Sulfonimide catalysts polyfunctional material combination

Description

FIELD OF THE INVENTION
This invention relates to the use of sulfonimide cure catalysts in combination with aminoplast crosslinkers and their use in curable compositions.
BACKGROUND OF THE INVENTION
Alkyl and aryl sulfonic acids have found utility in industry as "strong acid" catalysts capable of activating acid-sensitive curable compositions to produce cured coatings, moulded articles or adhesives.
U.S. Pat. No. 3,927,141 and U.S. Pat. No. 4,118,437 disclose powder coating compositions containing alkoxyalkyl groups carrying aminoplasts which are cured with an acid catalyst including sulfonic acids, and U.S. Pat. No. 4,064,191 discloses organic solvent-based compositions thereof.
It is well known in the art that strong acids such as sulfonic generally favor rapid cure. However, it is suggested in U.S. Pat. No. 4,031,036, that acid strength alone does not always determine effectiveness of a catalyst in complex reactions. In many cases, strong acids produce less than "smooth" surfaces having a "sandpaper-like" appearance. Furthermore, because of the extreme reactivity of sulfonic acid catalysts, curable powders containing them have been unsatisfactory because of poor package stability. The poor package stability is associated with room temperature crosslinking of the curable powders catalyzed by the excessively strong sulfonic acid catalysts. As a result, the low temperature reaction often causes clumping and sintering or fusing of the powdered resin. These are undesirable because they impair fluidization of the powder during application contributing to the production of non-uniform coatings with diminished gloss.
As a partial solution for low temperature crosslinking, U.S. Pat. No. 4,510,290 and U.S. Pat. No. 4,281,075 disclose the use of latent-reactive sulfonic acid catalysts such as benzoin tosylates and beta-hydroxy tosylates, respectively. The chemistry of the beta-hydroxy tosylate latent acid catalysts is described in Ind. Eng. Chem. Prod. Res. Dev., 22, 440 (1983). Even though latent catalyst approach improves the shelf-life of the cure catalyst-containing powder coating compositions, the overall film properties and appearance of the cured films have been no better than non-latent sulfonic acid catalyzed systems because the active catalyst in both systems is the same: a sulfonic acid.
Powder coating technology is dominated by isocyanate crosslinked and epoxide crosslinked reaction systems which are of relatively high cost. Improved crosslinking systems based on aminoplast resins when used in combination with solid components offer cost attractive alternative powder coating formulations.
This invention provides sulfonimides as improved catalysts useful in the curing of aminoplast crosslinkable resin compositions with particular utility in powder coatings/formulations.
SUMMARY OF THE INVENTION
This invention is a curable composition comprising:
(i) a sulfonimide cure catalyst,
(ii) an aminoplast crosslinking agent containing at least 2 crosslinkable groups, and
(iii) a polyfunctional material capable of reacting with aminoplast crosslinking agents.
This invention is also a crosslinker/catalyst combination suitable for admixture with an aminoplast crosslinkable resin. The crosslinker/catalyst combination comprises:
(a) a sulfonimide cure catalyst, and
(b) an aminoplast crosslinking agent.
This invention is also a catalyst/polyfunctional material combination suitable for admixture with aminoplast resins, said combination comprising:
(a) a sulfonimide cure catalyst, and
(b) a polyfunctional material capable of reacting with aminoplast crosslinking agents.
This invention is also an improved method of coating substrates by applying to said substrates the curable coating compositions of the invention.
This invention is also a crosslinked article or coating formed from heat-activating the curable compositions of the invention.
DETAILED DESCRIPTION OF THE INVENTION
CURABLE COATING COMPOSITIONS
The curable composition of this invention comprises:
(i) a sulfonimide cure catalyst of this invention,
(ii) a crosslinkingly effective amount of an aminoplast crosslinking agent containing at least 2 crosslinkable groups,
(iii) a polyfunctional material capable of reacting with aminoplast crosslinking agents,
(iv) optional ingredients.
SULFONIMIDE CURE CATALYSTS
The novel cure-catalysts of this invention are represented by the Formula:
RSO.sub.2 NZSO.sub.2 R
wherein each of the R groups is, independently:
(1) a linear, branched, cyclic alkyl, fluoroalkyl, N,N-dialkylamino group of 1 to 20 carbon atoms, or mixtures thereof; or
(2) an aryl group of 1 to 20 carbon atoms containing 5 or less aromatic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups are the same or different groups selected from a group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkyl aminocarbonyl, and N,N-dialkylaminocarbonyl groups; or
(3) an aralkyl group wherein the alkyl and the aryl groups have the same meaning as the alkyl and aryl groups (1) and (2) above; and
wherein the Z group of the formula is:
(4) hydrogen,
(5) acyl, or
(6) an alkyl or an aralkyl group of 1 to 20 carbon atoms inclusive of sulfonimides as described in DeChristopher, P. J., et. al., J. Amer. Chem. Soc., Vol. 91 (9), p. 2384 (1969) and Curtis, V. A., et. al., Tetrahedron Lett., Vol. 12, p. 199 (1981).
Alkyl or aralkyl groups of (6) which are preferred as the substituent Z are those containing at least one hydrogen at the position beta to the point of attachment of the alkyl group to the nitrogen of the sulfonimide such that upon nucleophilic deacylation reaction of the acylated sulfonimide or upon heat-activated or base-catalyzed elimination or nucleophilic displacement reaction of the alkylated sulfonimide, an unsubstituted sulfonimide is obtained which sulfonimide is represented by the following formula:
RSO.sub.2 NHSO.sub.2 R
Particularly useful are the sulfonimide cure-catalysts containing both alkyl and aryl groups such as the ortho- meta- and para-isomers of methyl tolyl sulfonimide, or mixtures thereof, the para isomer being preferred, and represented by the formula: ##STR1## wherein the alkyl group imparts solubility and the aryl group contributes to the higher melting point. This combination of substituents produces a solid cure catalyst which is well suited to powder coatings applications.
Diarylsulfonimides are similarly well suited for powder coatings applications because of their higher melting point. Particularly useful in this invention are the para-substituted diarylsulfonimide, having Formula: ##STR2## wherein X is selected from a group consisting of hydrogen, chloro, methyl, nitro, alkyl, amino, cyano, alkoxycarbonyl, carboxyl, acyl, N-alkylaminocarbonyl, and N,N-dialkylaminocarbonyl groups. In the above substituted diarylsulfonimide structure each X may also be substituted in the ortho- or meta-position.
Sulfonimides containing a plurality of imide groups are also usable as catalysts in the compositions of this invention, and can be of two types:
1. Linear polyfunctional sulfonimides, represented by the formula: ##STR3## wherein n groups of the .paren open-st.R--SO.sub.2 NH--SO.sub.2 .paren close-st. units may be the same or different, and the R group in each of the n units is independently selected from the group consisting of:
a. a linear, branched, or cyclic or fluoroalkylene group of 1 to 20 carbon atoms; or
b. an arylene group of 1 to 20 carbon atoms containing 5 or less carbocyclic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups are the same or different groups selected from a group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkylaminocarbonyl, and N,N-dialkylaminocarbonyl groups; or
c. an aralkylene group wherein the alkylene and the arylene groups have the same meaning as the alkylene and arylene groups (a) and (b) above; and wherein n is 2 or greater; and
2. Pendant polyfunctional sulfonimides, represented by the Formula: ##STR4## wherein P is either a polyfunctional group or a polymer backbone of a molecular weight greater than 500, and R is an alkyl or aryl group of 1 to 20 carbon atoms, and n is 2 or greater.
The amine salts of the sulfonimides of this invention are also usable as latent-reactive cure catalysts in the compositions of this invention. They are represented by the formula: ##STR5## wherein the R groups are, independently: a. a linear, branched, or cyclic alkyl, or fluoroalkyl group of 1 to about 10 carbon atoms, or mixture thereof; or
b. an aryl group of 1 to 20 carbon atoms containing 5 or less carbocyclic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups are the same or different groups selected from a group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkozycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkylaminocarbonyl, and N,N-dialkylaminocarbonyl groups, or
c. an aralkyl group wherein the alkyl and the aryl groups have the same meaning as the alkyl and aryl groups in (a) and (b) above.
One, two, or all three R groups of the amine part of the sulfonimide salts can be replaced with one, two or three hydrogen atoms to give secondary ammonium, primary ammonium, or ammonium salts, respectively. Like tertiary amine salts, these are usable in the compositions of the invention as latent-reactive cure catalysts.
The R group in the amine salts above can further be independently interrupted and substituted wtih heteroatoms or heteroatom-containing groups to produce amine salts such as those derived from N,N-dimethylethanolamine, triethanolamine, morpholine, 2-amino-2-methyl-1-propanol, N,N-dimethyl ethanolamine, N-methyl diethanolamine, ethanolamine, diethanolamine, and the like.
The preferred amine salts of the invention are derived from relatively low molecular weight amines which are sufficiently volatile to facilitate the expulsion of the free amines from the cured coatings either before or during the curing process.
Exmples of the volatile amines are triethanolamine, diisopropylamine, triisopropylamine, in addition to the hoteroatom-containing amines recited above.
The sulfonimide cure catalyst of this invention may take a latent reactive form such as an N-sulfonyl-substituted saccharin which is later reacted with a nucleophile such as ammonia, primary or secondary alcohols, mercaptans, or amines. For example: ##STR6## where, R is an alkyl or aryl group such as shown in the reference: Imai, Y. et. a., Nippon Kagaku Kaishi, No. 1, p. 111 (1982).
The molecular weight of the sulfonimide cure catalyst used in the crosslinker/catalyst ingredient is preferably high enough to make the sulfonimide catalyst a solid at ambient temperatures, and more preferably a solid at above ambient temperatures (viz., about 40.degree. C.) such as those which may be encountered in commercial in-plant storage or transportation environments.
The sulfonimide catalysts are generally prepared by the reaction of sulfonyl chlorides with a sulfonamide in the presence of a base. Typical preparatory methods are taught in U.S. Pat. Nos. 3,052,656 and 4,510,324, Federal Republic of Germany Patent Nos. 765,789, 1,265,157 and 1,235,300, and DDR Patent No. 9,132.
CROSSLINKING AGENTS
Crosslinking agents of this invention are aminoplast crosslinkers commonly used in coatings, mouldings, and adhesives. The term "aminoplast" is defined herein as a class of resins prepared by the reaction of an amino group-containing compound and an aldehyde.
The reaction product of amino group-containing compounds and aldehydes is often reacted further with an alcohol to produce partially or fully alkylated derivatives. These derivatives are included in the "aminoplast" definition given above.
The term "aminoplast" as used in the context of this invention also includes phenoplasts (phenolic resins), specifically, the resole-type resins which are the reaction product of phenol and an aldehyde and have the further property of containing pendant hydroxymethyl or alkoxymethyl groups. Resole resins and resolated Novolak resins are examples of phenoplasts suitable as crosslinking agents (see, Kirk-Othmer, "Encyclopedia of Chemical Technology", Vol. 17, 3'd Edition, pages 384-390 (1985) and "Encyclopedia of Polymer Science and Engineering", Vol. 11, 2'd Edition, edited by Mark, Bikales, overberger, and Menges, (1985) pages 45-57. Commercially avaiable phenoplasts are Bakelite.RTM. Phenolic Baking Resins sold by Union Carbide Company, Danbury, Conn., (USA).
In the preparation of aminoplasts from amino group-containing compounds and aldehydes and subsequent alkylation, dimeric and oligomeric products resulting from self-condensation reaction are often obtained. These oligomeric self-condensation products are also included in the "aminoplast" definition given above.
The aminoplast crosslinking agents of this invention are represented by the formula:
A--(R).sub.n
wherein the A group in A--(R).sub.n is an n-functional polyamino anchor molecule connected to n(R) groups via the nitrogens and includes the following systems represented by the formulae: ##STR7## wherein R.sup.1 and R.sup.2 are independently, hydrogen, alkyl or aryl groups of 1 to 10 carbon atoms; ##STR8## wherein R.sup.3 is an aliphatic or cycloaliphatic alkyl group, of 1 to 10 carbon atoms, such as methyl, ethyl, butyl, cyclohexyl and the like; or
R.sup.3 is an aromatic group, of 1 to 10 carbon atoms, such as phenyl, tolyl, naphthyl, and the like; or
R.sup.3 is an aralkyl group, of 1 to 10 carbon atoms, such as benzyl, cumyl, and the like; ##STR9## wherein R is an alkylone or an arylene of 1 to 10 carbon atoms; ##STR10## (i) homopolymers containing acrylamide units of the formula: ##STR11## wherein R is hydrogen or alkyl and m is greater than 2, and copolymers thereof;
(j) polycarbamates;
(k) polyhydantoins;
(l) polyamides;
(m) dialkozyethylene ureas;
(n) dihydroxyethylene urea represented by the formula: ##STR12## (o) homopolymers containing carbamate units of the formula: ##STR13## wherein R is hydrogen or alkyl, and m is greater than 2, and copolymers thereof;
(p) miztures of any of (a) through (o); and
wherein the R group in A--(R).sub.n is hydrogen, or an alkyl group of 1 to about 10 carbon atoms, or a crosslinkable group such as --CH.sub.2 OH and --CH.sub.2 OR.sup.4 wherein R.sup.4 is an alkyl group of 1 to about 10 carbon atoms or an aminoplast group-containing oligomeric group provided that the total number of the crosslinkable groups per each aminoplast crosslinking agent is at least 2, and preferably more than 2; and
wherein n in A--(R).sub.n is the total functionality of the polyamino anchor molecule A, and is 2 or greater.
The preferred crosslinking agents of this invention are substantially fully etherified, substantially fully methylolated, substantially monomeric aminoplast crosslinkers commonly used in coatings industry. They are characterized by having at least 2, preferably more than 2 crosslinkable groups per crosslinker molecule. It is well known in the art that the minimum number of crosslinkable functional groups required to effect crosslinking is 2 provided that the aminoplast-reactive polyfunctional material has more than 2 functional groups per each molecule. If, on the other hand, the aminoplast-reactive polyfunctional material has only 2 functional groups per each molecule, then each aminoplast crosslinking agent is required to have more than two crosslinkable groups per crosslinker molecule to be capable of producing a crosslinked network.
The most preferred aminoplast crosslinking agents of the invention are selected from a group consisting of substantially fully etherified, substantially fully methylolated, substantially monomeric glycoluril, melamine, benzoguanamine, cyclohexanecarboguanamine, urea, substituted linear and cyclic ureas, and mixtures thereof.
In addition to the substantially fully etherified, substantially monomeric amine-aldehyde aminoplast crosslinking agents described above, the non-etherified or partially etherified substantially fully methylolated or partially methylolated monomeric and oligomeric aminoplasts are also usable in the compositions of this invention. The unetherified or partially etherified aminoplasts generally cure faster than the fully methylolated and etherified aminoplasts in the presence of weaker acid catalyst and may be used advantageously in such cases.
Glycoluril Crosslinkers
The most preferred glycoluril crosslinkers of this invention are N-substituted glycolurils represented by the formula: ##STR14## wherein at least two of the R groups are selected from a group consisting of methoxymethyl, ethoxymethyl, propoxymethyl, butoxymethyl, pentozymethyl, hexoxymethyl, heptoxymethyl, octoxymethyl, nonoxymethyl, decoxymethyl and mixtures thereof, and the remaining R groups are selected from hydrogen, alkyl, hydroxymethyl, and glycoluril group-containing oligomeric moieties.
While it is preferable to have 4 alkoxymethyl groups per each glycoluril crosslinking agent, under ordinary circumstances it may not be necessary to obtain the pure tetrasubstituted monomeric crosslinker N,N',N",N'"-tetraalkoxymethylglycoluril represented by formula: ##STR15## wherein R is an alkyl group of 1 to about 10 carbon atoms.
The monomeric tetraalkozyglycolurils themselves are not considered to be resinous materials since they are, as individual entities, non-polymeric compounds. They are considered, however, to be potential resin-forming compounds when subjected to heat, and particularly when subjected to heat under acidic conditions. As a result of the described resin-forming ability, the substantially monomeric glycoluril crosslinkiers-of this invention may contain some higher oligomeric components such as dimers, trimers, and tetramers. The presence of modest amounts of these oligomeric forms is permissible and indeed beneficial in cases where a high melting solid crosslinker is desirable as it is the case in powder coatings.
An example of glycoluril crosslinker of this invention is POWDERLINK.RTM. 1174 Powder Crosslinking Agent, a product of American Cyanamid company, Wayne, N.J., and has the following properties:
______________________________________ ##STR16##
______________________________________Non Volatiles, mininum 98(% by weight)Appearance White to pale yellow granulated flakesMelting Point (.degree.C.) 90-110.degree. C.Average Molecular Weight 350Equivalent Weight 90-125______________________________________
Another example of a glycoluril crosslinker of this invention is CYMEL.RTM. 1170 fully butylated glycoluril crosslinker, a product of American Cyanamid Company, Wayne, N.J., having the following properties:
______________________________________Non Volatiles, minimum 95(% by weight)Appearance Clear liquidColor, Maximum (Gardner 1963) 3Viscosity (Gradner-Holt, 25.degree. C.) X-Z.sub.2Molecular Weight, Average 550Equivalent Weight 150-230Methylol Content Very low______________________________________
Urea Crosslinkers
An example of a urea crosslinker usable in this invention is BEETLE.RTM. 80 butylated urea-formaldehyde resin, a product of American Cyanamid Company, Wayne, N.J., having the following properties:
______________________________________Appearance Clear LiquidColor, Maximum (Gardner 1963) 1Non-Volatiles (Weight %)* 96 .+-. 2Viscosity (Gardner-Holt, 25.degree. C.) X-Z.sub.3Solvent Tolerance (ASTM D1198-55) >500______________________________________ *Foil Method (45.degree. C./45 min.).
Melamine Crosslinkers
The melamine-based aminoplast crosslinking agents are well known in the art and have been used extensively as effective crosslinkers in coatings.
Unlike the tetrafunctional glycolurils, alkoxymethylmelamine functionality can be a maximum of six in a crosslinkingly effective range of 2 to 6 alkoxymethyl groups per each melamine molecule.
Like the glycolurils, alkoxymethyl melamines can contain dimers, trimers, tetramers, and higher oligomers, each given combination of monomers and oligomers being preferred for a given application. For example, the lover viscosity monomer-rich compositions are preferred for solvent-based high solids coatings.
An example of the substantially fully etherified, substantially fully methylolated, substantially monomeric melamines usable in this invention is CYMEL.RTM. 303 melamine crosslinking agent, a product of American Cyanamid Company, Wayne, N.J., and has the following properties:
______________________________________ ##STR17##
______________________________________Non-Volatiles (% by weight)* 98Color, Maximum (Gardner 1963) 1Viscosity (Gardner-Holt, at 25.degree. C.) X-Z.sub.2Free Formaldehyde, maximum (weight %) 0.5Degree of Polymerization 1.75______________________________________ *Foil Method (45.degree. C./45 min).
Another example of the substantially fully etherified, substantially fully methylolated, substantially monomeric melamines is CYMEL.RTM. 1168 melamine crosslinking agent, a product of American Cyanamid company, Wayne, N.J. The alkyl group in CYMEL.RTM. 1168 consists essentially of a mixture of methyl and isobutyl groups. It has the following properties:
______________________________________ ##STR18##
______________________________________Non-Volatiles (% by weight)* 98Color, maximum (Gardner 1963) 1Free Formaldehyde, maximum (weight %) 0.5Viscosity (Gardner-Holt, at 25.degree. C.) X-Z.sub.2Equivalent weight 150-230______________________________________ *Foil Method (45.degree. C./45 min).
An example of a substantially methylolated, partially etherified, substantially oligomeric melamine is CYMEL.RTM. 370 crosslinking agent, a product of American Cyanamid company, Wayne, N.J. It has the following properties:
______________________________________Non-Voltailes (% by weight)* 88 .+-. 2Solvent IsobutanolViscosity (Gardner-Holt, at 25.degree. C.) Z.sub.2 -Z.sub.4Color, maximum (Gardner 1963) 1Equivalent Weight 225-325______________________________________ *Foil Method (45.degree. C./45 min)
Guanamine Crosslinkers
As in melamines, the partially or fully methylolated or etherified alkyl and aryl guanamine aminoplasts, both in their monomeric and oligomeric forms, are usable as crosslinking agents in this invention, with the selection depending on the particular application or the properties desired in the product.
Benzoguanamine, cyclohexylcarboguanamine and acetoguanamine aminoplasts are especially preferred as crosslinkers in this invention. The benzoguanamine crosslinkers are represented by the formula: ##STR19## wherein R is an alkyl group of 1 to about 10 carbon atoms, or a mixture thereof. An example of a benzoguanamine-based crosslinking agent is CYNEL.RTM. 1123 Resin as described above, and wherein R is a mixture of methyl and ethyl groups.
The acetoguanamine-based crosslinkers are represented by the formula: ##STR20## wherein each R is independently an alkyl group of 1 to about 10 carbon atoms.
The cyclohexylcarboguanamine-based crosslinkers are represented by the formula: ##STR21## wherein each of the R groups is independently an alkyl group of 1 to about 10 carbon atoms, or a mixture thereof.
It is evident from the discussions above, that a person skilled in the art, in selecting the most suitable crosslinker for a particular application, may choose a mixture thereof which imparts a balance of properties desired for that particular application.
RATIO AND PROPORTIONS OF INGREDIENTS
The aminoplast crosslinking agent (ii) is combined with the polyfunctional aminoplast-reactive ingredient (iii) in proportions that give weight ratio of the ingredients (ii):(iii) ranging from about 1:40 to about 3:1.
The weight ratio of the sulfonimide catalyst (i) to the aminoplast crosslinking agent (ii) is from about 1:4 to about 1:400.
The effective concentration of the sulfonimide cure catalyst is from about 0.01 to about 10 weight percent based on the total weight of resin solids. It is preferably from 0.3 to 0.8 weight percent of the total resin solids.
OPTIONAL INGREDIENTS
The optional ingredients present in the curable composition of the invention vary depending on the intended use of the cured article or film.
Suitable optional ingredients include fillers, ultraviolet light stabilizers, pigments, flow control agent, plasticizers, mold release agents, and corrosion inhibitors.
The composition of the invention may contain as an optional ingredient a liquid medium. Such a medium may be used to aid the uniform application and transport of the curable composition. Any or all of the ingredients of the composition may be contacted with the liquid medium. Moreover, the liquid medium may permit formation of a dispersion, emulsion, invert emulsion, or solution of the curable composition ingredients. Particularly preferred is a liquid medium which is a solvent for the curable composition ingredients (i), (ii), and (iii). Suitable solvents are selected from alcohols, ketones, ethers, esters, water, aliphatic hydrocarbons, aromatic hydrocarbons, halogenated hydrocarbons and mixtures thereof.
POWDER COATING COMPOSITION
The novel curable powder coating composition of this invention comprises:
(i) a sulfonimide cure catalyst of this invention,
(ii) a polyfunctional material capable of reacting with aminoplast crosslinking agents,
(iii) a crosslinkingly effective amount of a aminoplast crosslinking agent containing at least 2 crosslinkable groups,
(iv) optional ingredients.
It is necessary that at least one of the powder coating ingredients (i), (ii), (iii) or (iv) be a solid, with the proviso that the solid ingredient(s) of the powder coating composition be capable of retaining the non-solid ingredient(s) to give a composition that as a whole is a solid.
A much preferred embodiment of the invention is a composition wherein the powder coating ingredients (i), (ii), (iii), and (iv) are all solids having the form of a flowable powder.
In recent years, powder coating technology has been the subject of considerable interest and commercial growth. Because powder coatings are all solids systems, they do not suffer from the solvent-related disadvantages of the solvent-based coatings systems. Powder coating minimizes the cost of shipping, storing, handling, and solvent waste disposal.
In powder coatings the ingredients used are essentially similar to conventional liquid coatings except that the powder coating composition is required to be a solid.
Preferred Powder Coating Compositions:
Preferred powder coating compositions are those wherein the ingredients (i), (ii), (iii) and (iv) are all solids. More particularly, the individual composition ingredients are as described below:
(i) The novel sulfonimide cure catalysts usable in powder coatings are the sulfonimides of this invention having melting points ranging from about 40.degree. C. to about 250.degree. C., and more preferably ranging from about 80.degree. C. to about 180.degree. C.
(ii) The polyfunctional materials usable in powder coatings are the polyfunctional materials of this invention having a glass transitions (Tg) ranging from about 40.degree. C. to about 150.degree. C., and softening points ranging from about 40.degree. C. to about 150.degree. C., and more preferably ranging from about 80.degree. C. to about 140.degree. C.
It is preferable that the powder coating composition as a whole be a solid at ambient temperatures and that it remains solid up to about 40.degree. C. to preserve the powdery state of the curable composition and to prevent lumping.
Upon heating, however, these resins should become fluid to permit formation of low viscosity melts which allow efficient mixing of the components of the curable composition prior to crosslinking. It is desirable that the aminoplast-reactive resins become fluid at temperatures ranging from about 80.degree. C. to about 150.degree. C., and most preferably from about 100.degree. C. to about 140.degree. C.
(iii) The aminoplast crosslinking agents usable in powder coatings are the solid aminoplast crosslinking agents of this invention having melting or softening points ranging from about 40.degree. C. to about 150.degree. C., and more preferably from about 80.degree. C. to about 140.degree. C., and most preferably from about 100.degree. C. to about 120.degree. C.
Glycoluril type aminoplast crosslinking agents are particularly preferred because they are solids at ambient temperatures and generally have suitable melting points.
It is preferable that the solid aminoplast crosslinking agents are solids at ambient temperatures and that they remain solids up to about 40.degree. C. to preserve the powdery state of the curable composition and to prevent lumping. It is desirable that the aminoplast crosslinking agents become fluid at temperatures ranging from about 80.degree. C. to about 150.degree. C., and more preferably from 100.degree. C. to about 140.degree. C.
(iv) The curable powder coating compositions may include varying amounts of optional ingredients such as benzoin at about 1 to 4 weight percent level. The composition may also include as a flow control agent ingredients such as Modaflow.RTM. Powder III Resin Modifier, a product of Monsanto Company, or Resiflow P-67 Flow Control Agent, a product or Estron Chemical, Inc. at about 1 to 2 weight percent level. Moreover, fillers and pigments such as titanium dioxide based pigments may be conventionally added to improve the appearance and properties of the coatings and articles formed from the compositions.
POLYFUNCTIONAL MATERIALS
The polyfunctional material capable of reacting with an aminoplast crosslinking agent is one of three essential components required for the curable compositions of this invention. The other essential components are aminoplast crosslinking agents such as N,N',N",N'"-tetramethoxymethylglycoluril, and sulfonimide cure catalyst such as N-(methanesulfonyl)-p-toluenesulfonamide. The aminoplast-reactive functional groups of the polyfunctional material react, under cure conditions, with crosslinkable groups to produce a three dimensional crosslinked network such as those found in coatings, moulded articles and adhesives.
The aminoplast reactive functional groups are selected from a group comprising: amino groups, amido groups, carboxyl groups, mercapto groups, hydroxy groups, and combinations of any of the aforementioned functional groups. Reactive materials having a plurality of carboxy and/or hydroxy groups are particularly preferred in the practice of the invention.
Suitable polyfunctional hydroxy reactant materials may be epoxy or polyurethane prepolymers, alkyds, acrylic resins containing pendant or terminal carboxy or hydroxy functionalities, or polyester resins with pendant or terminal hydroxy or carboxy groups. These are described in greater detail below.
In cases where resins used in the formulations of this invention are intended for powder coating applications, the resins should be solids at ambient temperatures and should remain solids up to about 40.degree. C. to preserve the powdery state of the curable composition and prevent lumping. The aminoplast-reactive materials or resins used in the compositions of the invention preferably have a molecular weight of from about 100 to about 50,000. In the event that the aminoplast reactive material is in the form of an emulsion the molecular weight may be as high as about 5,000,000.
1. ACRYLIC RESIN AMINOPLAST-REACTIVE MATERIAL
The hydroxyfunctional acrylic resins used in formulating the curable compositions of this invention preferably have molecular weights in the range of from about 500 to about 50,000 and hydroxyl group equivalent weights of from about 200 to 4,000. An example of a suitable acrylic resin is JONCRYL.RTM. SCX-800 A acrylic resin, a product of S. C. Johnson and Sons, Inc., having the following physical and chemical properties:
______________________________________Non-Volatiles (weight %) 98Hydroxyl Number 43Equivalent Weight 1300Softening Point (.degree.C.) 100Glass Transition 43Temperature (Tg) (.degree.C.)Acid Value (mg KOH/g) 15ICI Viscosity 25(200.degree. C., Poise)______________________________________
Another example of a suitable acrylic resin is JONCRYL.RTM. SCX-800 B acrylic resin, a product of S. C. Johnson and Sons, Inc., having the following physical and chemical properties:
______________________________________Non-Volatiles (weight %) >97Hydroxyl Number 40Glass Transition 43Temperature (Tg) (.degree.C.)Acid Value 15-20Softening Point (.degree.C.) 107Equivalent Weight 1402ICI Viscosity 45-50(200.degree. C., Poise)______________________________________
or JONCRYL.RTM. 500 acrylic resin, a product of S. C. Johnson and Sons, Inc., having the following properties:
______________________________________Viscosity (centipoise) 4000Solids Content (%) 80Hyroxyl Number (based on solids) 140Equivalent Weight (based on solids) 400Molecular Weight (Mn)* 1300Polydispersity (Mw/Mn)** 1.7______________________________________ *Mn = Number Average Molecular Weight. **Mw = Weight Average Molecular Weight.
Commercially available acrylic resins are generally applicable for use in preparing the compositions of the invention. Selection of the optimum acrylic resin will depend an the user's desire to impart to the final cured product particular physical properties such as hardness, flexure, chemical and solvent resistance, and etc.
2. POLYESTER RESINS
The hydroxy functional polyester resins used in formulating the curable compositions of this invention preferably have molecular weights in the range of from about 1,000 to 50,000 and hydroxyl group equivalent weights of from about 200 to 4,000.
An example of a suitable polyester resin is Arakote.RTM. 3109 solid hydroxyl terminated polyester powder coating resin, a product of Ciba-Geigy Corporation, Hawthorne, N.Y., having the following physical and chemical properties:
______________________________________Color Colorless SolidOH Number 27-32ICI Viscosity at 200.degree. C. (Poise) 40Glass Transition Temperature 66(Tg) (.degree.C.)Equivalent Weight 1900______________________________________
Another example of a suitable polyester resin is ALPTALAT.RTM. AN 745 hydroxyfunctional polyester resin, a product of Hoechst Corporation, having the following physical and chemical properties:
______________________________________Color, 50% (ASTM D 1544-68) 3OH Number 30Equivalent Weight 1870Acid Value (mg KOH/g) 8Glass Transition 55Temperature (Tg) (.degree.C.)ICI Viscosity (200.degree. C., Poise) 50-65______________________________________
Another example of a suitable polyester resin is ARAKOTE.RTM. 3010 carboxyl-terminated polyester, a product of Ciba-Geigy Corporation, Ardsley, N.Y., having the following properties:
______________________________________Color, Maximum (Gardner, ASTM D 2849) 2OH Number .ltoreq.7Acid Value (mg KOH/g) 27-33ICI Viscosity (200.degree. C., Poise) 35-60Glass Transition Temperature (Tg) (.degree.C.) 62Equivalent Weight 1800______________________________________
Another example of a suitable polyester resin is RUCOTE.RTM. 101 polyester resin, a product of Ruco Polymer Corporation, Hicksville, N.Y., having the following physical and chemical properties:
______________________________________Appearance granular solidSoftening Temperature (.degree.C.) 120OH Number 29Acid Value (mg KOH/g) 1Glass Transition Temperature 53(Tg) (.degree.C.)Equivalent Weight 2000ICI Viscosity (200.degree. C., Poise) 53______________________________________
+Another example of a suitable polyester resin is CARGILL 3000 polyester, a product of Cargill Corporation, having the following physical and chemical properties:
______________________________________OH Number 50Equivalent Weight 1035Glass Transition 56Temperature (Tg) (.degree.C.)Acid Value (mg KOH/g) 15______________________________________
Upon cure, polyester resins give films of superior properties, as described in detail in the Examples. A wide variety of commercial polyester resins may be used for the aminoplast-reactive ingredient of the invention, provided such resins have the physical properties suitable for the intended application.
3. OTHER AMINOPLAST-REACTIVE SYSTEMS
Other polyhydroxy functional compounds which are useful in the practice of the invention are diols, triols, tetraols, and higher polyhydroxy alcohols. Illustrative polyhydric alcohols are pentaerythritol dipentaaerythritol, tripentaerythritol, trimethylolethane, trimethylolpropane, anhydroenneahepititol, 1,2,4-butanetriol, and 1,2,6-hexanetriol. These polyols can also be used to totally or partially replace the acrylic resin or polyester resin aminoplast-reactive ingredient of the composition of the invention. However, the film properties resulting from addition of such non-resinous ingredients sometimes are inferior and lack flexibility in the cured film final product.
Polyfunctional epoxy prepolymers, alkyds, and polyurethane prepolymers are also usable as hydroxyfunctional aminoplast-reactive materials.
Polyfunctional amides are also suitable as aminoplast-reactive components, provided they have the proper physical properties suitable for the intended use. For example, for powder coatings application, they are solids at up to about 40.degree. C. to allow the preparation of storage stable powders containing the aminoplast crosslinking agents. The crosslinked films and articles resulting from polyamide-containing curable compositions, however, have physical properties somewhat different (i.e. harder) than polyester and acrylic-based systems described above.
THE CATALYST/CROSSLINKER COMBINATION
The catalyst/crosslinker combination of the invention is a uniform mixture of the following materials:
(a) a sulfonimide cure catalyst, and
(b) an aminoplast crosslinking agent containing at least two crosslinker groups.
Suitable sulfonimide cure catalysts (a) and aminoplast crosslinking agents (b) are as set out in the preceding sections. The components (a) and (b) can each be either liquids or solids. A particularly preferred catalyst/crosslinker combination is one wherein both the sulfonimide catalyst (a) and the aminoplast crosslinker (b) are both solids at 40.degree. C.
THE IMPROVED METHOD OF COATING BY THIS INVENTION
This invention is also an improved method of coating substrates by applying to substrates the coating composition of the invention.
A Method of Coating Using Liquid Coating Compositions:
This invention is a method of coating substrates using a liquid curable coating composition, where the composition contains the following ingredients:
(i) a sulfonimide cure catalyst,
(ii) a crosslinkingly effective amount of an aminoplast crosslinking agent containing at least 2 crosslinkable groups,
(iii) a polyfunctional material capable of reacting with aminoplast crosslinking agents, and
(iv) a liquid medium.
The liquid curable coating composition of the invention may be contacted with a substrate by spraying, padding, brushing, rollercoating, curtaincoating, flowcoating, electrostatic spraying, electrocoating or dipping.
A Method of Coating Using Powder Coating Compositions:
"Powder coating" is an art recognized process and is defined herein as a method of electrostatic powder spraying wherein a finely divided solid coating material is electrostatically attracted to a surface of an article. Alternatively, the powder coating composition may be contacted with the substrate by immersing the substrate in fluidized bed of powder. The article covered with the powder is heated to at least the fusion temperature of the coating composition forcing it to flow out and form a coating which is cured by further application of heat.
The prior art powder coating process can be considerably improved by using as the coating material a low temperature heat-curable aminoplast coating composition comprising as essential ingredients:
(i) a solid sulfonimide cure catalyst of this invention,
(ii) a solid polyfunctional aminoplast-reactive material, and
(iii) a solid aminoplast crosslinking agent.
The unexpectedly superior properties of the films formed from the powder coating compositions of the invention are their superior appearance manifested in gloss and smoothness, improved impact and corrosion resistance.
A typical procedure for using the compositions of the invention is as follows:
The substrates are coated with the powder coating composition of the invention and subjected to a temperature of from about 90.degree. C. to about 350.degree. C. to melt and spread the composition uniformly onto the substrate surface. Thereafter, the substrate is held at a temperature of from about 120.degree. C. to about 350.degree. C. to crosslink the composition and form the permanently cured coating.
CATALYST/POLYFUNCTIONAL MATERIAL COMBINATION
The catalyst/polyfunctional material combination of the invention is a uniform mixture of the following materials:
(a) a sulfonimide cure catalyst, and
(b) a polyfunctional material capable of reacting with aminoplast crosslinking agents.
Suitable sulfonimide cure catalysts (a) and suitable polyfunctional materials capable of reacting with aminoplast crosslinking agents (b) are set out in the preceding sections.
The components (a) and (b) can each be either liquids or solids. A particularly preferred catalyst/polyfunctional material combination is one wherein the sulfonimide cure catalyst (a) and the polyfunctional material capable of reacting with aminoplast crosslinking agents (b) are both solids at 40.degree. C. In the preferred mode, components (a) and (b) are blended to form a masterbatch, which is then admixed with an aminoplast crosslinking agent. Optionally, the masterbatch is admixed with an aminoplast crosslinking agent and an additional amount of polyfunctional material.
The suitable weight ratio of the catalyst (a) to polyfunctional material (b) is in the range of from about 1:10,000 to about 9:1, with ratios of from about 3:1 to about 1:20 being preferred.
The solid sulfonimide cure catalyst/polyfunctional material combinations of the invention are prepared by a process comprising the steps of:
(a) heating a mixture of a solid sulfonimide cure catalyst and a solid polyfunctional material at a temperature sufficient to produce a uniform melt-mixed resinous material,
(b) cooling said melt-mixed resinous material to a temperature sufficient to produce a solid, and
(c) crushing the solid to produce a powdered sulfonimide cure catalyst/polyfunctional material combination usable in the improved method of powder coating described hereinbelow.
IMPROVED METHOD OF POWDER COATING WITH CATALYST/POLYFUNCTIONAL MATERIAL COMBINATION
An improved method of coating substrates by contacting said substrates with a powder coating composition and thereafter heat curing said composition, wherein the improvement comprises: contacting said substrate with a curable powder coating composition comprising:
(i) a combination of sulfonimide cure catalyst/polyfunctional material capable of reacting with aminoplast crosslinking agents,
(ii) a crosslinkingly effective amount of an aminoplast crosslinking agent containing at least 2 crosslinkable groups,
(iii) optionally, an additional amount of a polyfunctional material capable of reacting with aminoplast crosslinking agents, and
(iv) other optional ingredients known to be usable in powder coatings technology.
The improved method of powder coating employs a preblended mixture of the sulfonimide cure catalyst and the polyfunctional material which mixture is further blended with the remaining ingredients and the resulting powder is applied to substrates to be coated by methods well known in the art as "Powder Coating," defined and briefly described in a preceding section entitled "A Method of Coating Using Powder Coating Compositions."
Suitable sulfonimide cure catalysts, and polyfunctional materials capable of reacting with aminoplast crosslinking agents are set out in the preceding sections. The ratios of the ingredients are further described below.
The sulfonimide cure catalyst/polyfunctional material combinations (i) are those previously described under the same title. In the masterbatch of catalyst/polyfunctional material combination (i), the suitable weight ratio of the sulfonimide cure catalyst to polyfunctional material is in the range of from about 1:10,000 to about 9:1, with a ratio of about 1:1 being preferred. The weight percent of the sulfonimide cure catalyst in the catalyst/polyfunctional material combination of ingredient (i) is from about 0.01 percent to about 90 percent, with 50 weight percent being preferred.
In the curable compositions of the improved method of powder coating, the weight percent of the sulfonimide cure catalyst/polyfunctional material ingredient (i) is in the range of 0.01 to 97.5 percent of the total weight of the resin-forming ingredients, with 1.0 percent being preferred. The weight ratio of the aminoplast crosslinking agent to total polyfunctional material is from about 1:40 to about 3:1, and the weight percent of the sulfonimide cure catalyst is in the range of 0.01 to about 10 weight percent of the total weight of the resin-forming ingredients.
"Resins-forming ingredients " are defined herein as the sum of the total polyfunctional material and the aminoplast crosslinking agent. Other ingredients are excluded from the above definition.
CROSSLINKED ARTICLES AND COATINGS FORMED BY THE COMPOSITIONS OF THIS INVENTION
The curable compositions of this invention containing the sulfonimide cure-catalyst of the invention can be heat cured (typically 90.degree. C. to 400.degree. C.) to produce crosslinked moulded articles, adhesives and coatings. Because of the polyfunctional nature of the reactants, the resulting product in this case is a crosslinked article in the form of a film such as adhesives and/or coatings or the form of an article such as molded products.
The heat-cured compositions of this invention may be employed as coatings for wire, appliances, automotive parts, furniture, pipes, machinery, and the like.
The heat-cured compositions may also be used to form solid articles such as cases, enclosures, and structural members.

The following Examples illustrate various embodiments of the invention.
EXAMPLE 1
PREPARATION OF THE SULFONIMIDE CURB CATALYSTS*
* Prepared by the general procedure described in the following reference article: N. N. Dykhanov, Zhur. Obshchei Khim., 29, 3602 (1959); Chemical Abstracts (54) 19577g (1960).
PART A
p-Toluenesulfonyl chloride (38.2 g, 0.20 mole) was added, in five portions over a period of 90 minutes, to a heated (70.degree. C.) solution of methanesulfonamide (19.0 g, 0.20 mole) in aqueous 5% sodium hydroxide (176 ml). Throughout the addition, a pH of 12 was maintained by frequent additions of aqueous 5% sodium hydroxide solution. After stirring for about 20 hours at about 70.degree. C., the reaction mixture was cooled to room temperature and acidified with concentrated hydrochloric acid to pH less than 1 and extracted with dichloromethane (3.times.200 ml). The organic layer was separated, dried (sodium sulfate) and concentrated to 150 ml. Addition of n-heptane (200 ml) gave highly pure methyl para-tolyl sulfonimide, also known as N-(methanesulfonyl)-p-toluenesulfonamide, a sulfonimide cure catalyst of the invention, as a white precipitate (18.3 g), m.p. 117.degree.-120.degree. C.
Example 1, Part A illustrates the preparation of a mixed aryl and alkyl group containing cure catalyst of this invention.
PART B
The procedure of EXAMPLE 1, PART A was followed with the exception that methanesulfonamide was replaced with an equivalent amount of p-toluenesulfonamide (34.2 g, 0.20 mole) and the extraction step was replaced by a purification step to give the symmetrical di-(p-toluene)sulfonimide, a sulfonimide cure catalyst of the invention, as a white solid of 96% purity, m.p. 171.degree.-173.degree. C.
EXAMPLE 1, PART B illustrates the preparation of the symmetrical di-(p-toluene)sulfonimide, which is another example of the sulfonimide cure catalysts of this invention.
PART C
A commercially available sulfonimide, N-(4-aminobenzenesulfonyl)benzenesulfonamide, a product of Aldrich Chemicals, Milwaukee, Wis., was used as cure catalyst in the preparation of Composition C.
PART D
The procedure of EXAMPLE 1, PART A, was followed with the exception that methanesulfonamide and p-toluenesulfonyl chloride were replaced, respectively, with equivalent amounts of p-nitrobenzenesulfonamide and a solution of p-nitrobenzenesulfonyl chloride in acetone (50 ml). Also, the extraction step was replaced with a purification step to give the symmetrical di-(4-nitrobenzene)sulfonimide, a sulfonimide cure catalyst of the invention, as an off-white solid of 98% purity, m.p. 238.degree.-240.degree. C.
EXAMPLE 1, PART D illustrates the preparation of another example of sulfonimide cure catalyst of this invention.
EXAMPLE 2
This example illustrates the preparation of powder coatings using the sulfonimide cure catalysts of the invention.
The following four curable compositions, Composition A, B, C, and D, were formulated using sulfonimide cure catalysts of this invention and thereafter cured at 190.degree. C. (20 min).
1. PREPARATION OF THE CURABLE COMPOSITIONS
______________________________________ Weight (g)______________________________________A. COMPOSITION A Arakote .RTM. 3109 Polyester (solid) 94.00 Powerlink .RTM. 1174 Crosslinking 6.00 Agent (solid) Sulfonimide Cure Catalyst of Example 1, 0.50 Part A Benzoin (a solid additive) 1.40 R960-48 .RTM. Titanium Dioxide Pigment 40.00 (product of DuPont Company, Wilmington, Delaware) Resiflow P-67 Flow Control Agent 1.30 (product of Estron Chemical, Inc. Culvert City, Ky)B. COMPOSITION B Arakote .RTM. 3109 Polyester (solid) 94.00 Powderlink .RTM. 1174 Crosslinking 6.00 Agent (solid) Sulfonimide Cure Catalyst of Example 1, 0.50 Part B Benzoin (a solid additive) 1.40 R960-48 Titanium Dioxide Pigment 40.00 Resiflow P-67 Flow Control Agent 1.25C. COMPOSITION C Arakote .RTM. 3109 Polyester (solid) 94.00 Powderlink .RTM. 1174 Crosslinking 6.00 Agent (solid) Sulfonimide Cure Catalyst of Example 1, 0.50 Part C Benzoin (a solid additive) 1.40 R960-48 Titanium Dioxide Pigment 40.00 Resiflow P-67 Flow Control Agent 1.25D. COMPOSITION D Arakote .RTM. 3109 Polyester (solid) 94.00 Powderlink .RTM. 1174 Crosslinking 6.00 Agent (solid) Sulfonimide Cure Catalyst of Example 1, 0.50 Part D Benzoin (a solid additive) 1.40 Titanium Dioxide Pigment 40.00 Resiflow P-67 Flow Control Agent 1.25______________________________________
A control composition was prepared as described above in Composition A with the exception that no cure catalyst was used.
All components were dry-blended in a Waring blender or a Welex mixer for small and larger scale runs, respectively. The dry-blended powder was then melt-mixed at about 90.degree. C. to 135.degree. C. for 1-5 minutes in a two roll mill to allow homogeneous mixing without allowing crosslinking to occur. The melt-mixed material was then chopped into smaller pieces in a blender mill or a pelletizer, and fed into a mill classifier where the chips were ground to a fine powder with particle size about 35 microns. The finely ground powder, charged with up to 80 KV power, was then sprayed through an electrostatic spray gun on grounded metal substrates, Bonderite.RTM. 1000 (a product of Parker Industries, Inc.) in a spray booth.
2. CURING THE CURABLE COMPOSITIONS
The electrostatically coated Bonderite 1000 substrates containing the curable compositions of the invention were then baked in an oven at 190.degree. C. to allow the powder to fuse, flow out and crosslink. These processes were analyzed by means of a viscometer and a rheometer.
TABLE 1 summarizes the cure conditions, the film properties resulting from curing the curable compositions and particularly the film appearance.
It is concluded from the results in EXAMPLE 2 that powder coatings prepared by using the curable compositions of this invention which contain the cure catalysts of this invention have excellent film properties and appearance. The control formulation without catalyst did not cure, showing the necessity of catalyst inclusion in the formulation.
TABLE 1______________________________________POWDER COATINGS FROM CURABLE COMPOSITIONSOF THE INVENTIONCURE CONDITIONS, FILM PROPERTIES AND APPEARANCE CURABLE COMPOSITIONS* Comp. Comp. Comp. Comp. A B C D______________________________________CURE CONDITIONSCatalyst of Part A Part B Part C Part DExample 1Weight of 0.50 0.50 0.50 0.50Catalyst (g)Bake Temperature 190 190 190 190(.degree.C.)Bake Time (min.) 20 20 20 20FILM APPEARANCE Orange Orange Orange Orange Peel Peel Peel Peel Micro- Micro- Micro- Micro- blisters blisters blisters blisters Craters Pinholes Gel SeedFILM PROPERTIESFilm Thickness 1.9-2.3 1.9-2.5 1.4-2.4 1.0-2.0(mils)(ASTM D-1400-81)Film Thickness 0.048- 0.048- 0.036- 0.025-(mm) 0.058 0.064 0.061 0.050(ASTM D-1400-81)Hardness, KHN.sub.25 13.0 11.7 10.2 12.2ASTM (D-1474-85)MEK Rubs 200+ 200+ 200+ 200+(Double Rubs)Impact, F/R 160/160 160/160 160/160 160/160in lb)(Front/Reverse)ASTM D-2794-82Color, Tristimulus -0.06 -0.03 0.00 0.02Gloss, 60.degree. 94.1 94.0 94.1 78.4Gloss, 20.degree. 79.4 73.4 79.3 32.5RESISTANCE PROPERTIESHumidity (60.degree. C.) 504 528 504 456Time (hrs)ASTM D 4585-87Appearance No No No DenseAfter Testing Change Change Change Micro- blistersSalt Spray, 1008 1008 1008 1032Time (hrs)ASTM B-117Creepage (mm) 3 0 0 0Appearance** 9 9 9 9after testingASTM D-610______________________________________ *The control composition containing no catalyst did not cure well under the conditions of EXAMPLE 2. The film was removed completely in less than 2 MEK double rubs. **Scale is 1 to 0 where 10 is the best.
EXAMPLE 3
The experiments of EXAMPLE 2 were repeated with Compositions A, B, C, and D at the slightly lower temperature of 175.degree. C. Composition C did not cure well. The cure conditions, film properties and film appearance of the remaining compositions are summarized in TABLE 2.
It is concluded from the results in TABLE 2 that the curable compositions of this invention containing the sulfonimide cure catalysts are capable of curing at low temperatures (175.degree. C.) to produce powder coatings with excellent film properties and acceptable appearance.
TABLE 2______________________________________Powder Coatings from Curable Compositionsof the Invention CURABLE COMPOSITIONS Comp. Comp. Comp. A B D______________________________________FILM APPEARANCE Orange Orange Orange Peel Peel Peel Micro- Micro- Micro- blisters blisters blisters CratersFILM PROPERTIESFilm Thickness 1.8-2.8 2.5-3.5 1.5-2.5(mils)Film Thickness 0.046-0.071 0.064-0.089 0.038-0.064(mm)Hardness KHN.sub.25 11.8 12.7 10.5MEK Rubs 20/200+ 10/200+ 200+Impact F/R (in-lb) 160/160 100-120/0-20 160/160Color, Tristimulus -0.06 -0.03 0.05Gloss, 60.degree. 67.4 68.3 58.9Gloss, 20.degree. 47.3 38.3 24.5RESISTANCEPROPERTIESHumidity (60.degree.C.), 456 288 192Time (hrs) Increased Increased IncreasedAppearance Microblis- Micro- Micro-after testing ters, some blisters blisters loss of glossSalt spray, 1008 1008 1008Time (hrs)Creepage (mm) 2 0 0Appearance 9 9 9(after testing)______________________________________
EXAMPLE 4
COMPARATIVE
Curable compositions E, F, and G were prepared and cured at 190.degree. C./20 min. by the method described in EXAMPLE 2.
______________________________________ Weight (g)______________________________________COMPOSITION EArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)Sulfonimide cure catalyut of EXAMPLE 1, 0.30PART ABenzoin (a solid additive) 1.40R960-48 titanium dioxide pigment 40.00Resiflow P-67 flow control agent 1.30COMPOSITION FArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)p-Tolueneaulfonic Acid Monohydrate (solid) 0.30Benzoin (a solid additive) 1.40OR 650 titanium dioxide pigment 40.00Resiflow P-67 flow control agent 1.25COMPOSITION GArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)p-Toluenesulfonic acid monohydrate (solid) 0.20Benzoin (a solid additive) 1.40R960 48 titanium dioxide pigment 40.00Modaflow III flow control agent 1.25______________________________________
TABLE 3 summarizes the film properties and appearance characteristics of the cured coatings obtained by curing the compositions E, F, and G.
It is concluded from the results in EXAMPLE 4 that the curable composition E of this invention containing the sulfonimide cure catalyst of EXAMPLE 1, PART A produces superior powder coatings when compared with curable compositions of the prior art such as compositions F and G containing p-toluenesulfonic acid catalyst commonly used in prior art. The prior art p-toluenesulfonic acid cured system gave unacceptable appearance, lower gloss, and failed in the salt spray test.
TABLE 3__________________________________________________________________________Comparison of Sulfonimide Cure Catalyst with p-Toluenesulfonic Acid inPowder Coatings CURABLE COMPOSITIONS Comp. Comp. Comp. Comp. Comp. E.sup.1 F.sup.2 G.sup.3 F.sup.4 G.sup.4__________________________________________________________________________FILM APPEARANCE Orange Peel Orange Peel Orange Peel Orange Peel Orange Peel Microblisters Microblisters Microblisters Microblisters Microblisters Pinholes Matted Craters Pinholes Gel Seeds Gel Seed Craters Gel SeedFILM PROPERTIESFilm Thickness 2.4-2.9 1.7-3.0 1.9-2.2 1.9-3.3 2.4-3.3(mils)Film Thickness 0.061-0.074 0.043-0.076 0.048-0.056 0.048-0.084 0.061-0.084(mm)Hardness KHN.sub.25 12.1 12.0 10.8 10.6 10.1MEK Rubs 20/200+ 200+ 200+ 200+ 200+Impact F/R (in-lb) 160/160 160/160 45-50/45-50 60-80/80-100 140-160/40-60Color, Tristim- -0.06 0.01 -0.05 -0.03 -0.02ulusGloss, 60.degree. 92.7 83.7 70.3 88.3 86.5Gloss, 20.degree. 78.6 42.9 25.0 48.1 48.5RESISTANCE PROPERTIESHumidity (60.degree. C.), 456 504 120Time (hrs) Increased IncreasedAppearanae Microblisters, No change Microblisters(after testing) slight loss of glossSalt Spray, 1008 768 192Time (hrs)Creepage (mm) 1 3 0Appearance 9(after testing)__________________________________________________________________________ .sup.1 0.3% N(Methanesulfonyl)-1-toluenesulfonamide cure catalyst, based on weight of resin solids. .sup.2 0.3% pToluenesulfonic acid monohydrate cure catalyst, based on weight of resin solids. .sup.3 0.2% pToluenesulfonic acid monohydrate cure catalyst, based on weight of resin solids. .sup.4 Repeat experiments.
EXAMPLE 5
Curable composition H was prepared by the method described in EXAMPLE 2. It was cured at 175.degree. and 190.degree. C. by the method described in EXAMPLE 2.
______________________________________ Weight (g)______________________________________COMPOSITION HAlftalat .RTM. AN 745 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)Sulfonimide cure catalyst of EXAMPLE 1, 0.50PART ABenzoin (a solid additive) 2.40R960-48 titanium dioxide pigment 40.00Resiflow III flow control agent 1.30______________________________________
TABLE 4 summarizes the film properties and appearance characteristics of the cured coatings obtained by curing composition H.
This example illustrates that a sulfonimide cure catalyst of the invention produces excellent powder coating with Alftalat.RTM. AN 745 as well as Arakote.RTM. 3109 polyesters at two different temperatures.
TABLE 4______________________________________Powder Coatings with Alftalat .RTM. AN 745 andPowderlink .RTM. 1174 Cured with a Sulfonimide Cure Catalyst CURABLE COMPOSITION H 175.degree. C. Cure 190.degree. C. Cure______________________________________FILM APPEARANCE Orange Peel Orange Peel Microblisters MicroblistersFILM PROPERTIESFilm Thickness 2.3-2.8 2.1-2.5(mils)Film Thickness 0.058-0.071 0.053-0.064(mm)Hardness, KHN.sub.25 10.9 10.5MEK Rubs 200+ 200+Impact F/R (in-lb) 160/160 160/160Color, Tristimulus -0.07 -0.06Gloss, 60.degree. 92.7 91.4Gloss, 20.degree. 77.1 73.4RESISTANCE PROPERTIESHumidity (60.degree. C.), 432 504Time (hrs)Appearance Increased No(after testing) Microblisters ChangeSalt Spray,Time (hrs) 1070 1070Creepage (mm) 1 1Appearance No Change No Change(after testing)______________________________________
EXAMPLE 6
Curable compositions I was prepared by the method described in EXAMPLE 2. It was cured at 175.degree. and 190.degree. C. by the method described in EXAMPLE 2.
______________________________________ Weight (g)______________________________________COMPOSITION IRucote .RTM. 101 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)Sulfonimide cure catalyst of EXAMPLE 1, 0.50PART ABenzoin (a solid additive) 2.40R960-48 titanium dioxide pigment 40.00Resiflow III flow control agent 1.30______________________________________
TABLE 5 summarizes the film properties and appearance characteristics of the cured coatings obtained by curing composition H.
This example illustrates that a sulfonimide cure catalyst of Example 1, Part A produces excellent powder coatings with Rucote.RTM. 101 as well as Alftalat.RTM. AN 745 and Arakote.RTM. 3109 polyesters at two different temperatures.
TABLE 5______________________________________Powder Coatings with Rucote .RTM. 101 and Powderlink .RTM. 1174Cured with a Sulfonimide Cure Catalyst CURABLE COMPOSITION I 175.degree. C. Cure 190.degree. C. Cure______________________________________FILM APPEARANCE Orange Peel Orange Peel Microblisters MicroblistersFILM PROPERTIESFilm Thickness 2.0-2.6 1.7-2.4(mils)Film Thickness 0.051-0.066 0.043-0.061(mm)Hardness KHN.sub.25 11.9 10.8MEK Rubs 200+ 200+Impact F/R (in-lb) 160/160 160/160Color, Tristimulus -0.06 -0.07Gloss, 60.degree. 83.5 91.7Gloss, 20.degree. 66.7 74.6RESISTANCE PROPERTIESHumidity (60.degree. C.), 336 504Time (hrs)Appearance Some loss No(after testing) of gloss ChangeSalt Spray,Time (hrs) 1070 1070Creepage (mm) 1 3Appearance Some blisters Some blisters(after testing)______________________________________
EXAMPLE 7
An additional sulfonimide cure catalyst was prepared by the method of EXAMPLE 1, PART A, using the same reaction conditions but different reactants:
di-(4-Chlorobenzene)sulfonimide, prepared from 4-chlorobenzenesulfonamide and 4-chlorobenzenesulfonyl chloride.
Two additional curable compositions were prepared as follows:
______________________________________ Weight (g)______________________________________COMPOSITION JArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)di-(Benzene)sulfonimide cure catalyst 0.30Benzoin (a solid additive) 1.40R960-48 titanium dioxide pigment 40.00Resiflow P67 flow control agent 1.30COMPOSITION KArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)di-(4-Chlorobenzene)sulfonimide 0.30cure catalystBenzoin (a solid additive) 1.40R960-48 titanium dioxide pigment 40.00Resiflow P-67 flow control agent 1.25______________________________________
Compositions J and K, along with Composition E from EXAMPLE 4 were cured at 190.degree. C./20 min by the method of EXAMPLE 2. The results are summarized in TABLE 6.
This example illustrates that both symmetrical and unsymmetrical sulfonimide cure catalyst of the invention are effective catalysts. It further illustrates that N-(methanesulfonyl)-p-toluenesulfonamide sulfonimide cure catalyst produces excellent film properties and acceptable appearance.
TABLE 6______________________________________Effect of Symmetrical and UnsymmetricalCure Catalyst on Film Properties and Appearance CURABLE COMPOSITIONS Comp. Comp. Comp. E J K______________________________________FILM APPEARANCE Orange Orange Orange Peel Peel Peel Micro- Micro- Micro- blisters blisters blisters Some Wrinkles WrinklesFILM PROPERTIESFilm Thickness 2.4-2.9 2.0-3.0 1.8-2.2(mils)Film Thickness 0.061-0.074 0.051-0.076 0.046-0.056(mm)Hardness, KHN.sub.25 12.1 12.4 11.8MEK Rubs 20/200+ 200+ 200+Impact F/R (in-lb) 160/160 160/160 110-120/40-50Color, Tristimulus -0.06 -0.04 0.05Gloss, 60.degree. 92.7 93.9 95.1Gloss, 20.degree. 78.6 75.0 81.8RESISTANCEPROPERTIESHumidity (60.degree. C.), 456 600 600Time (hrs)Appearance Loss of No change No changeafter testing glossSalt Spray, 1008 1008 1008Time (hrs)Creepage (mm) 1 0 0Appearance 9 9 9after testing______________________________________
EXAMPLE 8
This example illustrates that a large variety of non-sulfonimide compounds are unsuitable as catalysts in the composition of this invention, when compared to Composition E of Example 4 under the same conditions. The results are summarized in Table 7.
It is concluded from the results in Table 7 that Composition E containing the sulfonimide of Example 1, Part A, has better overall properties when compared with related catalyst systems.
TABLE 7__________________________________________________________________________COMPARISON OF FILM PROPERTIES OF SULFONIMIDES WITH OTHER CATALYSTSIN POWDER COATINGS GLOSS APPEARANCE MEK RUBS IMPACT, F/R 60.degree./20.degree. BEFORE TESTING__________________________________________________________________________Composition E Containing 20/200+ 160/160 92.7/78.6 Orange Peelthe Sulfonimide of MicroblistersEXAMPLE 1, PART A ##STR22## 1/3 -- -- -- ##STR23## 1/5 -- -- -- ##STR24## <1 -- -- --NH.sub.2 SO.sub.3 H 1/12 -- -- -- ##STR25## 200+ 160/120-140 71.8/23 Wrinkles Craters ##STR26## 200+ 60-80/0-20 (Fail) 79.4/32.8 Orange Peel Microblisters Pinholes ##STR27## 50/200 50-60/0-5 29.4/6.4 Textured__________________________________________________________________________
EXAMPLE 9
This example illustrates that powder coating compositions of the invention containing sulfonimide cure catalyst of the invention cure faster and produce films with superior overall film properties and appearance characteristics than similar compositions containing benzoin tosylate as the cure catalyst.
The following curable compositions, Curable Composition L and Curable Composition M, were formulated and thereafter cured at 175.degree. C. (20 min) and at 190.degree. C. (20 min.) the procedure of EXAMPLE 2.
______________________________________ Weight (g)______________________________________COMPOSITION LArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.00Agent (solid)Sulfonimide Cure Catalyst of 0.5EXAMPLE 1, PART ABenzoin (a solid additive) 2.4R960-48 titanium dioxide pigment 40.00Resiflow P-67 flow control agent 1.3COMPOSITION MArakote .RTM. 3109 polyester (solid) 94.00Powderlink .RTM. 1174 Crosslinking 6.0Agent (solid)Benzoin tosylate (solid) 2.0Benzoin (a solid additive) 1.4R960-48 titanium dioxide pigment 40.00Resiflow P-67 flow control agent 1.25______________________________________
Table 8 summarizes the film properties and appearance characteristics of the cured films obtained by curing the comparative pair (Compositions L and M) at 175.degree. C. Table 9 depicts the same at 190.degree. C.
It is concluded from the results in Tables 8 and 9 that films obtained by curing the compositions of the invention have superior film properties and appearance characteristics than similar films cured with benzoin tosylate. It can also be concluded that higher levels of benzene tosylate catalyst are needed to achieve cure compared to sulfonimide catalysts.
TABLE 8______________________________________Comparison of a Sulfonimide Cure Catalystof the Invention withBenzoin Tosylate in Powder Coatings Cured at 175.degree. C. Sulfonimide* Benzoin Tosylate Curable Comp. L Curable Comp. M______________________________________FILM APPEARANCE Orange Peel Orange Peel Microblisters MicroblistersFILM PROPERTIESFilm Thickness 1.5-2.2 2.0-2.2(mils)Film Thickness 0.038-0.056 0.051-0.059(mm)Hardness, KHN.sub.25 11.3 11.9MEK Rubs 20/200+ 1/15Impact F/R (in-lb) 160/160 20-30/0-5Color, Tristimulus -0.06 -0.06Gloss, 60.degree. 81.1 92.4Gloss, 80.degree. 56.5 79.5RESISTANCE PROPERTIESHumidity (60.degree. C.), 504 96Time (hrs)Appearance No change Loss of Glossafter testingSalt Spray, 888 528Time (hrs)Creepage (mm) 3 0Appearance Blisters Blistersafter testing______________________________________ *N-Methanesulfonyl-p-Toluenesulfonamide, sulfonimide catalyst of EXAMPLE 1, PART A
TABLE 9______________________________________Comparison of a Sulfonimide Cure Catalystof the Invention withBenzoin Tosylate in Powder Coatings Cured at 190.degree. C. Sulfonimide* Benzoin Tosylate Curable Curable Composition L Composition M______________________________________FILM APPEARANCE Orange Peel Orange Peel Microblisters MicroblistersFILM PROPERTIESFilm Thickness 1.5-2.2 1.6-2.0(mils)Film Thickness 0.038-0.056 0.041-0.056(mm)Hardness, KHN.sub.25 11.2 11.6MEK Rubs 200+ 200+Impact F/R (in-lb) 160/160 150-160/150-160Color, Tristimulus -0.05 -0.06Gloss, 60.degree. 93.5 94.4Gloss, 80.degree. 74.9 83.4RESISTANCE PROPERTIESHumidity (60.degree. C.), 504 264Time (hrs)Appearance No change Increasedafter testing MicroblistersSalt Spray, 960 528Time (hrs)Creepage (mm) 4 0Appearance Blisters Blistersafter testing______________________________________ *N-Methanesulfonyl-p-Toluenesulfonamide, sulfonimide catalyst of EXAMPLE 1, PART A
EXAMPLE 10
This example illustrates that solvent-based coating compositions of the invention containing a sulfonimide cure catalyst cure at a rate comparable with sulfonic acid-cured compositions.
______________________________________ Weight (g)______________________________________COMPOSITION NJONCRYL .RTM. 500 Acrylic 81.25Resin (80% Solids)CYMEL .RTM. 1168 Crosslinking Aqent 35.00di-Benzenesulfonimide (52% Solution) 1.00n-Butanol 20.00Xylene 16.55Non-Volatiles: 65 Weight %Resin/Crosslinker: 65/35Weight RatioCatalyst based on: 0.5 Weight %resin solidsCOMPOSITION OJONCRYL .RTM. 500 Acrylic 81.25Resin (80% Solids)CYMEL .RTM. 1168 Crosslinking Agent 35.00p-Toluenesulfonic Acid (40 Wt % Solution) 0.75n-Butanol 20.00Xylene 16.55Non-Volatiles: 65 Weight %Resin/Crosslinker: 65/35Weight RatioCatalyst based on: 0.3 Weight %resin solids______________________________________
Curing of Compositions N and O
The curable compositions N and O were applied on Bonderite 100 Cold Roll Steel (CRS) substrate panels by means of a #46 wire cator applicator and were cured by heating at a cure schedule of 30 minutes at 121.degree. C. (250.degree. F.). The cured film was evaluated by standard methods widely accepted by the coatings industry. The physical properties of the cured films obtained by curing composition N and Composition O are listed in Table 10. Table 10 shows that the composition cure rates are comparable. This is unexpected since the acidity of sulfonimide catalysts is lower than p-toluenesulfonic acid for comparable cures. The potlife is also improved and the appearance of the cured film is better.
It is concluded from this example that sulfonimide cure catalysts of this invention are effective catalysts in solvent-based coatings, and that they cure at a rate comparable to the widely used sulfonic acid catalysts.
TABLE 10______________________________________Cure Response of Solvent-Based CoatingsComparison of Sulfonimide and Sulfonic Acid Catalysts COMPOSITION N.sup.(a) COMPOSITION O.sup.(b)______________________________________Film ThicknessMils 1.65-1.75 1.65-1.75mm 0.042-0.044 0.042-0.044121.degree. C./30 min CureHardness, KHN.sub.25 8.0 9.0MEK Rubs 200+.sup.(c) 200+135.degree. C./30 min CureHardness, KHN.sub.25 9.7 9.6MEK Rubs 200+ 200+149.degree. C./30 min CureHardness, KHN.sub.25 10.1 10.0MEK Rubs 200+ 200+______________________________________ .sup.(a) Composition containing dibenzenesulfonimide. .sup.(b) Composition containing p-toluenesulfonic acid. .sup.(c) Film scratches off with difficulty using fingernail immediately after 200 double rubs (film scratched while wet with MEK).
EXAMPLE 11
This example illustrates lower yellowing of sulfonimide-cured compositions relative to sulfonic acid cured compositions in base coat/clear coat solvent-based coatings under overbake cure conditions.
WHITE BASE COAT
The base coat was prepared by a procedure similar to the procedure described in Example 10 using the following ingredients and conditions:
______________________________________ Weight (g)______________________________________Base Coat Formulation AJONCRYL .RTM. 500 Acrylic 60.00Resin Solids (80% Solids)OR-650 Titanium Dioxide Pigment 80.00Methyl Amyl Ketone 18.00BYK .RTM. P 104-8 Wetting Agent 0.80(a product of Byk-Mallinckrodt Company,Wallingford, CT)Base Coat Formulation BJONCRYL .RTM. 500 Acrylic 40.00Resin Solids (80% Solids)CYMEL .RTM. 303 Crosslinking Agent 20.00n-Butanol 15.00p-Toluenesulfonic Acid (40% Solution) 1.00______________________________________
After grinding Formulation A in a 3-roll mill, Formulation B was added to ground Formulation A, and applied to ED-3150A primed EP1-P60 panel, available from Advanced Coating Technologies, Hillsdale, Mo., using a #34 wire cator applicator. The resulting panels were cured at 121.degree. C. (250.degree. F.) for 15 minutes, and thereafter the clear topcoat Composition P and Composition Q (infra) were each applied to two separate panels coated with the base coat.
______________________________________CLEAR TOP COAT COMPOSITIONS Weight (g)______________________________________COMPOSITION PJONCRYL .RTM. 500 Acrylic 81.30Resin (80% Solids)CYMEL .RTM.1170 Crosslinking Agent 35.00di-Benzenesulfonimide 0.52n-Butanol 16.00Xylene 21.50Non-Volatiles: 65 Wt. %Resin/Crosslinker Weight Ratio: 65/35Catalyst based on Resin Solids: 0.5 Wt. %COMPOSITION QJONCRYL .RTM. 500 Acrylic 81.30Resin (80% Solids)CYMEL .RTM. 1170 Crosslinking Agent 35.00p-Toluenesulfonic Acid 0.30n-Butanol 16.00Xylene 21.50Non-Volatiles: 65 Wt. %Resin/Crosslinker Weight Ratio: 65/35Catalyst based on Resin Solids: 0.3 Wt. %______________________________________
The clear coat Compositions P and Q were each applied onto base-coated panels using a #46 wire cator applicator and thereafter cured; first at 121.degree. C./30 minute cure followed by an additional 149.degree. C./30 minute cure, simulating overbake condition which commonly occur in a coating process. The results are summaried in Table 11.
It is concluded from the results in Table 11 that the solvent-based coatings compositions of the invention containing the novel sulfonimide cure catalysts of the invention have better overbake tolerance than sulfonic acid catalyzed compositions when cured under overbake conditions.
TABLE 11______________________________________Yellowing of Solvent-Based Base-Coat/Clear-CoatCoatings Under Overbake ConditionsComparison of Sulfonimide and Sulfonic Acid Catalysts COMPOSITION P.sup.(a) COMPOSITION Q.sup.(b)______________________________________Film Thicknessmils/mmBase Coat 1.26/0.032 1.28/0.032Clear Coat 1.59/0.040 1.48/0.038Hardness, KHN.sub.25(Clear Coat)121.degree. C./30 min cure 0.8 8.0121.degree. C./30 min cure + 9.3 10.3149.degree. C./30 min overbakeYellow Index121.degree. C./30 min cure -1.56 -1.28121.degree. C./30 min cure + +2.18 +5.32149.degree. C./30 min overbakeTotal Color change 2.71 4.39(difference of E)______________________________________ .sup.(a) Composition containing dibenzenesulfonimide. .sup.(b) Composition containing ptoluenesulfonic acid.
EXAMPLE 12
This example illustrates an embodiment in which a 1:1 blend of sulfonimide cure catalyst and polyfunctional material is used to obtain Composition R, which is a curable composition containing catalyst/polyfunctional material combination of the invention.
PREPARATION OF CATALYST/POLYFUNCTIONAL MATERIAL COMBINATION
A mixture of dibenzenesulfonimide (10.0 g) and Alftalat.RTM. AN745 solid polyester (10.0 g) was melt-mixed at 150.degree. C. The resinous material thus obtained was cooled to room temperature and the resulting solids crushed to give a catalyst/polyfunctional material combination usable in the method of the invention.
______________________________________COMPOSITION R Weight (g)______________________________________Arakote .RTM. 3109 polyester (solid) 93.50Powderlink .RTM. 1174 crosslinking agent (solid) 6.00Catalyst/polyfunctional material combination 1.00of this example as prepared abovecontaining 1:1 weight ratio of dibenzene-sulfonimide and Alftalat .RTM. AN745 polyesterBenzoin (a solid additive) 1.40R960-48 Titanium dioxide pigment 40.00Resiflow P67 flow control agent 1.30______________________________________
Composition R was cured at 190.degree. C./20 min by the method of EXAMPLE 2. The results are summarized in TABLE 12. As seen from Table 12, good film appearance (no wrinkles), film properties such as cure, impact, and gloss, and resistance properties such as resistance to humidity and salt spray are obtained. This embodiment, therefore, is within the scope of the invention.
TABLE 12______________________________________Powder Coatings Prepared byUsing a Catalyst Polyfunctional Material Combination.sup.ain a Curable Composition (Composition R)______________________________________FILM APPEARANCE Orange Peel, Microblisters, Microcraters in some areas, No WrinklesFILM PROPERTIESFilm Thickness (mils) 1.3-2.4(mm) 0.033-0.061Hardness, KHN.sub.25 11.2MEK Rubs 200+Impact F/R (in-lb) 160/160Color, Tristimulus -0.08Gloss, 60.degree. 95.320.degree. 83.3RESISTANCE PROPERTIESHumidity (60.degree. C.), Time (hrs) 504Appearance After Testing No ChangeSalt Spray, Time (hrs) 1008Creepage (mm) 0Appearance After Testing No Change______________________________________ .sup.a. Dibenzenesulfonimide/Alftalat .RTM. AN745 Polyester (1:1 weight ratio) combination at 1 wt % level based on total resin solids, corresponding to 0.5 wt % level of dibenzenesulfonimide based on total resin solids in Composition R.
EXAMPLE 13
The experiment of Example 12 was repeated with the following modifications:
1. Masterbatching was carried out using phenyl-p-tolylsulfonimide instead of dibenzenesulfonimide.
2. COMPOSITION S was prepared by using the masterbatch described in Example 13, part 1 (above) instead of the dibenzenesulfonimide masterbatch in Composition R of Example 12.
3. COMPOSITION T was prepared by replacing the Arakote.RTM. 3109 polyester in Composition S with Alftalat.RTM. AN745 polyester.
4. COMPOSITION U was prepared by replacing the Arakote.RTM. 3109 polyester in Composition S with Rucote.RTM. 101 polyester.
Table 13 summarizes the results obtained by curing the compositions S, T, and U by the 190.degree. C./20 min protocol described in Example 12. The embodiments represented by Compositions S, T, and U, having good film properties, are also within the scope of the invention.
__________________________________________________________________________EXAMPLE 13Powder Coatings Prepared by Using Phenyl-p-tolylsuflonimide/Alftalat AN 745 Polyester Combination COMPOSITION COMPOSITION COMPOSITION S T U__________________________________________________________________________FILM APPEARANCE Orange Peel Orange Peel Orange Peel Microblisters Microblisters Microblisters Microcraters on edgesFILM PROPERTIESFilm Thickness(mils) 1.5-3.1 1.7-2.4 1.6-2.4(mm) 0.038-0.079 0.043-0.061 0.041-0.061Hardness, KHN.sub.25 11.8 11.3 11.1MEK Rubs 200+ 200+ 200+Impact F/R (in-lb) 160/160 160/160 160/160Color, Tristimulus -0.09 -0.09 -0.09Gloss, 60.degree. 93.2 94.0 91.120.degree. 72.3 72.3 75.4RESISTANCE PROPERTIESHumidity (60.degree. C.), Time (hrs) 504 504 504Appearance After Testing No Change No Change No ChangeSalt Spray, Time (hrs) 1056 1056 528Creepage (mm) 0 0 0Appearance After Testing No Change few blisters blisters__________________________________________________________________________
Although the present invention has been described with reference to certain preferred embodiments, it is apparent that modifications and changes thereof may be made by those skilled in the art, without departing from the scope of this invention as defined by the appended claims.

Claims

1. A composition of matter comprising:
(i) a solid sulfonimide cure catalyst, and
(iii) a solid polyfunctional material capable of reacting with an aminoplast crosslinking agent,
wherein the solid sulfonimide cure catalyst is selected from the group consisting of:
(a) a sulfonimide represented by the formula
RSO.sub.2 NZSO.sub.2 R
wherein each of the R groups is, independently, selected from the group consisting of
(a1) a linear, branched or cyclic alkyl, fluoroalkyl or N,N-dialkylamino group of 1 to 20 carbon atoms, or mixtures thereof,
(a2) an aryl group of 1 to 20 carbon atoms containing 5 or less aromatic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups are the same or different groups selected from the group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkyl aminocarbonyl and N,N-dialkyl aminocarbonyl groups, and
(a3) an aralkyl group wherein the alkyl and the aryl groups have the same meaning as the alkyl and aryl groups (a1) and (a2), and
wherein the Z group is
(a4) hydrogen,
(a5) acyl or
(a6) an alkyl or aralkyl group of 1 to 20 carbon atoms;
(b) a sulfonimide represented by the formula
--(R'--SO.sub.2 NH--SO.sub.2)--.sub.n
wherein n groups of the --(R'--SO.sub.2 NH--SO.sub.2)--units may be the same or different, and the R' group in each of the n units is independently selected from the group consisting of
(b1) a linear, branched or cyclic alkylene or fluoroalkylene group of 1 to 20 carbon atoms,
(b2) an arylene group of 1 to 20 carbon atoms containing 5 or less carbocyclic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups are the same or different groups selected from the group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkyl aminocarbonyl and N,N-dialkyl aminocarbonyl groups, and
(b3) an aralkylene group wherein the alkylene and the arylene groups have the same meaning as the alkylene and arylene groups (b1) and (b2);
(c) a sulfonimide represented by the formula
P--(SO.sub.2 NHSO.sub.2 R").sub.n
wherein P is a polyfunctional group or a polymer of a number average molecular weight greater than 500, R" is an alkyl or aryl group of 1 to 20 carbon atoms, and n is 2 or greater; and
(d) a latent reactive form thereof.
2. The composition of claim 1 wherein the solid sulfonimide catalyst (i) is represented by the formula
RSO.sub.2 NZSO.sub.2 R
wherein each of the R groups is, independently, selected from the group consisting of:
(a1) a linear, branched, or cyclic alkyl, fluoroalkyl, or N,N-dialkylamino group of 1 to 20 carbon atoms, or mixtures thereof;
(a2) an aryl group of 1 to 20 carbon atoms containing 5 or less aromatic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups are the same or different groups selected from the group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxyl, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkylaminocarbonyl and N,N-dialkyl aminocarbonyl groups; and
(a3) an aralkyl group wherein the alkyl and the aryl groups have the same meaning as the alkyl and aryl groups as in (a1) and (a2) above; and
wherein the Z group is selected from a group consisting of:
(a4) hydrogen;
(a5) acyl; and
(a6) an alkyl group or an aralkyl group of 1 to 20 carbon atoms.
3. The composition of claim 1 wherein the reactive group of the polyfunctional aminoplast reactive material (iii) is selected from the group consisting of carboxy, hydroxy, carbamate, amino, amido, mercapto and mixtures thereof.
4. The composition of claim 3 wherein the solid polyfunctional material (iii) is a polyfunctional hydroxy reactant material selected from the group consisting of epoxy or polyurethane prepolymers, alkyds, acrylic resins containing pendant or terminal carboxy or hydroxy functionalities, or polyester resins with pendant or terminal hydroxy or carboxy functionalities.
5. The composition of claim 2 wherein the solid polyfunctional material (iii) is a polyfunctional hydroxy reactant material selected from the group consisting of epoxy or polyurethane prepolymers, alkyds, acrylic resins containing pendant or terminal carboxy or hydroxy functionalities, or polyester resins with pendant or terminal hydroxy or carboxy functionalities.
6. The composition of claim 5 wherein the sulfonimide cure catalyst is represented by the formula: ##STR28## wherein X is independently selected from the group consisting of hydrogen, chloro, methyl, alkyl, nitro, amino, cyano, alkoxycarbonyl, carboxyl, acyl, N-alkylamino, carbonyl, and N,N-dialkylaminocarbonyl groups.
7. The composition of claim 6 wherein the sulfonimide cure catalyst is represented by the formula: ##STR29##
8. The composition of claim 6 wherein the sulfonimide cure catalyst is represented by the formula: ##STR30##
9. The composition of claim 6 wherein the sulfonimide cure catalyst is represented by the formula: ##STR31##
10. The composition of claim 5 wherein the sulfonimide cure catalyst is represented by the formula: ##STR32##
11. The composition of claim 5 wherein the weight ratio of the sulfonimide cure catalyst (i) to the polyfunctional material (iii) is about 3:1 to about 1:20.
12. The composition of claim 5 wherein the polyfunctional material (iii) has a number average molecular weight between from about 100 to about 50,000.
13. The composition of claim 5 wherein the polyfunctional material (iii) is selected from a carboxy functional polyester resin and a carboxy functional acrylic resin.
14. The composition of claim 5 wherein the polyfunctional material (iii) is selected from a hydroxy functional polyester resin and a hydroxy functional acrylic resin.
15. A process for the preparation of a solid cure catalyst/polyfunctional material combination comprising the steps of:
(1) heating a mixture of (i) a solid sulfonimide cure catalyst and (iii) a solid polyfunctional material capable of reacting with an aminoplast crosslinking agent, at a temperature sufficient to produce a uniform melt-mixed resinous material;
(2) cooling said melt-mixed resinous material to a temperature sufficient to produce a solid; and
(3) crushing the solid to produce a powdered sulfonimide cure catalyst/polyfunctional material combination,
wherein the solid sulfonimide cure catalyst is selected from the group consisting of:
(a) a sulfonimide represented by the formula
RSO.sub.2 NZSO.sub.2 R
wherein each of the R groups is, independently, selected from the group consisting of
(a1) a linear, branched or cyclic alkyl, fluoroalkyl or N,N-dialkylamino group of 1 to 20 carbon atoms, or mixtures thereof,
(a2) an aryl group of 1 to 20 carbon atoms containing 5 or less aromatic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups are the same or different groups selected from the group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkyl aminocarbonyl and N,N-dialkyl aminocarbonyl groups, and
(a3) an aralkyl group wherein the alkyl and the aryl groups have the same meaning as the alkyl and aryl groups (a1) and (a2), and
wherein the Z group is
(a4) hydrogen,
(a5) acyl or
(a6) an alkyl or aralkyl group of 1 to 20 carbon atoms;
(b) a sulfonimide represented by the formula
--(R'--SO.sub.2 NH--SO.sub.2)--.sub.n
wherein n groups of the --(R'--SO.sub.2 NH--SO.sub.2)-- units may be the same or different, and the R' group in each of the n units is independently selected from the group consisting of
(b1) a linear, branched or cyclic alkylene or fluoroalkylene group of 1 to 20 carbon atoms,
(b2) an arylene group of 1 to 20 carbon atoms containing 5 or less carbocyclic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 groups are the same or different groups selected from the group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxy, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkyl aminocarbonyl and N,N-dialkyl aminocarbonyl groups, and
(b3) an aralkylene group wherein the alkylene and the arylene groups have the same meaning as the alkylene and arylene groups (b1) and (b2);
(c) a sulfonimide represented by the formula
P--(SO.sub.2 NHSO.sub.2 R").sub.n
wherein P is a polyfunctional group or a polymer of a number average molecular weight greater than 500, R" is an alkyl or aryl group of 1 to 20 carbon atoms, and n is 2 or greater; and
(d) a latent reactive form thereof.
16. The process of claim 15 wherein the solid sulfonimide catalyst (i) is represented by the formula
RSO.sub.2 NZSO.sub.2 R
wherein each of the R groups is, independently, selected from the group consisting of:
(a1) a linear, branched, or cyclic alkyl, fluoroalkyl, or N,N-dialkylamino group of 1 to 20 carbon atoms, or mixtures thereof;
(a2) an aryl group of 1 to 20 carbon atoms containing 5 or less aromatic or heterocyclic aromatic rings substituted by R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 groups are the same or different groups selected from the group consisting of hydrogen, fluoro, alkyl, fluoroalkyl, aryl, haloaryl, carboxyl, mercapto, vinyl, chloro, bromo, cyano, nitro, sulfonyl, acyl, alkoxycarbonyl, alkoxy, perfluoroalkoxy, hydroxy, amino, acylamino, alkoxycarbonylamino, carbamoyl, aminocarbonyl, N-alkylaminocarbonyl and N,N-dialkyl aminocarbonyl groups; and
(a3) an aralkyl group wherein the alkyl and the aryl groups have the same meaning as the alkyl and aryl groups as in (a1) and (a2) above; and
wherein the Z group is selected from a group consisting of:
(a4) hydrogen;
(a5) acyl; and
(a6) an alkyl group or an aralkyl group of 1 to 20 carbon atoms.
17. The process of claim 15 wherein the solid polyfunctional material (iii) is a polyfunctional hydroxy reactant material selected from the group consisting of epoxy or polyurethane prepolymers, alkyds, acrylic resins containing pendant or terminal carboxy or hydroxy functionalities, or polyester resins with pendant or terminal hydroxy or carboxy functionalities.
18. The process of claim 15 wherein the weight ratio of the sulfonimide cure catalyst (i) to the polyfunctional material (iii) is about 3:1 to about 1:20.
19. The composition of claim 1 wherein the weight ratio of the sulfonimide cure catalyst (i) to the polyfunctional material is from about 1:10,000 to about 9:1.
20. The composition of claim 19 wherein the weight ratio of the sulfonimide cure catalyst (i) to the polyfunctional material (iii) is from about 1:10,000 to about 9:1.
21. The composition of claim 2 wherein the solid sulfonimide cure catalyst is represented by the formula: ##STR33## wherein X is independently selected from the group consisting of hydrogen, chloro, methyl, nitro, amino, cyano, alkoxycarbonyl, carboxyl, acyl, N-alkylaminocarbonyl, and N,N-dialkylaminocarbonyl groups.
22. The composition of claim 21 wherein the solid sulfonimide cure catalyst is represented by the formula: ##STR34##
23. The composition of claim 21 wherein the solid sulfonimide cure catalyst is represented by the formula: ##STR35##
24. The composition of claim 21 wherein the solid sulfonimide cure catalyst is represented by the formula: ##STR36##
25. The composition of claim 3 wherein the polyfunctional material (iii) has a number average molecular weight between from about 100 to about 50,000.
26. The composition of claim 4 wherein the polyfunctional material is selected from a carboxy terminated polyester and a carboxy functional acrylic resin.
27. The composition of claim 4 wherein the polyfunctional material is a hydroxy functional acrylic resin or a hydroxy functional polyester resins.
28. The process of claim 15 wherein the temperature of the melt is from about 50.degree. to 200.degree. C.
29. The process of claim 15 wherein the cooling temperature of the melt-mixed material is in the range from about -20.degree. C. to about 50.degree. C.

Parent Case Info

This application is a divisional of application Ser. No. 07/976,916, filed Nov. 16, 1992, which is a divisional of application Ser. No. 07/688,022, filed Apr. 19, 1991, now U.S. Pat. No. 5,256,493, which is a continuation-in-part of application Ser. No. 07/512,041, filed Apr. 26, 1990, now abandoned.

US Referenced Citations (21)

Number	Name	Date
3927141	Feldman et al.	Dec 1975
4031036	Koshar	Jun 1977
4064191	Parekh	Dec 1977
4071526	Dotzer et al.	Jan 1978
4089827	Massy et al.	May 1978
4118437	Parekh	Oct 1978
4133813	Isaksen	Jan 1979
4166169	Patel et al.	Aug 1979
4271277	Golownia	Jun 1981
4281075	Chattha	Jul 1981
4387222	Koshar	Jun 1983
4510290	Kirchmayr et al.	Apr 1985
4525535	Craun et al.	Jun 1985
4540735	Borovicka, Sr.	Sep 1985
4542180	Carlson et al.	Sep 1985
4608410	Borovicka, Sr.	Aug 1986
4649168	Kress et al.	Mar 1987
4788076	Weiss	Nov 1988
4873295	Kurosawa et al.	Oct 1989
4877838	Toman	Oct 1989
4920175	Kanda et al.	Apr 1990

Foreign Referenced Citations (5)

Number	Date	Country
0084515 A2	Jul 1983	EPX
0139609 A1	May 1985	EPX
0144810 A2	Jun 1985	EPX
9132	Feb 1955	DEX
2854440 A1	Jul 1979	DEX

Non-Patent Literature Citations (5)

Entry
Chatta & Bauer "Latent Acid Catalysts for Hydroxy/Melamine Catalysts", Ind. Eng. Chem. Prod. Res. Dev., 1983, vol. 44, pp. 440-444.
Bentz & Nischk, "Synthesis of Disulfonimides, N-Sulfonyl Carboxamides, and Alpha Oxo N-Sulfonyl Carboxamides", Angew Chem. Internat. Edit., 1970, vol. 9(1), pp. 66-67.
EPO Search Report dated Dec. 2, 1992, for Application No. 91118437-2.
EPO Search Report dated Jul. 3, 1991 for Application No. 91102858-7.
Derwent Abstract No. 91-318918, Oct. 27, 1991.

Divisions (2)

	Number	Date	Country
Parent	976916	Nov 1992
Parent	688022	Apr 1991

Continuation in Parts (1)

	Number	Date	Country
Parent	512041	Apr 1990

Sulfonimide catalysts polyfunctional material combination

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Abstract