US20200263040A1 - Adhesion promoting compositions and method of improving fuel resistance of a coated article - Google Patents

Abstract

The present invention is directed to solventborne film-forming compositions comprising: a) a non-chlorinated, linear polyolefin polymer prepared from a reaction mixture comprising 0.5 to 5 percent by weight maleic anhydride based on the total weight of monomers in the reaction mixture; b) an aminoplast: and c) a polymer component comprising: i) an addition polymer prepared from a reaction mixture comprising coumarone; and/or ii) an alkyd resin. The present invention is also drawn to methods of improving fuel resistance of a coated article, comprising: (1) applying the solventborne film-forming composition above to a substrate to form a coated substrate; (2) applying a curable film-forming composition to at least a portion of the coated substrate formed in step (1) to form a multi-layer coated substrate; and (3) heating the multi-layer coated substrate formed in step (2) to a temperature and for a time sufficient to cure the film-forming composition.

Description

FIELD OF THE INVENTION
• The present invention relates to adhesion promoting compositions and methods of improving fuel resistance of coated articles.
BACKGROUND OF THE INVENTION
• Polymeric materials, such as thermoplastic polyolefin (TPO) and reaction injected molding urethane (RIM), are useful in many applications, such as automobile parts and accessories, containers, household appliances and other commercial items. Such polymeric materials are often used as substrates with organic coating compositions applied for aesthetic purposes or to protect them from degradation when exposed to atmospheric weathering conditions such as sunlight, moisture, heat and cold. To achieve longer lasting and more durable parts, it is important for the coatings to be firmly adhered to the surface of the article.
• Polymeric substrates made from a variety of thermoplastic and thermosetting materials have widely varying surface properties, including surface tension, roughness and flexibility, which make strong adhesion of organic coatings difficult, particularly after aging or environmental exposure of the coated polymeric materials. To facilitate adhesion of organic coatings to polymeric substrates, the substrate can be pretreated using an adhesion promoter layer or tie coat, e.g., a thin coating layer about 0.25 mils (6.35 microns) thick, or by flame or corona pretreatment. For automotive applications, it is important that the coating composition and/or adhesion promoter layer is resistant to fuel damage, i.e. maintains good adhesion of the coating to the substrate even if fuel is accidentally spilled onto the coated substrate.
• Typically, adhesion promoter layers used on TPO surfaces contain chlorinated polyolefins. Liquid adhesion promoting coating compositions containing polyolefin diols or a blend of a saturated polyhydroxylated polydiene polymer and a chlorinated polyolefin have also been developed. However, chlorinated polyolefins provide some processing limitations. For example, conventional chlorinated polyolefins typically have no curing or crosslinking sites and therefore must be used at high molecular weights to have a positive effect on coating strength.
• Additionally, while these known adhesion promoting compositions are generally acceptable for commercial applications, they tend to either have good adhesion to polymeric substrates with poor to moderate fuel resistance; or good adhesion and good fuel resistance but only with a small variety of polymeric substrate types or only at high levels of chlorinated polyolefin, resulting in high VOC. It would be desirable to provide compositions useful as adhesion promoters and service primers for automotive topcoats on plastic substrates, further demonstrating improved fuel resistance, in order to meet the new demands in automotive manufacturing such as elimination of primers.
SUMMARY OF THE INVENTION
• The present invention is directed to solventborne film-forming compositions comprising:
• • a) a non-chlorinated, linear polyolefin polymer prepared from a reaction mixture comprising 0.5 to 5 percent by weight maleic anhydride based on the total weight of monomers in the reaction mixture; and
  • b) an aminoplast: and
  • c) a polymer component comprising:
    • i) an addition polymer prepared from a reaction mixture comprising coumarone; and/or
    • ii) an alkyd resin. The compositions are useful as adhesion promoters.
• The present invention is also drawn to methods of improving fuel resistance of a coated article, comprising:
• • (1) applying the solventborne film-forming composition described herein to at least a portion of a substrate to form a coated substrate;
  • (2) applying a curable film-forming composition to at least a portion of the coated substrate formed in step (1) to form a multi-layer coated substrate; and
  • (3) heating the multi-layer coated substrate formed in step (2) to a temperature and for a time sufficient to cure the film-forming composition.
DETAILED DESCRIPTION OF THE INVENTION
• Other than in any operating examples, or where otherwise indicated, all numbers expressing quantities of ingredients, reaction conditions and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.
• Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements.
• Also, it should be understood that any numerical range recited herein is intended to include all sub-ranges subsumed therein. For example, a range of “1 to 10” is intended to include all sub-ranges between (and including) the recited minimum value of 1 and the recited maximum value of 10, that is, having a minimum value equal to or greater than 1 and a maximum value of equal to or less than 10.
• As used in this specification and the appended claims, the articles “a,” “an,” and “the” include plural referents unless expressly and unequivocally limited to one referent.
• The term “curable”, as used for example in connection with a curable composition, means that the indicated composition is polymerizable or cross linkable through functional groups, e.g., by means that include, but are not limited to, thermal (including ambient cure) and/or catalytic exposure.
• The term “cure”, “cured” or similar terms, as used in connection with a cured or curable composition, means that at least a portion of the polymerizable and/or crosslinkable components that form the curable composition is polymerized and/or crosslinked. Additionally, curing of a polymerizable composition refers to subjecting said composition to curing conditions such as but not limited to thermal curing, leading to the reaction of the reactive functional groups of the composition, and resulting in polymerization and formation of a polymerizate. When a polymerizable composition is subjected to curing conditions, following polymerization and after reaction of most of the reactive end groups occurs, the rate of reaction of the remaining unreacted reactive end groups becomes progressively slower. The polymerizable composition can be subjected to curing conditions until it is at least partially cured. The term “at least partially cured” means subjecting the polymerizable composition to curing conditions, wherein reaction of at least a portion, such as at least 10 percent, or at least 20 percent, of the reactive groups of the composition occurs, to form a polymerizate. The polymerizable composition can also be subjected to curing conditions such that a substantially complete cure is attained (such as at least 70 percent, or at least 80 percent, or at least 90 percent up to 100 percent, of the reactive groups react) and wherein further curing results in no significant further improvement in polymer properties, such as hardness.
• The various embodiments and examples of the present invention as presented herein are each understood to be non-limiting with respect to the scope of the invention.
• The solventborne film-forming composition of the present invention comprises a) a non-chlorinated, linear polyolefin polymer that may be prepared from a reaction mixture comprising 0.5 to 5 percent by weight maleic anhydride, based on the total weight of monomers in the reaction mixture. The reaction mixture used to prepare the linear polyolefin polymer a) may further comprise ethylene and/or propylene. Note that the phrase “and/or” when used in a list is meant to encompass alternative embodiments including each individual component in the list as well as any combination of components. For example, the list “A, B, and/or C” is meant to encompass seven separate embodiments that include A, or B, or C, or A+B, or A+C, or B+C, or A+B+C. The polyolefin polymers may comprise polyethylene, polypropylene, polymethylpentene, polybutene-1, polyisobutylene, and the like. The polyolefin may also be a copolymer of different olefinic monomers with other optional ethylenically unsaturated monomers. The linear polyolefin polymers often comprise polyethylene, or more often polypropylene, prepared from a reaction mixture comprising at least 0.5 percent by weight, or at least 1 percent by weight, or at least 2 percent by weight, and up to 5 percent by weight, such as up to 4 percent by weight, or up to 3 percent by weight maleic anhydride, based on the total weight of the linear polyolefin. Examples include the linear polyolefins TOYO-TAC, available from TOYOBO CO., LTD.
• The linear polyolefin polymers may be prepared so as to have (i) functional groups comprising ester and/or urethane groups and (ii) reactive groups comprising hydroxyl, epoxy, and/or siloxane groups. The reactive groups on these polyolefins may then be further reacted with a polyfunctional material, a lactone, or a lactide to yield a non-chlorinated, reactive polyolefin having (i) functional groups comprising ester and/or urethane groups and (ii) reactive groups comprising hydroxyl, epoxy, and/or siloxane groups.
• Examples of polyfunctional materials include diepoxides or higher polyepoxides. Use of a diepoxide as a difunctional material allows for bridging between polyolefins that contain acid functional groups. Other polyfunctional materials are epoxy functional alkoxysilanes such as SILQUEST® A-187, commercially available from Momentive Performance Materials; and isocyanate functional alkoxysilanes, such as SILQUEST® A-link 35, an isocyanatopropyl trimethoxy silane, and SILQUEST® A-link 25, an isocyanatopropyl triethoxy silane, both commercially available from Momentive Performance Materials.
• In certain examples of the present invention, the linear polyolefin polymer is further reacted with a polyepoxide and a monohydric alcohol. Examples of suitable monohydric alcohols include n-propanol, isopropanol, n-butanol, and/or isobutanol.
• In other examples of the present invention, the reaction mixture used to prepare the linear polyolefin polymer a) further comprises an ethylenically unsaturated monomer comprising at least one (meth)acrylic monomer, including any of those known in the art. The term “(meth)acrylate” is meant to encompass acrylate and/or methacrylate molecular structures where they exist. Examples of suitable polyolefin polymers prepared in this manner are commercially available as AUROREN, from Nippon Paper.
• Each of the linear polyolefin polymers described above may be used individually or in any combination with each other in the solventborne film-forming composition.
• The linear polyolefin polymer a) may be present in the solventborne film-forming composition in an amount of at least 5 percent by weight, or at least 10 percent by weight, or at least 15 percent by weight, and up to 40 percent by weight, such as up to 30 percent by weight, or up to 20 percent by weight, based on the total weight of resin solids in the film-forming composition.
• In certain examples of the present invention, the linear polyolefin polymer a) may be dispersed in an organic medium with a polyepoxide and a monohydric alcohol. Suitable organic media include xylene, AROMATIC 100 (CAS No. 64742-95-6, a blend of C_9-10 dialkyl- and trialkylbenzenes, available from ExxonMobil), cyclohexane, and butyl acetate. The polyepoxide may be a di- or higher polyepoxide; for example, a diepoxide, such as EPONEX 1510, commercially available from Hexion, can be used. Examples of suitable monohydric alcohols include any of those disclosed above. In this example, the polyepoxide may be present in the solventborne film-forming composition in an amount of at least 0.01 percent by weight, or at least 0.10 percent by weight, or at least 0.50 percent by weight, and up to 10.00 percent by weight, such as up to 5.00 percent by weight, or up to 1.00 percent by weight, based on the total weight of resin solids in the film-forming composition. The monohydric alcohol may be present in the solventborne film-forming composition in an amount of at least 0.10 percent by weight, or at least 1.00 percent by weight, or at least 5.00 percent by weight, and up to 20.00 percent by weight, such as up to 16.00 percent by weight, or up to 8.00 percent by weight, based on the total weight of resin solids in the film-forming composition.
• The solventborne film-forming composition of the present invention further comprises b) an aminoplast. Useful aminoplast resins are addition products of formaldehyde with an amino- or amido-group carrying substance. Condensation products obtained from the reaction of alcohols and formaldehyde with melamine, urea or benzoguanamine are most common. While the aldehyde employed is most often formaldehyde, other similar condensation products can be made from other aldehydes, such as acetaldehyde, crotonaldehyde, acrolein, benzaldehyde, furfural, glyoxal and the like.
• The aminoplast resins often contain methylol or similar alkylol groups, and in most instances at least a portion of these alkylol groups are etherified by reaction with an alcohol. Any monohydric alcohol can be employed for this purpose, including methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, as well as benzyl alcohol and other aromatic alcohols, cyclic alcohols such as cyclohexanol, monoethers of glycols, and halogen-substituted or other substituted alcohols such as 3-chloropropanol and butoxyethanol. Many aminoplast resins are partially alkylated with methanol or butanol. Carbamoyl triazines of the formula C₃N₃(NHCOXR)₃ where X is nitrogen, oxygen or carbon and R is a lower alkyl group having from one to twelve carbon atoms or mixtures of lower alkyl groups, such as methyl, ethyl, propyl, butyl, n-octyl, and 2-ethylhexyl, are also suitable. Such compounds and their preparation are described in detail in U.S. Pat. No. 5,084,541 (column 2, line 50 through column 7, line 63) incorporated by reference in pertinent part herein.
• Imino groups and amino groups on an aminoplast resin arise from the incomplete reaction of the aldehyde with the amine. Aminoplast resins are characterized as low-imino if the imino content is less than about 10%; that is, if less than about 10% of the functional groups on the resin consist of imino or amino groups as determined by NMR analysis. Commonly, low-imino aminoplast resins contain less than 5% imino content. On the other hand, if the imino content of an aminoplast resin is greater than about 10%, it can be characterized as high-imino. More commonly, the imino content of a high imino resin is 15% or higher. Commercial high imino melamine resins, for example, are available with up to about 35% imino content. Typically the aminoplast is at least partially alkylated and 10 to 35 percent, usually 15 to 35 percent, of functional groups on the aminoplast comprise imino groups. A particularly useful aminoplast is CYMEL 1158, available from Allnex.
• The aminoplast b) may be present in the solventborne film-forming composition in an amount of at least 5 percent by weight, or at least 7 percent by weight, or at least 10 percent by weight, and up to 20 percent by weight, such as up to 17 percent by weight, or up to 15 percent by weight, based on the total weight of resin solids in the film-forming composition.
• The solventborne film-forming composition of the present invention further comprises c) a polymer component comprising i) an addition polymer prepared from a reaction mixture comprising coumarone; and/or ii) an alkyd resin. The addition polymer i) is usually prepared from a reaction mixture comprising coumarone and indene, and often additionally styrene. Such addition polymers are commercially available from Nitto Chemical as Coumarone V-120S and from Neville Chemical CO. as CUMAR 130. Suitable alkyd resins may be prepared in a known manner by condensation of polyhydric alcohols and polycarboxylic acids including fatty acids. Suitable polyhydric alcohols include, but are not limited to, ethylene glycol, propylene glycol, butylene glycol, 1,6-hexylene glycol, neopentyl glycol, diethylene glycol, glycerol, trimethylol propane, and pentaerythritol. Suitable polycarboxylic acids include, but are not limited to, succinic acid, adipic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, phthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, and trimellitic acid, as well as fatty acids, for example, those derived from linseed oil, soya bean oil, tall oil, dehydrated castor oil, or tung oil. Besides the polycarboxylic acids mentioned above, functional equivalents of the acids such as anhydrides where they exist or lower alkyl esters of the acids such as the methyl esters may be used. A particularly suitable alkyd resin is illustrated in the Examples below. Often, both i) and ii) are present in the polymer component c). The weight ratio of the linear polyolefin polymer a) to the polymer component c) in the curable film-forming composition may range from 5:95 to 40:60.
• Often the solventborne film-forming composition of the present invention further comprises a hydroxyl functional (meth)acrylic polymer and/or a hydroxyl functional polyester polymer. By “polymer” is meant a polymer including homopolymers and copolymers, and oligomers. Useful hydroxyl functional ethylenically unsaturated monomers used to prepare the (meth)acrylic polymer include hydroxyalkyl (meth)acrylates, typically having 2 to 4 carbon atoms in the hydroxyalkyl group, such as hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, hydroxy functional adducts of caprolactone and hydroxyalkyl (meth)acrylates, as well as the beta-hydroxy ester functional monomers described below.
• Beta-hydroxy ester functional monomers can be prepared from ethylenically unsaturated, epoxy functional monomers and carboxylic acids having from about 13 to about 20 carbon atoms, or from ethylenically unsaturated acid functional monomers and epoxy compounds containing at least 5 carbon atoms which are not polymerizable with the ethylenically unsaturated acid functional monomer.
• Useful ethylenically unsaturated, epoxy functional monomers used to prepare the beta-hydroxy ester functional monomers include, but are not limited to, glycidyl (meth)acrylate, allyl glycidyl ether, methallyl glycidyl ether, 1:1 (molar) adducts of ethylenically unsaturated monoisocyanates with hydroxy functional monoepoxides such as glycidol, and glycidyl esters of polymerizable polycarboxylic acids such as maleic acid. Glycidyl (meth)acrylate is preferred. Examples of carboxylic acids include, but are not limited to, saturated monocarboxylic acids such as isostearic acid and aromatic unsaturated carboxylic acids.
• Useful ethylenically unsaturated acid functional monomers used to prepare the beta-hydroxy ester functional monomers include monocarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid; dicarboxylic acids such as itaconic acid, maleic acid and fumaric acid; and monoesters of dicarboxylic acids such as monobutyl maleate and monobutyl itaconate. These acid functional monomers may also be used in the reaction mixture to prepare the first film-forming polymer, providing acid functional reactive groups thereto. The ethylenically unsaturated acid functional monomer and epoxy compound are typically reacted in a 1:1 equivalent ratio. The epoxy compound does not contain ethylenic unsaturation that would participate in free radical-initiated polymerization with the unsaturated acid functional monomer. Useful epoxy compounds include 1,2-pentene oxide, styrene oxide and glycidyl esters or ethers, usually containing from 7 to 30 carbon atoms, such as butyl glycidyl ether, octyl glycidyl ether, phenyl glycidyl ether and para-(tertiary butyl) phenyl glycidyl ether. Commonly used glycidyl esters include those of the structure:
• 
• where R is a hydrocarbon radical containing from about 4 to about 26 carbon atoms. Usually, R is a branched hydrocarbon group having from about 5 to about 10 carbon atoms, such as neopentyl, neoheptanyl or neodecanyl. Suitable glycidyl esters of carboxylic acids include CARDURA E and glycidyl esters of VERSATIC ACID 911 and, each of which is commercially available from Shell Chemical Co.
• One or more other polymerizable ethylenically unsaturated monomers may be included in the reaction mixture that may be used to prepare the hydroxyl functional (meth)acrylic polymer. Useful alkyl esters of acrylic acid or methacrylic acid include aliphatic alkyl esters containing from 1 to 30, and preferably 4 to 18 carbon atoms in the alkyl group. Non-limiting examples include methyl (meth)acrylate, ethyl (meth)acrylate, and butyl (meth)acrylate. Suitable other copolymerizable ethylenically unsaturated monomers include vinyl aromatic compounds such as styrene and vinyl toluene; nitriles such as acrylonitrile and methacrylonitrile; vinyl and vinylidene halides such as vinyl chloride and vinylidene fluoride and vinyl esters such as vinyl acetate.
• A particularly suitable hydroxyl functional (meth)acrylic polymer may be prepared as demonstrated in the Examples below. The hydroxyl functional (meth)acrylic polymer may be prepared using known addition polymerization techniques, such as organic solution polymerization techniques, in particular from the afore-mentioned reaction mixtures.
• Hydroxyl functional polyester polymers may also or alternatively be used. Such polymers may be prepared in a known manner by condensation of polyhydric alcohols and polycarboxylic acids. Suitable polyhydric alcohols include, but are not limited to, ethylene glycol, propylene glycol, butylene glycol, 1,6-hexylene glycol, neopentyl glycol, diethylene glycol, glycerol, trimethylol propane, and pentaerythritol. Suitable polycarboxylic acids include, but are not limited to, succinic acid, adipic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, phthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, and trimellitic acid. Besides the polycarboxylic acids mentioned above, functional equivalents of the acids such as anhydrides where they exist or lower alkyl esters of the acids such as the methyl esters may be used. The polyhydric alcohol is used in stoichiometric excess relative to the polycarboxylic acid to ensure hydroxyl fucnt groups on the resultant polyester polymer.
• When used, the hydroxyl functional (meth)acrylic and/or polyester polymer is present in the solventborne film-forming composition in an amount of at least 5 percent by weight, or at least 8 percent by weight, or at least 11 percent by weight, and up to 16 percent by weight, such as up to 20 percent by weight, or up to 23 percent by weight, based on the total weight of resin solids in the film-forming composition.
• The solventborne film-forming compositions of the present invention may be curable when the hydroxyl functional (meth)acrylic and/or polyester polymer is present and/or when the polyolefin polymer a) contains reactive functional groups that may react with the aminoplast. Curing may be desirable when the composition is used as a service primer to prevent damage to the resulting coating during subsequent shipping. However, it is not necessary to cure the composition (i.e., subject it to its own cure regimen) when it is used as a coating immediately prior to application of any subsequent coating layers. Curing may occur when the subsequently applied layers are subjected to curing conditions. The film-forming compositions may further contain a catalyst to facilitate any desired cure. Typical catalysts include phenyl acid phosphate and sulfonic acid functional catalysts such as dodecylbenzene sulfonic acid (DDBSA) and the like. Alternatively, the film-forming compositions may be essentially free of a catalyst. As used throughout this specification, including the claims, by “essentially free” is meant that a compound is not intentionally present in the composition; and if a compound is present in the composition, it is present incidentally in an amount less than 0.1 percent by weight, usually less than trace amounts.
• The solventborne film-forming compositions of the present invention can also include a colorant. As used herein, the term “colorant” means any substance that imparts color and/or other opacity and/or other visual effect to the composition. The colorant can be added to the coating in any suitable form, such as discrete particles, dispersions, solutions and/or flakes. A single colorant or a mixture of two or more colorants can be used in the coatings of the present invention.
• Example colorants include pigments, dyes and tints, such as those used in the paint industry and/or listed in the Dry Color Manufacturers Association (DCMA), as well as special effect compositions. A colorant may include, for example, a finely divided solid powder that is insoluble but wettable under the conditions of use. A colorant can be organic or inorganic and can be agglomerated or non-agglomerated. Colorants can be incorporated into the coatings by grinding or simple mixing. Colorants can be incorporated by grinding into the coating by use of a grind vehicle, such as an acrylic grind vehicle, the use of which will be familiar to one skilled in the art.
• Example pigments and/or pigment compositions include, but are not limited to, carbazole dioxazine crude pigment, azo, monoazo, disazo, naphthol AS, salt type (lakes), benzimidazolone, condensation, metal complex, isoindolinone, isoindoline and polycyclic phthalocyanine, quinacridone, perylene, perinone, diketopyrrolo pyrrole, thioindigo, anthraquinone, indanthrone, anthrapyrimidine, flavanthrone, pyranthrone, anthanthrone, dioxazine, triarylcarbonium, quinophthalone pigments, diketo pyrrolo pyrrole red (“DPPBO red”), titanium dioxide, carbon black and mixtures thereof. The terms “pigment” and “colored filler” can be used interchangeably.
• Example dyes include, but are not limited to, those that are solvent and/or aqueous based such as acid dyes, azoic dyes, basic dyes, direct dyes, disperse dyes, reactive dyes, solvent dyes, sulfur dyes, mordant dyes, for example, bismuth vanadate, anthraquinone, perylene, aluminum, quinacridone, thiazole, thiazine, azo, indigoid, nitro, nitroso, oxazine, phthalocyanine, quinoline, stilbene, and triphenyl methane.
• Example tints include, but are not limited to, pigments dispersed in water-based or water miscible carriers such as AQUA-CHEM 896 commercially available from Degussa, Inc., CHARISMA COLORANTS and MAXITONER INDUSTRIAL COLORANTS commercially available from Accurate Dispersions division of Eastman Chemical, Inc.
• In particular examples of the present invention, the solventborne film-forming composition further comprises a pigment colorant such as carbon black and/or TiO₂. In general, the colorant can be present in the coating composition in any amount sufficient to impart the desired property, visual and/or color effect. The colorant may comprise from 1 to 90 weight percent of the present compositions, such as from 3 to 40 weight percent or 5 to 35 weight percent, with weight percent based on the total weight of the compositions.
• The solventborne film-forming compositions of the present invention are particularly useful as adhesion promoters for subsequently applied coating compositions on industrial substrates. In accordance with the present invention, the compositions of the present invention may be used in a method of improving fuel resistance of a coated article, such as a vehicular component. By “improving fuel resistance” is meant fuel resistance of a coated article increases when subjected to the fuel resistance test as described in footnote 22 of Table 5 below. Coated articles demonstrate improved fuel resistance when coated with the compositions of the present invention using the method of the present invention, compared to articles coated with similar compositions that do not contain an aminoplast. The method comprises: (1) applying a first film-forming composition to at least a portion of a substrate to form a coated substrate, wherein the first film-forming composition comprises any of the solventborne film-forming compositions described above; (2) applying a second, curable film-forming composition to at least a portion of the coated substrate formed in step (1) to form a multi-layer coated substrate; and (3) heating the multi-layer coated substrate formed in step (2) to a temperature and for a time sufficient to cure the second, curable film-forming composition.
• The method of the present invention is particularly useful for elastomeric, plastic, or composite substrates such as those that are found on motor vehicles and used as vehicle components such as wheels, bumpers, fenders, hoods, doors, panels, etc. These vehicle parts may be formed from any of the common thermoplastic or thermosetting synthetic materials, including thermoplastic olefins such as polyethylene and polypropylene, thermoplastic urethane, polycarbonate, thermosetting sheet molding compound, reaction-injection molding compound, acrylonitrile-based materials, nylon, and the like. By “composite” is meant any substrate comprising a resinous matrix such as one or more of polypropylene, polybutylene terephthalate, polystyrene, polyaniline, polypyrrole, polyepoxide, poly(methyl methacrylate), polyurethane, and polycarbonate, reinforced with fibers typically oriented as strands, multi-ply yarns, woven sheets, or braids, and comprising at least one of stainless steel fibers, copper fibers, nickel fibers, silver fibers, aluminum fibers, glass fibers, and carbon fibers. The film-forming composition is applied to at least one surface of the substrate. A substrate may have one continuous surface, or two or more surfaces such as two opposing surfaces.
• The compositions may be applied to the substrate by one or more of a number of methods including spraying, dipping/immersion, brushing, or flow coating, but they are most often applied by spraying. The usual spray techniques and equipment for air spraying and electrostatic spraying and either manual or automatic methods can be used. The coating layer typically has a dry film thickness of 0.1-1 mils (2.5-25.4 microns), often 0.2-0.4 mils (5-10 microns).
• The film-forming compositions can be applied directly to the surface of a substrate to form a coated substrate or onto or under a primer coat or other coating as an adhesion promoter. They are also useful as service primers; i.e., a primer applied to an automotive body part that is sold to an automotive refinish/repair shop for subsequent painting.
• Multiple coating layers such as a colored base coat, a monocoat that may or may not be colored, and/or a clear coat may be applied to the coated substrate as a second, curable film-forming composition after application of the solventborne film-forming composition of the present invention. Thus these layers may comprise multiple, different coatings serving different purposes.
• After applying the second, curable film-forming composition on the coated substrate to form a multi-layer coated substrate, the multi-layer coated substrate can be heated to a temperature and for a time sufficient to cure at least the second film-forming composition; for example, by allowing it to stand at ambient temperature, or a combination of ambient temperature cure and baking, or by baking alone. Ambient temperature usually ranges from 60 to 90° F. (15.6 to 32.2° C.), such as a typical room temperature, 72° F. (22.2° C.). The composition of the present invention may be cured at ambient temperature typically in a period ranging from about 24 hours to about 36 hours. If ambient temperature and baking are utilized in combination, the composition is often allowed to stand (“flash”) for a period of from about 2 minutes to about 120 minutes at a temperature ranging from ambient to 175° F. (79.4° C.), followed by baking at a temperature up to about 275° F. (135° C.), usually 180° F. (82° C.) or 250° F. (176° C.) for a period of time ranging from about 20 minutes to about 1.5 hour. A heated cure of the film-forming composition of the present invention is particularly useful when it is used as a service primer, although the composition does not need to cure; an ambient flash is often sufficient. For plastic substrates that are heat-sensitive and may deform at high temperatures, the curable film-forming compositions may be curable at temperatures from ambient to 90° C., such as from ambient to 80° C.
• After application of the second curable film-forming composition to the coated substrate and upon curing, the coated article demonstrates fuel resistance, measured as demonstrated in the Examples below.
• The methods of the present invention are particularly suitable for the improving fuel resistance on a component of a vehicle. Such vehicles may include landcraft such as cars, trucks, sport utility vehicles, motorcycles; watercraft such as boats, ships and submarines; aircraft such as airplanes and helicopters; construction vehicles; and military vehicles, for example tanks and Humvees.
• The methods of the present invention are also suitable for improving fuel resistance on a component of an autonomous vehicle. Many vehicles in use today, including autonomous vehicles, utilize transmitters and sensors to send and receive signals for various purposes. It is vital for the continued accurate and safe operation of such vehicles that these signals, which are typically electromagnetic radiation in the form of radio waves, do not get impeded in any way. Coated substrates covering the transmitters and sensors must allow for transmission of the signals therethrough. Improving fuel resistance by using the methods of the present invention is particularly beneficial.
• Each of the embodiments and characteristics described above, and combinations thereof, may be said to be encompassed by the present invention. For example, the present invention is thus drawn to the following nonlimiting aspects:
• 1. A solventborne film-forming composition comprising:
  a) a non-chlorinated, linear polyolefin polymer prepared from a reaction mixture comprising 0.5 to 5 percent by weight maleic anhydride based on the total weight of monomers in the reaction mixture;
  b) an aminoplast: and
  c) a polymer component comprising:
• • i) an addition polymer prepared from a reaction mixture comprising coumarone; and/or
  • ii) an alkyd resin.
    2. The composition according to aspect 1 wherein the linear polyolefin polymer a) is dispersed in an organic medium with a polyepoxide and a monohydric alcohol.
    3. The composition according to aspect 2 wherein the monohydric alcohol comprises n-propanol, isopropanol, n-butanol, and/or isobutanol.
    4. The composition according to any of aspects 1 to 3 wherein the linear polyolefin polymer a) is further reacted with a polyepoxide and a monohydric alcohol.
    5. The composition according to aspect 4 wherein the monohydric alcohol comprises n-propanol, isopropanol, n-butanol, and/or isobutanol.
    6. The composition according to any of aspects 1 to 5 wherein the reaction mixture used to prepare the linear polyolefin polymer a) further comprises an ethylenically unsaturated monomer comprising at least one (meth)acrylic monomer.
    7. The composition according to any of aspects 1 to 6 wherein the aminoplast is at least partially alkylated and wherein 10 to 35 percent of functional groups on the aminoplast comprise imino groups.
    8. The composition according to any of aspects 1 to 7 wherein the polymer component c) comprises an addition polymer prepared from a reaction mixture comprising coumarone, indene, and styrene.
    9. The composition according to any of aspects 1 to 8 wherein the polymer component c) comprises i) an addition polymer prepared from a reaction mixture comprising coumarone, indene, and styrene; and ii) an alkyd resin.
    10. The composition according to any of aspects 1 to 9, further comprising a colorant such as carbon black and/or TiO₂.
    11. The composition according to any of aspects 1 to 10, further comprising a hydroxyl functional (meth)acrylic polymer and/or a hydroxyl functional polyester polymer.
    12. A method of improving fuel resistance of a coated article, comprising:
    (1) applying a first film-forming composition to at least a portion of a substrate to form a coated substrate, wherein the first film-forming composition comprises the composition according to any of aspects 1 to 11;
    (2) applying a second, curable film-forming composition to at least a portion of the coated substrate formed in step (1) to form a multi-layer coated substrate; and
    (3) heating the multi-layer coated substrate formed in step (2) to a temperature and for a time sufficient to cure the second, curable film-forming composition; wherein the substrate comprises an elastomeric, plastic, or composite material.
    13. The method according to aspect 12 wherein the multi-layer coated substrate is heated to a temperature up to 135° C. in step (3).
• The following examples are intended to illustrate various embodiments of the invention, and should not be construed as limiting the invention in any way.
EXAMPLES
• The following working examples are intended to further describe the invention. It is understood that the invention described in this specification is not necessarily limited to the examples described in this section. Note that for all measurements, the IR spectrometer used was a ThermoScientific Nicolet iS5 FT-IR. Acid number was determined via titration using a Metrohm 888 Titrando and a homogeneous sample solution of tetrahydrofuran (THF) with methanolic potassium hydroxide solution (0.1 N).
Example A: Preparation of Alkyd Resin Solution
• An Alkyd resin solution was prepared from the following charges:

• 	Ingredients	Parts by weight (g)

  Charge #1

  	NOURACID ® SE45 1	1126.2
  	Crotonic acid 2	299.2
  	Pentaerythritol 3	502.8
  	Phthalic anhydride 4	422.4
  	DBTO 5	4.18

  Charge #2

  Xylene

  46.2

  Charge #3

  	Xylene	968.9
  	1 NOURACID SE 45 is soybean oil fatty acid and commercially available from Oleon.
  	2 Crotonic acid is commercially available from Clariant Corporation.
  	3 Pentaerythritol is commercially available from Clariant Corporation.
  	4 Phthalic anhydride is commercially available from BASF.
  	5 DBTO is dibutyl tin oxide and commercially available from Arkema Inc.

• Charge 1 was added to a 5 L 4-necked flask equipped with a motor driven stainless steel stir blade, glycol recovery column, a water-cooled condenser, and a heating mantle with a thermometer connected through a temperature feedback control. The reactor contents were heated to 215° C. and water removed until the acid value was 28˜30 mg KOH/g. Then, the glycol recovery column was replaced with a Dean-Stark trap filled with xylene and charge 2 was added into reaction vessel. Water was azeotropically removed until the acid value was less than 10.0 mg KOH/g. The resulting alkyd resin was diluted with charge 3 to afford a solution with solid weight percent of 70% measured for one hour at 110° C., an acid value of 4 to 9 mg KOH/g, and a Gardner viscosity of E to G.
Example B: Preparation of Alkyd Acrylic Resin in Xylene Solution
• An Alkyd acrylic resin in xylene solution was prepared from the following charges:

• 	Ingredients	Parts by weight

  Charge #1

  	Xylene	50.82
  	T-Butyl perbenzoate 1	17.64

  Charge #2

  	Example A (Alkyd resin solution)	2736.09
  	Styrene	845.67
  	Methyl methacrylate	423.99
  	2-Ethylhexyl acrylate	139.23
  	Acrylonitrile	157.29

  Charge #3

  Xylene

  1170.12

  Charge #4

  	Xylene	273.21
  	T-Butyl perbenzoate	9.03

  Charge #5

  Xylene

  1095.0

  Charge #6

  	Xylene	295.0
  	1 T-Butyl perbenzoate is commercially available from Akzo Nobel Chemicals.

• A 12 liter, 4-necked flask equipped with a motor driven stainless steel stir blade, additional funnel, thermocouple, condenser, and a nitrogen blanket was charged with charge 1, 2, and 3. The reactor contents were heated to 125° C. slowly. External reactor cooling was applied when the reactor contents temperature reached 110° C. to control the resulting exotherm to less than 130° C. The reactor contents were stirred for one hours at 124˜127° C. Then charge 4 was added over 180 minutes, the additional funnel rinsed with charge 5 and the reactor contents stirred for another 90 minutes. Then the reactor contents were cooled to 115° C. and 14 inches of vacuum was applied to distill 1482 g solvent. Charge 5 and 6 were added to the reactor to afford a product with 55.8 weight percent solid content (measured for one hour at 110° C.), an acid value of 2 to 5 KOH/g, a Gardner viscosity of U to W, and free acrylonitrile content of less than 50 ppm.
Example C: Preparation of Alkyd Acrylic Resin in Aromatic 100 Solution
• An Alkyd acrylic resin in Aromatic 100 solution was prepared from the following charges:

• 	Ingredients	Parts by weight

  Charge #1

  	Example B (Alkyd Acrylic	2940.0
  	resin in xylene solution)

  Charge #2

  	Aromatic 100	1309.9

• Charge 1 was added to a 5 L 4-necked flask equipped with a motor driven stainless steel stir blade, a condenser with distillation adaptors, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 145° C. and vacuum was applied to distill 1286 g solvent. When distillation was completed, the vacuum and heat were off. Charge 2 was added through additional funnel over 20 minutes to afford a product with 56.11 weight percent solid content (measured for one hour at 110° C.), and a Gardner viscosity of Z.
Example D: Preparation of Polyolefin Solution
• A polyolefin solution was prepared from the following charges:

• 	Ingredients	Parts by weight (g)

  Charge #1

  AROMATIC 100

  2313.70

  Charge #2

  	EPONEX 15101	3.08
  	AROMATIC 100	24.95

  Charge #3

  TOYOBO PMA-KE2

  496.92

  Charge #4

  Cyclohexane

  696.82

  Charge #5

  	Cyclohexane	226.30
  	Isopropanol	84.61
  	1EPONEX 1510 is a diepoxide and commercially available from Hexion Specialty Chemicals.
  	2TOYOBO PMA-KE is an anhydride functional polyolefin and commercially available from Toyobo.

• Charge 1 was added to a 5 L 4-necked flask equipped with a motor driven stainless steel stir blade, a water-cooled condenser, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 40° C. At 40° C., charge 2 was added and held for 15 minutes followed by addition of Charge 3. The reaction mixture was heated to 80° C. and held at 80° C. until beads were dissolved. The reaction mixture was cooled to 60° C. At 60° C., charge 4 was added into reaction mixture and held until it incorporated. Charge 5 was premixed and added into reaction mixture and held until it incorporated. The reaction product was poured out through 5-micron nylon mesh filter bag. The solids content of polyolefin dispersion was 13.5%.
Example E: Preparation of Coumarone Solution
• A Coumarone resin solution was prepared from the following charges:

• 	Ingredients	Parts by weight

  Charge #1

  	Coumarone V-120S1	2018.00
  	AROMATIC 100	1009.00
  	Cyclohexane	1009.00
  	1Coumarone V-120S is commercially available from Nitto Chemical.

• Charge 1 was added to a 12 L 4-necked flask equipped with a motor driven stainless steel stir blade, a water-cooled condenser, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 40° C. and held at 40° C. for 1 hour. Then reaction mixture was heat to 60° C. and held until it incorporated. The reaction product was cooled to 40° C. poured out through 5-micron nylon mesh filter bag. The solids content of polyolefin dispersion was 53.9%.
Example F: Preparation of Polyolefin Solution
• A polyolefin solution was prepared from the following charges:

• 	Ingredients	Parts by weight (g)

  Charge #1

  AROMATIC 100

  2313.70

  Charge #2

  	EPONEX 15101	3.08
  	AROMATIC 100	24.95

  Charge #3

  TOYOBO PMA-LE2

  496.92

  Charge #4

  Cyclohexane

  696.82

  Charge #5

  	Cyclohexane	226.30
  	Isopropanol	84.61
  	1Eponex 1510 is commercially available from Hexion Specialty Chemicals.
  	2Toyobo PMA-LE is an anhydride functional polyolefin and commercially available from Toyobo.

• Charge 1 was added to a 5 L 4-necked flask equipped with a motor driven stainless steel stir blade, a water-cooled condenser, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 40° C. At 40° C., charge 2 was added and held for 15 minutes followed by addition of Charge 3. The reaction mixture was heated to 80° C. and held at 80° C. until beads were dissolved. The reaction mixture was cooled to 60° C. At 60° C., charge 4 was added into reaction mixture and held until it incorporated. Charge 5 was premixed and added into reaction mixture and held until it incorporated. The reaction product was poured out through 5-micron nylon mesh filter bag. The solids content of polyolefin dispersion was 13.2%.
Example G: Preparation of Polyester Modified Polyolefin
• A polyester modified polyolefin solution was prepared from the following charges:

• 	Ingredients	Parts by weight

  Charge #1

  	TOYOBO PMA-LE1	200.00
  	AROMATIC 150	600.00
  	Butyl Acetate	150.00

  Charge #2

  	EPONEX 15102	75.40
  	AROMATIC 150	20.00

  Charge #3

  Butanol

  71.23

  Charge #4

  	ARMEEN DMCD 3	1.83
  	AROMATIC 150	1.49

  Charge #5

  	Cyclohexane	248.60
  	1TOYOBO PMA-LE is an anhydride functional polyolefin and commercially available from Toyobo.
  	2EPONEX 1510 is commercially available from Hexion Specialty Chemicals.
  	3 ARMEEN DMCD (0.5%) is dimethyl cocoamine and commercially available from Akzo Nobel Chemicals.

• Charge 1 was added to a 2 L 4-necked flask equipped with a motor driven stainless steel stir blade, a water-cooled condenser, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 100° C. At 100° C., charge 2 was added and held for 15 minutes. After holding, charge 3 was added and held for 15 minutes. The reaction mixture was stirred at 100° C. until anhydride peaks were gone as measured by IR. Charge 4 was added into reaction mixture and held at 100° C. until acid value is less than 4. The reaction product was cooled to 60° C. by adding charge #5 and poured out through 5-micron nylon mesh filter bag. The solids content of polyolefin resin was 21.18%.
Example H: Preparation of Higher Solid Polyolefin Solution
• A higher solid polyolefin solution was prepared from the following charges:

• 	Ingredients	Parts by weight (g)

  Charge #1

  Butyl acetate

  293.20

  Charge #2

  	EPONEX 15101	1.54
  	Butyl acetate	4.97

  Charge #3

  TOYOBO PMA-LE2

  248.46

  Charge #4

  Cyclohexane

  496.92

  Charge #5

  	Cyclohexane	198.80
  	Isopropanol	42.31
  	1EPONEX 1510 is commercially available from Hexion Specialty Chemicals.
  	2TOYOBO PMA-LE is an anhydride functional polyolefin and commercially available from Toyobo.

• Charge 1 was added to a 2 L 4-necked flask equipped with a motor driven stainless steel stir blade, a water-cooled condenser, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 40° C. At 40° C., charge 2 was added and held for 15 minutes followed by addition of Charge 3. The reaction mixture was heated to 80° C. and held at 80° C. until beads were dissolved. The reaction mixture was cooled to 60° C. At 60° C., charge 4 was added into reaction mixture and held until it incorporated. Charge 5 was premixed and added into reaction mixture and held until it incorporated. The reaction product was poured out through 5-micron nylon mesh filter bag. The solids content of polyolefin dispersion was 19.3%.
Example I: Preparation of an Anhydride and Acrylic Modified Polyolefin Solution
• An anhydride and acrylic modified polyolefin solution was prepared from the following charges:

• 	Ingredients	Parts by weight (g)

  Charge #1

  AROMATIC 100

  462.70

  Charge #2

  	EPONEX 15101	0.62
  	AROMATIC 100	4.99

  Charge #3

  AUROREN S-5297S2

  99.38

  Charge #4

  Cyclohexane

  139.36

  Charge #5

  	Cyclohexane	45.30
  	Isopropanol	16.92
  	1EPONEX 1510 is commercially available from Hexion Specialty Chemicals.
  	2AUROREN S-5297S is an anhydride and acrylic modified polyolefin and commercially available from Nippon Paper Group.

• Charge 1 was added to a 1 L 4-necked flask equipped with a motor driven stainless steel stir blade, a water-cooled condenser, a nitrogen blanket, and a heating mantle with a thermometer connected through a temperature feedback control device. The reaction mixture was heated to 40° C. At 40° C., charge 2 was added and held for 15 minutes followed by addition of Charge 3. The reaction mixture was heated to 80° C. and held at 80° C. until beads were dissolved. The reaction mixture was cooled to 60° C. At 60° C., charge 4 was added into reaction mixture and held until it incorporated. Charge 5 was premixed and added into reaction mixture and held until it incorporated. The reaction product was poured out through 5-micron nylon mesh filter bag. The solids content of polyolefin dispersion was 13.7%.
Example J: Preparation of Acrylic Resin
• An acrylic resin was prepared in a 300 mL continuous stir tank reactor (CSTR) system from the components listed in the table below.

• 	Ingredients	Parts by weight (g)

  Charge #1

  	Hydroxypropyl acrylate1	2320.0
  	Styrene	1160.0
  	Butyl acrylate	1102.0
  	Butyl methacrylate	1073.0
  	Acrylic acid	116.0
  	Methyl methacrylate	29.0
  	Di-t-amyl peroxide1	58.0

  Charge #2

  	Di-t-amyl peroxide	58.0
  	1Hydroxypropyl acrylate is commercially available from BASF.
  	2 Di-t-amyl peroxide is commercially available from Arkema INC.

• The CSTR was charged with 300 mL of Dowanol PM. The charge 1 were weighed and stirred for 15 minutes at an agitation rate sufficient to provide good mixing, then charged to a feed tank while the reactor system was heating up to the reaction temperature (226° C.). Collection of the resulting acrylic resin was begun 15 minutes after the feed was started and continued for 25 minutes. The neat resin was continuously transferred to flash tank where charge 2 was added as a chaser initiator. The flash tank was maintained under pressure at the temperature around 195° C. (not exceed to 200° C.). The resulting material was thinned with a solvent mixture of aromatic 100 and Dowanol PM acetate (weight ratio is 40:60) to a weight percent solid content of 67% (measured for one hour at 110° C.). The final resin was a viscous liquid with a Mw of 8557, a Mn of 2079, and PDI of 4.1.
• The weight average molecular weight was determined by Gel Permeation Chromatography using a Waters 2695 separation module with a Waters 410 differential refractometer (RI detector) and polystyrene standards. Tetrahydrofuran (THF) was used as the eluent at a flow rate of 1 ml min⁻¹, and two PL Gel Mixed C columns were used for separation
Film Forming Compositions: Unpigmented Adhesion Promoters:
• Compositions for Examples 1 and 2 according to the present invention are listed below in Table 1. The amounts listed are the total parts by weight in grams. Each component was mixed sequentially with agitation.

• 	TABLE 1
  	Parts by weight of Component

  Ingredient	Example 1	Example 2

  SOLVESSO 100 1	160.39	160.39
  HARDLEN PMA-KE PO2	238.10	238.10
  Alkyd acrylic resin3	107.46	—
  Coumarone V120S4	—	117.24
  KRATON G1726X Thermoplastic rubber5	22.44	22.44
  Cyclohexane6	160.39	160.39
  CYMEL 11587	14.59	14.59
  Isopropyl alcohol8	20.69	20.69
  DC200 Silicone Solution9	0.04	0.04
  CYCAT 60010	2.06	2.06
  Phenyl acid phosphate11	0.11	0.11
  EFKA PL 5651 NF12	1.08	1.08
  Total	727.34	737.13
  1 Solvent commercially from Exxon Mobil Corporation.
  2Synthesis example D
  3Alkvd acrylic resin: Synthesis example C
  4Synthesis example E
  5Resin solution containing 25% KRATON G1726X, commercially available from Kraton Polymers, AND 75% SOLVESSO 100, available from Exxon Mobil Corporation.
  6Solvent commercially available from Brenntag.
  7High-imino melamine commercially available from Allnex.
  8Solvent commercially available from Dow Chemical.
  9Additive solution containing ANDISIL SF100 commercially available from AB Specialty Silicones LLC.
  10Catalyst commercially available from Allnex.
  11Catalyst commercially available from Islechem LLC.
  12Additive commercially available from BASF.

Pigmented Adhesion Promoters:
• Compositions for Pigment Pastes 1-4 are listed below in Table 2. The amounts listed are the total parts by weight in grams. Ingredients of the grind except the methyl n-amyl ketone are added sequentially together and mixed with a Cowles blade before entering the mill. A mill is used to grind the mixture to a Hegman of 7.25. The methyl n-amyl ketone is added at the end as a mill wash.

• 	TABLE 2
  	Parts by weight of Component

  	Pigment	Pigment	Pigment	Pigment
  Ingredient	Paste 1	Paste 2	Paste 3	Paste 4

  SOLVESSO 100 1	46.42	46.42	27.66	26.48
  SOLVESSO 150 1	8.77	8.77	5.23	8.77
  Alkyd acrylic resin 3	58.17	58.17	—	58.17
  Coumarone V120S4	—	—	60.55	—
  KRATON G1726X Thermoplastic	22.44	22.44	22.44	22.44
  rubber5
  PRINTEX XE 2-B13	7.67	7.67	7.67	7.67
  VM&P Naptha14	34.98	34.98	20.85	34.98
  White tint15	126.78	25.78	25.78	126.78
  Methyl N-amyl ketone16	36.04	36.04	—	36.04
  Total	341.27	240.25	170.17	321.34
  1 Solvent commercially from Exxon Mobil Corporation.
  3 Alkyd acrylic resin: Synthesis example C
  4Synthesis example E
  5Resin solution containing 25% KRATON G1726X, commercially available from Kraton Polymers, AND 75% SOLVESSO 100, available from Exxon Mobil Corporation.
  13Carbon black available from Orion Engineered Carbons.
  14Solvent available from Ashland Inc.
  15Titanium dioxide pigment paste dispersion of 64.25% titanium dioxide pigment available from The Chemours Company LLC, 11.24% alkyd (Synthesis example B), 23.53% SOLVESSO 100 (available from Exxon Mobil Corporation) and 0.98% xylene.
  16Solvent available from Dow Chemical Co.

• The Pigment Pastes 1-4 were used in Examples 3-11. Compositions for Examples 3-11 are listed below in Tables 3-4. (Note that Example 8 is comparative; the composition does not contain an aminoplast.) The amounts listed are the total parts by weight in grams. Each component was mixed sequentially with agitation.

• 	TABLE 3
  	Parts by weight of Component

  Ingredient	Example 3	Example 4	Example 5	Example 6

  Pigment Paste 1	341.27	—	—	—
  Pigment Paste 2	—	240.25	—	—
  Pigment Paste 3	—	—	170.17	—
  Pigment Paste 4	—	—	—	321.34
  TOYO-TAC PMA-KE	238.10	—	—	—
  PO2
  TOYO-TAC PMA-LE	—	151.17	151.17	—
  PO17
  Modified PMA-LE PO18	—	—	—	97.23
  White tint15	—	101.01	101.01	—
  SOLVESSO 100 1	87.68	87.68	87.68	107.62
  Cyclohexane6	87.68	87.68	87.68	87.68
  Coumarone V120S4	25.28	45.28	45.28	42
  CYMEL 11587	14.59	14.59	14.59	14.59
  Isopropyl alcohol8	20.69	20.69	20.69	20.69
  DC200 Silicone	0.04	0.04	0.04	0.04
  Solution9
  CYCAT 60010	2.06	2.06	2.06	2.06
  Phenyl acid	0.11	0.11	0.11	0.11
  phosphate11
  EFKA PL 5651 NF12	1.08	1.08	1.08	1.08
  Total	700.72	751.64	681.56	694.43

• 	TABLE 4
  	Parts by weight of Component

  		Example 8
  Ingredient	Example 7	(Comparative)	Example 9	Example 10	Example 11

  Pigment Paste 4	321.34	321.34	321.34	321.34	321.34
  TOYO-TAC PMA-LE	103.52	103.52	103.52	—	—
  PO19
  AUROREN S-5297S20	—	—	—	145.56	145.56
  SOLVESSO 100 1	107.62	107.62	107.62	107.62	107.62
  Cyclohexane6	87.68	87.68	87.68	87.68	87.68
  Coumarone V120S4	42	63.12	38.29	42	—
  Acrylic resin21	—	—	12.45	—	—
  Alkyd acrylic 3	—	—	—	—	41.5
  CYMEL 11587	14.59	—	6.41	14.59	14.59
  Isopropyl alcohol8	20.69	20.69	20.69	20.69	20.69
  DC200 Silicone	0.04	0.04	0.04	0.04	0.04
  Solution9
  CYCAT 60010	2.06	2.06	2.06	2.06	2.06
  Phenyl acid	0.11	0.11	0.11	0.11	0.11
  phosphate11
  EFKA PL 5651 NF12	1.08	1.08	1.08	1.08	1.08
  Total	700.72	707.25	701.29	742.76	742.26
  1 Solvent commercially from Exxon Mobil Corporation.
  2 Synthesis example D
  3 Synthesis example C
  4Synthesis example E
  6Solvent commercially available from Brenntag.
  7Melamine commercially available from Allnex.
  8Solvent commercially available from Dow Chemical.
  9Additive solution containing ANDISIL SF100 commercially available from AB Specialty Silicones LLC.
  10Catalyst commercially available from Allnex.
  11Catalyst commercially available from Islechem LLC.
  12Additive commercially available from BASF.
  15 Titanium dioxide pigment paste dispersion of 64.25% titanium dioxide pigment available from The Chemours Company LLC, 11.24% alkyd (Synthesis example B), 23.53% SOLVESSO 100 (available from Exxon Mobil Corporation) and 0.98% xylene.
  17 Synthesis example F
  18 Synthesis example G
  19Synthesis example H
  20Synthesis example I
  21Synthesis example J

• Coatings were applied to Lyondell Basell Hifax TRC779X (4″×12″×0.118″) thermoplastic olefin (TPO) panels, available from Standard Plaque Inc.
• For Examples 1-5, LBC408YB, an orange metallic solventborne basecoat and TKU2000CS 2K isocyanate clearcoat, both available from PPG, were applied over the adhesion promoters. Adhesion promoter, basecoat and clearcoat were applied wet-on-wet-on-wet via hand spray application targeting dry film thicknesses of 5-10, 16-20 and 38-46 microns respectively. All flashes between coating layers and before the cure oven were untimed at ambient conditions. The system was baked for 35 minutes at 180° F. (82° C.) in a horizontal position.
• For Examples 6-11, LBC8555B, a black pigmented solventborne basecoat and TKU2000CS 2K isocyanate clearcoat, both available from PPG, were applied over the adhesion promoters. Adhesion promoter, basecoat and clearcoat were applied wet-on-wet-on-wet via automated spray applied targeting dry film thicknesses of 5-10, 16-20 and 38-46 microns respectively. Adhesion promoter was applied in one coat with a 4-minute ambient flash before basecoat application. The basecoat was applied in two coats with 60-second ambient flash between coats and a 4-minute ambient flash before clearcoat. Clearcoat was sprayed in 2 coats with a 60-second ambient flash between coats and a 7-minute ambient flash before entering the cure oven. The system was baked for 35 minutes at 180° F. (82° C.) in a vertical position. A coating system without adhesion promoter was sprayed as a negative control.
• Coated panels were allowed to rest under ambient conditions for at least 3 days before testing. Panels were tested for resistance to delamination in a fuel soak test. Results follow in Table 5.

• 	TABLE 5
  	Adhesion Promoter	Fuel Resistance22 (minutes)

  	Example 1	32
  	Example 2	29
  	Example 3	60
  	Example 4	60
  	Example 5	32
  	Example 6	60
  	Example 7	60
  	Example 8	7
  	Example 9	60
  	Example 10	60
  	Example 11	60
  	None	2
  	22Coated panels were cut into three 1″ × 4″ pieces for each coating system to be tested for fuel resistance. Cut edges were covered using Nichiban LP-24 tape available from Alliance Rubber Co. An “X” was cut into the coating layers on one end of each panel and that end was submersed in a synthetic fuel blend (formulation in Table 6). Panels were timed from the time they were submerged in the fuel until the time the coating started to lift from the “X.” The time at which the coating lifted from the substrate was recorded as the time to fail. The times to fail for the three panels for each coating system were averaged, rounded to the nearest whole value and listed as Fuel Resistance;, higher times indicate better fuel resistance. Test specifications for a “pass” rating require at least 15 minutes in the fuel soak before lifting of the coating from the substrate is observed.

• TABLE 6
  Synthetic Fuel formulation

  		Parts by weight of
  	Ingredient	Component

  	2,2,4-trimethylpentane23	25.35
  	Toluene24	42.25
  	di-isobutylene23	12.68
  	Ethanol SDA-3A 200	4.22
  	PROOF25
  	Methanol24	15.00
  	Deionized water	0.50
  	Total	100.00
  	23Solvent commercially available from Fisher Scientific.
  	24Solvent commercially available from Ashland Inc.
  	25Solvent commercially available from Brenntag.

• Whereas particular embodiments of this invention have been described above for purposes of illustration, it will be evident to those skilled in the art that numerous variations of the details of the present invention may be made without departing from the scope of the invention as defined in the appended claims.

Claims (23)

Therefore, we claim:

1. A solventborne film-forming composition comprising:

a) a non-chlorinated, linear polyolefin polymer prepared from a reaction mixture comprising 0.5 to 5 percent by weight maleic anhydride based on the total weight of monomers in the reaction mixture;

b) an aminoplast: and

c) a polymer component comprising:

i) an addition polymer prepared from a reaction mixture comprising coumarone; and/or

ii) an alkyd resin.

2. The composition of claim 1 wherein the linear polyolefin polymer a) is dispersed in an organic medium with a polyepoxide and a monohydric alcohol.

3. The composition of claim 2 wherein the monohydric alcohol comprises n-propanol, isopropanol, n-butanol, and/or isobutanol.

4. The composition of claim 1 wherein the linear polyolefin polymer a) is further reacted with a polyepoxide and a monohydric alcohol.

5. The composition of claim 4 wherein the monohydric alcohol comprises n-propanol, isopropanol, n-butanol, and/or isobutanol.

6. The composition of claim 1 wherein the reaction mixture used to prepare the linear polyolefin polymer a) further comprises an ethylenically unsaturated monomer comprising at least one (meth)acrylic monomer.

7. The composition of claim 1 wherein the aminoplast is at least partially alkylated and wherein 10 to 35 percent of functional groups on the aminoplast comprise imino groups.

8. The composition of claim 1 wherein the polymer component c) comprises an addition polymer prepared from a reaction mixture comprising coumarone, indene, and styrene.

9. The composition of claim 1 wherein the polymer component c) comprises i) an addition polymer prepared from a reaction mixture comprising coumarone, indene, and styrene; and ii) an alkyd resin.

10. The composition of claim 1, further comprising a colorant.

11. The composition of claim 1, further comprising a hydroxyl functional (meth)acrylic polymer and/or a hydroxyl functional polyester polymer.

12. A method of improving fuel resistance of a coated article, comprising:

(1) applying a first film-forming composition to at least a portion of a substrate to form a coated substrate, wherein the first film-forming composition is solventborne and comprises:

a) a non-chlorinated, linear polyolefin polymer prepared from a reaction mixture comprising 0.5 to 5 percent by weight maleic anhydride based on the total weight of monomers in the reaction mixture;

b) an aminoplast: and

c) a polymer component comprising:

i) an addition polymer prepared from a reaction mixture comprising coumarone; and/or

ii) an alkyd resin;

(2) applying a second, curable film-forming composition to at least a portion of the coated substrate formed in step (1) to form a multi-layer coated substrate; and

(3) heating the multi-layer coated substrate formed in step (2) to a temperature and for a time sufficient to cure the second, curable film-forming composition; wherein the substrate comprises an elastomeric, plastic, or composite material.

13. The method of claim 12 wherein the linear polyolefin polymer a) is dispersed in an organic medium with a polyepoxide and a monohydric alcohol.

14. The method of claim 13 wherein the monohydric alcohol comprises n-propanol, isopropanol, n-butanol, and/or isobutanol.

15. The method of claim 12 wherein the linear polyolefin polymer a) is further reacted with a polyepoxide and a monohydric alcohol.

16. The method of claim 15 wherein the monohydric alcohol comprises n-propanol, isopropanol, n-butanol, and/or isobutanol.

17. The method of claim 12 wherein the reaction mixture used to prepare the linear polyolefin polymer a) further comprises an ethylenically unsaturated monomer comprising at least one (meth)acrylic monomer.

18. The method of claim 12 wherein the aminoplast is at least partially alkylated and wherein 10 to 35 percent of functional groups on the aminoplast comprise imino groups.

19. The method of claim 12 wherein the polymer component c) comprises an addition polymer prepared from a reaction mixture comprising coumarone, indene, and styrene.

20. The method of claim 12 wherein the polymer component c) comprises i) an addition polymer prepared from a reaction mixture comprising coumarone, indene, and styrene; and ii) an alkyd resin.

21. The method of claim 12, wherein the first film-forming composition further comprises a colorant.

22. The method of claim 12, wherein the first film-forming composition further comprises a hydroxyl functional (meth)acrylic polymer and/or a hydroxyl functional polyester polymer.

23. The method of claim 12 wherein the multi-layer coated substrate is heated to a temperature up to 135° C. in step (3).