EP0274466A1 - Schutzüberzüge auf basis von melamin für thermoplastische substrate - Google Patents

Schutzüberzüge auf basis von melamin für thermoplastische substrate

Info

Publication number
EP0274466A1
EP0274466A1 EP86904600A EP86904600A EP0274466A1 EP 0274466 A1 EP0274466 A1 EP 0274466A1 EP 86904600 A EP86904600 A EP 86904600A EP 86904600 A EP86904600 A EP 86904600A EP 0274466 A1 EP0274466 A1 EP 0274466A1
Authority
EP
European Patent Office
Prior art keywords
diacids
diols
composite
carbon atoms
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP86904600A
Other languages
English (en)
French (fr)
Inventor
Clayton Byerley Quinn
Richard Robert Mcclish
James Eugene Moore
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
General Electric Co
Original Assignee
General Electric Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Publication of EP0274466A1 publication Critical patent/EP0274466A1/de
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/0427—Coating with only one layer of a composition containing a polymer binder
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/043—Improving the adhesiveness of the coatings per se, e.g. forming primers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04—Coating
    • C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2461/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers

Definitions

  • thermoplastic articles protected by thermoformable a ⁇ tinoplast based mar- and solvent- resistant coatings More particularly, this invention relates to thermoformable protective coatings applied to thermoplastic substrates containing an aminoplast derived component, a polyester polyol, and, optionally, other ingredients.
  • plastics have become commercially vital materials used in a wide range of applications. Particularly, plastics may be applied as transparent articles, as translucent articles, or to opaque surfaces to provide texture, shine, and durability. Generally, these 1 applications require a high degree of abrasion resistance in addition to other required properties, for example, impact strength, tensile strength, or elongation.
  • the coatings technology may be used to join a substrate possessing high impact resistance, tensile strength, non-opacity, and elongation resistance, such as for example, a polycarbonate substrate, with an outer surface coating possessing high abrasion resistance, and low susceptibility to attack by solvents such as for example, an etherified aminoplast derived coating to produce a single article possessing the structural strength of the polycarbonates and the resistance to -2- surface attack of the etherified aminoplast derivatives.
  • Coatings suitable for use on plastic substrates must also possess other secondary properties which render them useable.
  • a coating applied for abrasion resistance must also be compatible with the substrate, have good adhesion to the substrate and preferably, be weather resistant, thermoformable, and solvent resistant. It is often in secondary properties that a particular coating may be judged unsuitable for use in any particular application. Therefore, it is in the secondary properties that much effort for improvement is directed.
  • U.S. Pat. No. 4,197,392 assigned to the same assignee as the present invention, discloses a UV resistant transparent coating for plastic materials containing a mela ine, a polyol, and a benzophenone. This coating has both weather" resistance and thermoformability, however a greater degree of these two properties is desirable.
  • Copending patent application U.S Serial No. 641,914 filed August 17, 1984 discloses aminoplast derived protective coatings for thermoplastic substrates. These coatings contain specific polycaprolactone polyester polyols as a critical polyester polyol component.
  • an object of the present invention to provide protective coating compositions which may be applied to plastic substrates, particularly polycarbonate substrates to impart abrasion resistance and solvent resistance with improved adhesion.
  • the diacids comprise at least 50% by number aliphatic diacids in which the carboxylic acid groups are separated by at least two intervening carbon atoms
  • the diols comprise at least 50% by number aliphatic diols in which carbon atoms containing hydroxyl groups are separated by at least three intervening carbon atoms
  • the polyol content results in an average hydroxyl functionality which is from about 2 to about 3
  • the hydroxyl number is from about 50 to about 175.
  • the coating may further comprise: -4-
  • ultraviolet light stabilizers or absorbers (e) ultraviolet light stabilizers or absorbers, and, (f) other additives or reactants.
  • the substrate is a polycarbonate substrate.
  • thermoplastic resinous substrates which may be used include acetal homopolymers; acetal copolymers produced by polymerization of trioxane and ethylene oxide; epoxy resins; polycarbonates; pol (ester-carbonate) ; polyetherimides; phenylene oxide based resins such as polyphenylene oxide and blends of polyphenylene oxide and styrene resins; polyaryl ethers; polyesters; polyethylene ⁇ ; polyphenylene sulfides; polypropylene; polysulfones; ethylene polymers such as ethyl vinyl acetates; and blends thereof with necessary compatibilizers.
  • the substrate is preferably a thermoplastic resinous polycarbonate, particularly an aromatic polycarbonate.
  • thermoplastic resinous polycarbonate particularly an aromatic polycarbonate.
  • These are homopolymers and copolymers and mixtures thereof that are prepared by reacting a dihydric phenol with a carbonate precursor.
  • Suitable dihydric phenols of the bisphenol type are available and disclosed in U.S. Pat. Nos. 2,999,835, 3,028,365 and 3,334,154 which are incorporated herein by reference.
  • the a inoplasts for use herein are amine-aldehyde reaction products, i.e., aldehyde condensation products of amine compounds.
  • the aldehyde employed is formaldehyde, although the products can be made from other aldehydes, such as acetaldehyde, crotonaldehyde, acrolein, benzaldehyde, furfural and others.
  • Suitable amines for use herein are for example, those of melamine, urea, triazines, diazines, triazoles, guanidines, guanamines, and alkyl and aryl -5- substituted derivatives of such compounds including alkyl and aryl substituted melamine provided at least two amino groups are present.
  • inoplasts contain ethylol or similar alkylol groups, the structure of the alkylol group depending upon the particular aldehyde employed. At least a portion, i.e., all or part, of these alkylol groups should be etherified by reaction with an alcohol.
  • Any monohydric alcohol can be employed for this purpose, including aliphatic alcohols such as methanol, ethanol, propanol, butanol, and other alkanols, usually having up to about 6 carbon atoms; aromatic alcohols; such as benzyl alcohol cyclic alcohols such as cyclohexanol; monoethers of glycols such as the Cello-Solves and Carbitols; and halogen-substituted or other substituted alcohols such as 3-chloropropanol.
  • aliphatic alcohols such as methanol, ethanol, propanol, butanol, and other alkanols, usually having up to about 6 carbon atoms
  • aromatic alcohols such as benzyl alcohol cyclic alcohols such as cyclohexanol
  • monoethers of glycols such as the Cello-Solves and Carbitols
  • halogen-substituted or other substituted alcohols such as 3-chloropropano
  • the preferred aminoplast derived component of the coating composition of this invention is an amine-aldehyde-alcohol of the general formula:
  • R" 1 is independently selected from H, -CH.OH, and -CH,0(CH.,) H, wherein e is an integer from 1 to 6, i and is selected from H, -OH, -CH 3 and -N(R I , ') 2 .
  • R 1V is -NfR*" ⁇ and all R' * ' are an alkoxymethyl, particularly, methoxymethyl.
  • aminoplast derived component is produced in a manner well known in the art using acidic or basic catalyst and varying conditions of time and temperature in accordance with conventional practice.
  • the aldehyde is often employed as a solution in water or alcohol and the condensation, etherification, and polymerization reactions may be carried out either sequentially or simultaneously.
  • CYMEL 301 hexamethoxymethylmelamine is commercially available from American Cyanamid Company. This aminoplast derivative is a clear liquid with a specific gravity of 1.2, refractive index of 1.515-1.520, a free formaldehyde percent maximum of 0.30, a low free ethylol content, an equivalent weight of 130-190, and a vapor pressure, 180 ⁇ C f mm of 0.02-0.03.
  • polyester polyols suitable for use herein are principally the reaction products of diacids and diols wherein the diacids comprise at least 50% by number aliphatic diacids in which the carboxylic acid groups are separated by at least two, preferrably four, intervening carbon atoms, ana the diols comprise at least 50% by number aliphatic diols in which carbon atoms containing hydroxyl groups are separated by at least two, preferrably four, intervening carbon atoms.
  • Suitable diacids for the at least 50% portion aliphatic diacids include succinic acid, glutaric acid, adipic acid, suberic acid, sebacic acid, azelaic acid, 1,12-dodecanedioic acid, 2,2,4- and
  • the at least 50% portion aliphatic diacid is adipic acid.
  • Suitable for use as the remaining diacids are unsaturated dicarboxylic acids, i.e., maleic acid, fumaric acid, itaconic acid,, citraconic acid, etc.; cycloaliphatic diacids, i.e., 1,2-cyclohexanedicarboxylic anhydride, tetrahydrophthalic anhydride, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxvlic acid, etc.; and aromatic diacids, i.e., phthalic acid, isophthalic acid. -7- terephthalic acid, etc.
  • the at least 50% portion aliphatic diacids are 100% of the diacids.
  • Suitable diols for the at least 50% portion aliphatic diols include glycols of the formula HO(CH 2 ) OH wherein n equals 4-12 and methyl, ethyl, phenyl, etc., substituted derivatives thereof.
  • Specific aliphatic diols include 1,6-hexanediol, 3-methyl-l,5-pentanediol, 2,2,4-trimethyl-l,5-pen- tanediol, etc. Preferred for use is 1,6-hexanediol.
  • Suitable for use as the remaining diol are short chain aliphatic diols, i.e., 1,3-butanediol, 1,3-propylene glycol, 2,2-diethyl-l,3-propanediol, ethylene glycol, neopentyl glycol, etc.; aromatic diols, i.e., , f -methylenebis (cyclohexanol) , 4,4'-isopropylidene- bis (cyclohexanol) , phenylenedipropanols, etc.; and cycloaliphatic diols, i.e., 1,4-cyclohexanedimethanol, etc.
  • the diols in which carbon atoms con ⁇ taining hydroxyl groups sepa ated by at least two, preferrably four, intervening carbon atoms are 100% of the diols.
  • polyester polyols may be adjusted by the addition of various polyol monomers having hydroxy functionalities of three or greater, in amounts effective to produce an average functionality of from about 2 to about 3.
  • a single triol may be used in combination with various diacids and diols to produce a trifunctional hydroxy terminated polyester polyol.
  • Suitable triols include trimethylol propane, trimethylolethane, 1,2,3-propane- triol, 1,2,4-butanetriol, 1,2,6-hexanetriol, etc.
  • quadrifunctional polyols such as pentaerythritol may be used to achieve the same average functionality.
  • the average hy ⁇ droxy functionality of the polyester polyol may be varied between about 2 and about 3, preferably, it is about 2. -8-
  • Preparation of the polyester polyol is accomplished by using known processes employed in preparing polyesters.
  • the components of the polyester polyol can be reacted together in a single stage, i.e., all of the reactants are added to the reactor at the same time, or in several stages wherein the polyol and a portion of the acid are first reacted to form a partial ester, following which the remainder of the acid is reacted with the partial ester to form the finished ester.
  • the equivalent ratio of total acid content to total alcohol content ranges from about 1:1.25 to about 1:1.1.
  • the degree of polymerization during the reaction is controlled such that the hydroxyl number of the finished ester ranges, on average, from about 50 to about 175; and preferably, from about 100 to about 150.
  • the solvent used in the preparation of the coating composition includes alcohols, ketones, esters, ethers, alkoxy alkanols, halogenated compounds, carboxylic acids, aromatic compounds, or the like, which may be used alone or in a combination of two or more thereof.
  • Particularly suitable examples of the solvent are lower alcohols (e.g. methanol, ethanol, propanol or butanol) and alkoxy alkanols (e.g. methyl cellosolve, ethyl cellosolve or butyl cellosolve) .
  • the solvent employed must not injure the substrate to which the coating composition is applied, that is, it must be nonagressive yet it must be capable of dissolving the aminoplast derivative and in particular the polyester polyol.
  • the solvent should be of such a volatility that it can be easily evaporated and removed from the coating composition at temperatures below cure temperature.
  • a suitable, nonagressive solvent for a given substrate -9- and a given polyester polyol may be. readily determined by one skilled in the art.
  • the preferred solvent is butyl cellosolve.
  • Suitable catalysts are alkyl acid phosphates, such as onomethyl acid phosphate, onoethyl acid phosphate, onopropyl acid phosphate and monobutyl acid phosphate, as well as the corresponding dialkyl compounds, such as dibutyl acid phosphate.
  • alkyl acid phosphates such as onomethyl acid phosphate, onoethyl acid phosphate, onopropyl acid phosphate and monobutyl acid phosphate, as well as the corresponding dialkyl compounds, such as dibutyl acid phosphate.
  • a mixture of mono- and dialkyl phosphates is often utilized.
  • alkyl acid phosphates examples include phosphoric acid, maleic acid and anhydride, fumaric acid, chloro aleic acid and anhydride, alkyl acid phthalates such as methyl, ethyl, propyl and butyl acid phthalates, monoalkyl succinates and maleate ⁇ such as methyl, ethyl, propyl and butyl succinates and maleates and others having sufficient solubility to permit them to be dissolved in the coating composition at the desired proportion.
  • Catalysts which have been found to be particularly suitable are compounds such as the sulfonic acids and derivatives thereof including, for example, p-toluene sulfonic acid, methyl-p-sulfonic acid and the like.
  • Protective coating compositions which are to be prepared in advance of or stored prior to application and cure require reaction stabilizers or stabilizers to deactivate the catalyst until cure. It is within the skill of the art to determine a suitable stabilizer for use with a given catalyst.
  • the preferred catalyst of the instant invention p-toluene sulfonic acid as well as others may be stabilized with equimolar amounts of a suitable amine stabilizer, for example, methylaminoethanol, triethylamine, 2-amino - 2-methyl-l-propanol but preferably the stabilizer is triethylamine.
  • Any suitable ultraviolet stabilizer may be used in the present invention at any concentration effective to protect the thermoplastic substrate from the degradative effects of light. Suitable ultraviolet absorbers are for example benzophenone derivatives, including: 2,2'4,4'-tetrahydroxybenzophenone;
  • Suitable benzotriazole derivatives may also be employed including 2-(2'-hydroxy-5'-methylphenyl) -benzotriazole, 2-(2'-hydroxy-3*-methyl-5'-tert- butylphenyl)-benzotriazole, 2-(2 • -hydroxy-3'-di-tert -butylphenyl)-benzotriazole and derivatives of crotonic acid such as a-cyano-b methyl-b-(p-methoxyphenyl)-crotonic acid methyl ester, a-cyano-b-N-(2-methyl-indolinyl)crotonic acid methyl ester, substituted acrylates such as 2 ethyl-hexyl-2-cyano-3,3-diphenyl acrylate as well as malonic acid esters such as, for example, the dimethyl, diethyl, dipropyl and the like esters of malonic acid and the like and mixtures thereof.
  • crotonic acid such as
  • dihydroxybenzophenones such as: 2,4-dihydroxybenzophenone,2,2*-dihydroxybenzophenone, 2-hydroxy-5-aminobenzophenone , 2,2' ,4,4'-tetrahydroxybenzophenone, 2,2* ,5,5'-tetrahydroxybenzophenone, dihydroxyanthrophenones, dihydroxyanthrones, etc.
  • Other hydroxy functional reactants and additives may be added to the coating composition of the present -1 1- invention, in addition to the polyester polyol. Hydroxy alkyl esters of addition polymerized unsaturated carboxylic acids, i.e., hydroxy functional polyacrylates or poly ethacrylates may be useful to increase certain properties of the cured coating.
  • aliphatic diols i.e., the alkylene diols.
  • the protective coating composition may be blended by mixing the aminoplast derived component, the polyester polyol, an appropriate, nonagressive solvent, a catalyst, and optionally, a reaction stabilizer, UV stabilizer, and other additive or reactant.
  • a reaction stabilizer Preferably for each weight part polyester polyol there should be present from about 0.5 to about 3 and most preferably, from about 2/3 to about 7/3 parts by weight aminoplast derived component.
  • the solvent should be added in sufficient amount to produce from about 15% to about 75% solids.
  • the amount of catalyst, reaction stabilizer, and UV stabilizer which should be added is well within the determination of one skilled in the art. Of course, where other hydroxy functional reactants are present, the amount of aminoplast derivative necessary may be greater.
  • the protective coating composition may be applied to the thermoplastic substrate by any of the well known means. Spraying, dipping, roll coating, and the like are appropriate coating techniques. The parameters of the coating technique chosen should be adjusted so as to produce a cured protective coating having a thickness of from about 0.05 to about 1 mil. Preferably the thickness should be about 0.2 mils.
  • the preferred method of curing the applied coating composition is by heat curing.
  • the coated -12- substrate may be heated in ovens by infrared radiation, by microwave, etc.
  • the solvent used in the coating composition should be substantially evaporated before the reaction or cure temperature of the coating is reached.
  • the sample is tested in accordance with the procedure of ASTM D-3359 Method B. Samples which attain a rating of 5B in the ASTM standard are given a "Pass”. Samples which show any flaking or detachment of the squares in the lattice are given a "Fail”. Taber Abrasion Test (Abrasion Test) The sample is tested in accordance with the procedure of ASTM D-1044-78 using a CS-10F wheel, 500g load, and 100 cycles. The reported figure is the percentage of transmitted light that is scattered by the abraded specimens.
  • the sample is heated to forming temperature and formed around a 1"radius mandrel.
  • the sample is rated "Fail” if upon visual inspection any cracking, flaking, or detachment of the coating is observed.
  • the sample is tested in accordance with the above Cross Hatch Adhesion Test and immersed in a 65°C water bath.
  • the reported figure is the number of days which the sample is -13- soaked before any flaking or detachment of the squares in the lattice is observed in subsequent adhesion tests.
  • Examples 1-4 The following polyols were combined with CYMEL 301, butyl cellosolve, and a catalyst mixture having 20% by weight p-toluenesulfonic acid and 80% by weight 2-propanol in the gram weight proportions shown below.
  • the resulting coating composition was dip coated onto a 1/8" BPA polycarbonate panel and cured to a noncritical thickness of less than 1 mil at a temperature of 130°C for 2 hours.
  • Thermoform Test atersoak Test 1-3
  • the resulting coating composition was dip coated onto a 1/8" BPA-polycarbonate panel and cured to a noncritical thickness of less than 1 mil at a temperature of 130 ⁇ C for 2 hours.
  • Adhesion Test Pass Pass Fail Fail Pass Abrastion Test 8.8 10.4 34.6 7.4 8.2 Thermoform Test atersoak Test 1-3 1-3
  • the resulting coating composition was dip coated onto a 1/8" BPA-polycarbonate panel and cured to a noncritical thickness of less than 1 mil at a temperature of 130°C for 2 hours.
  • the resulting coating composition was dip coated onto a 1/8" BPA-polycarbonate panel and cured to a noncritical thickness of less than 1 mil at a temperature of 130°C for 2 hours.
  • the resulting coating composition was dip coated onto a 1/8" BPA-polycarbonate panel and cured to a noncritical thickness of less than 1 mil at a temperature of 130°C for 2 hours.
  • Table 7 Table 7
  • UV Stabilizer 1 11.9 Reaction Stabilizer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Paints Or Removers (AREA)
EP86904600A 1986-07-02 1986-07-02 Schutzüberzüge auf basis von melamin für thermoplastische substrate Withdrawn EP0274466A1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1986/001389 WO1988000218A1 (en) 1986-07-02 1986-07-02 Melamine based protective coatings for thermoplastic substrates

Publications (1)

Publication Number Publication Date
EP0274466A1 true EP0274466A1 (de) 1988-07-20

Family

ID=22195560

Family Applications (1)

Application Number Title Priority Date Filing Date
EP86904600A Withdrawn EP0274466A1 (de) 1986-07-02 1986-07-02 Schutzüberzüge auf basis von melamin für thermoplastische substrate

Country Status (3)

Country Link
EP (1) EP0274466A1 (de)
JP (1) JPH01500038A (de)
WO (1) WO1988000218A1 (de)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7972656B2 (en) 2006-03-31 2011-07-05 Sdc Technologies, Inc. Coating compositions, articles, and methods of coating articles
US8153197B2 (en) 2004-10-12 2012-04-10 Sdc Technologies, Inc. Coating compositions, articles, and methods of coating articles

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7960031B2 (en) 2004-06-30 2011-06-14 Sabic Innovative Plastics Ip B.V. Coated sheet, method of formation thereof, and articles derived therefrom

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Publication number Priority date Publication date Assignee Title
US3804920A (en) * 1972-03-29 1974-04-16 Sherwin Williams Co Resin compositions
JPS51126264A (en) * 1975-04-25 1976-11-04 Mitsubishi Chem Ind Agent for treating surface of synthetic resin product
CA1091106A (en) * 1976-03-22 1980-12-09 Joseph M. Rich Coated polycarbonates
US4201832A (en) * 1978-06-23 1980-05-06 General Electric Company Non melt-drip flame retardant polycarbonate composition
EP0034919B1 (de) * 1980-02-20 1986-01-02 Whittaker Corporation Verzweigte Polyester für Klebstoff- und Überzugszusammensetzungen
GB2125421B (en) * 1982-08-17 1986-07-23 Nippon Paint Co Ltd Coating composition and coated article
US4552936A (en) * 1984-08-17 1985-11-12 General Electric Company Weatherable abrasion resistant etherified aminoplast derived coating for plastic substrates

Non-Patent Citations (1)

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Title
See references of WO8800218A1 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8153197B2 (en) 2004-10-12 2012-04-10 Sdc Technologies, Inc. Coating compositions, articles, and methods of coating articles
US8153196B2 (en) 2004-10-12 2012-04-10 Sdc Technologies, Inc. Coating compositions, articles, and methods of coating articles
US8158191B2 (en) 2004-10-12 2012-04-17 Sdc Coatings, Inc. Coating compositions, articles, and methods of coating articles
US7972656B2 (en) 2006-03-31 2011-07-05 Sdc Technologies, Inc. Coating compositions, articles, and methods of coating articles

Also Published As

Publication number Publication date
JPH01500038A (ja) 1989-01-12
WO1988000218A1 (en) 1988-01-14

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