxy oligomer is about 40% of the weight of the metallic composition;
the isobornyl acrylate monomer is about 28% of the weight of the metallic composition;
the photoinitiator is about 10% of the weight of the metallic composition;
the metallic pigment is about 20% of the weight of the metallic composition; and the flow promoting agent is about 6% of the weight of the metallic composition.
the acrylated epoxy oligomer is about 40% of the weight of the metallic composition;
the isobornyl acrylate monomer is about 28% of the weight of the metallic composition;
the photoinitiator is about 10% of the weight of the metallic composition;
the metallic pigment is about 20% of the weight of the metallic composition; and the flow promoting agent is about 6% of the weight of the metallic composition.
10. A method for coating a substrate with a photocurable metallic composition, the method comprising:
applying the metallic composition to the substrate, wherein the metallic composition includes:
an acrylated epoxy oligomer in an amount of about 20% to 45% of the weight of the metallic composition;
an isobornyl acrylate monomer in an amount of about 15% to 40% of the weight of the metallic composition;
an photoinitiator in an amount of about 4% to 14% of the weight of the metallic composition;
an metallic pigment in an amount of about 5% to 40% of the weight of the metallic composition;
an flow promoting agent in an amount of about 0% to 8% of the weight of the metallic composition; and illuminating the metallic composition with UV light such that the metallic composition is caused to form the coating as it cures.
applying the metallic composition to the substrate, wherein the metallic composition includes:
an acrylated epoxy oligomer in an amount of about 20% to 45% of the weight of the metallic composition;
an isobornyl acrylate monomer in an amount of about 15% to 40% of the weight of the metallic composition;
an photoinitiator in an amount of about 4% to 14% of the weight of the metallic composition;
an metallic pigment in an amount of about 5% to 40% of the weight of the metallic composition;
an flow promoting agent in an amount of about 0% to 8% of the weight of the metallic composition; and illuminating the metallic composition with UV light such that the metallic composition is caused to form the coating as it cures.
11. The method of claim 10, wherein the method of applying the metallic composition is spraying.
12. The method of claim 10, wherein the method of applying the metallic composition is screen printing.
13. The method of claim 10, wherein the method of applying the metallic composition is dipping the substrate into the composition sufficiently to cause the composition to uniformly coat the substrate.
14. The method of claim 10, wherein the method of applying the metallic composition is brushing.
15. A method for coating a substrate with a photocurable metallic composition, the method comprising:
applying the metallic composition to the substrate, wherein the metallic composition includes:
the acrylated epoxy oligomer in an amount of about 35 % to 45 % of the weight of the metallic composition;
the isobornyl acrylate monomer in an amount of about 25 %
to 40 % of the weight of the metallic composition;
the photoinitiator in an amount of about 8 % to 12 % of the weight of the metallic composition;
the metallic pigment in an amount of about 10 % to 25 % of the weight of the metallic composition;
the flow promoting agent in an amount of about 0 % to 8 % of the weight of the metallic composition; and illuminating the metallic composition with an UV light sufficient to cause the metallic composition to be incorporated into the metallic coating by the time the composition is cured.
applying the metallic composition to the substrate, wherein the metallic composition includes:
the acrylated epoxy oligomer in an amount of about 35 % to 45 % of the weight of the metallic composition;
the isobornyl acrylate monomer in an amount of about 25 %
to 40 % of the weight of the metallic composition;
the photoinitiator in an amount of about 8 % to 12 % of the weight of the metallic composition;
the metallic pigment in an amount of about 10 % to 25 % of the weight of the metallic composition;
the flow promoting agent in an amount of about 0 % to 8 % of the weight of the metallic composition; and illuminating the metallic composition with an UV light sufficient to cause the metallic composition to be incorporated into the metallic coating by the time the composition is cured.
16. The method of claim 15, wherein:
the acrylated epoxy oligomer is about 40 % of the weight of the metallic composition;
the isobornyl acrylate monomer is about 28 % of the weight of the metallic composition;
the photoinitiator is about 10 % of the weight of the metallic composition;
the metallic pigment is about 20 % of the weight of the metallic composition; and the flow promoting agent is about 6.0 % of the weight of the metallic composition.
the acrylated epoxy oligomer is about 40 % of the weight of the metallic composition;
the isobornyl acrylate monomer is about 28 % of the weight of the metallic composition;
the photoinitiator is about 10 % of the weight of the metallic composition;
the metallic pigment is about 20 % of the weight of the metallic composition; and the flow promoting agent is about 6.0 % of the weight of the metallic composition.
17. A method of making a photocurable metallic composition comprising:
mixing an isobornyl acrylate monomer and a photoinitiator in a pan;
introducing a flow promoting agent and an acrylated epoxy oligomer into the pan;
mixing the flow promoting agent and the acrylated epoxy oligomer;
introducing a pigmented composition into the pan; and mixing the pigmented composition in the pan.
mixing an isobornyl acrylate monomer and a photoinitiator in a pan;
introducing a flow promoting agent and an acrylated epoxy oligomer into the pan;
mixing the flow promoting agent and the acrylated epoxy oligomer;
introducing a pigmented composition into the pan; and mixing the pigmented composition in the pan.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16924799P | 1999-12-06 | 1999-12-06 | |
| US60/169,247 | 1999-12-06 | ||
| PCT/US2000/042605 WO2001040387A2 (en) | 1999-12-06 | 2000-12-06 | Uv curable compositions for producing decorative metallic coatings |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2392515A1 true CA2392515A1 (en) | 2001-06-07 |
Family
ID=22614814
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002392515A Abandoned CA2392515A1 (en) | 1999-12-06 | 2000-12-06 | Uv curable compositions for producing decorative metallic coatings |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1252242A2 (en) |
| AU (1) | AU4139601A (en) |
| CA (1) | CA2392515A1 (en) |
| MX (1) | MXPA02005284A (en) |
| WO (1) | WO2001040387A2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8150441B2 (en) | 2006-11-06 | 2012-04-03 | Magnolia Broadband Inc. | Modifying a signal by controlling transmit diversity parameters |
| MX357092B (en) | 2012-02-07 | 2018-06-26 | Actega North America Inc | Uv curable metallic decorative compositions. |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4959178A (en) * | 1987-01-27 | 1990-09-25 | Advanced Products Inc. | Actinic radiation-curable conductive polymer thick film compositions and their use thereof |
| US5180757A (en) * | 1987-12-16 | 1993-01-19 | Michael Lucey | Photopolymerizable compositions used in electronics |
| US6290881B1 (en) * | 1999-04-14 | 2001-09-18 | Allied Photochemical, Inc. | Ultraviolet curable silver composition and related method |
-
2000
- 2000-12-06 EP EP00992185A patent/EP1252242A2/en not_active Withdrawn
- 2000-12-06 WO PCT/US2000/042605 patent/WO2001040387A2/en not_active Application Discontinuation
- 2000-12-06 CA CA002392515A patent/CA2392515A1/en not_active Abandoned
- 2000-12-06 AU AU41396/01A patent/AU4139601A/en not_active Abandoned
- 2000-12-06 MX MXPA02005284A patent/MXPA02005284A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1252242A2 (en) | 2002-10-30 |
| AU4139601A (en) | 2001-06-12 |
| MXPA02005284A (en) | 2003-09-22 |
| WO2001040387A3 (en) | 2001-12-13 |
| WO2001040387A2 (en) | 2001-06-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |