CA1238742A - Aqueous coating compositions and methods for preparing same - Google Patents

Abstract

F-2079(2080) AQUEOUS COATING COMPOSITIONS AND
METHODS FOR PREPARING SAME

ABSTRACT

Aqueous compositions suitable for sanitary can coatings comprise the neutralized water dispersible ionic polymer product of the reaction of an epoxy resin with an acid polymer, and a different resin which is not necessarily self-dispersible in water. The different resin is introduced either preformed at any stage or is prepared, in situ, in the presence of the epoxy resin esterified with acid polymer either before or after the ionic epoxy resin-acid polymer product is dispersed in water. The epoxy resin-acid polymer product acts as a polymeric surfactant capable of keeping even the normally non self-dispersible second polymer in stable dispersion in water.

Description

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F-2079(2080) -1-AQUEOUS COATING COMPOSITIONS AND
METHOOS FOR PREPARING SAME

This invention relates to aqueous coating compositions and methods for preparing same.
A variety of aqueous coating compositions comprising epoxy resins and acrylic polymers are known in the art and several are commercially available. In order to obtain desirable characteristics for many critical end use applications, such as coatings for sanitary cans, it is considered necessary to include a high proportion of epoxy resin in the composition. Epoxy contents of 60 to 80 percent are commonly used. Typical epoxy acrylate compositions are disclosed in U.S. Patent Nos. 4,247,439, 4,212,781, 4,308,185 and 4,~02,373.
U.S. Patent No. 4,285,847 discloses epoxy acrylic compositions in which the epoxy acrylic is made by free-radical grafting of ionizable side chains onto an epoxy backbone; dispersing this product ln water and thereafter polymerizing, in situ, addition polymerizable monomers which may or may not also contain ionizable groups. Ry this means the solids conten~ of the composition is increased and the proportion of total epoxy resin in the composition is reduced by replacement with the cheaper addition polymer thereby reducing the cost of the composition.
In accordance with the present invention cost reduction as well as several other advantages over U.S. Patent 4,285,847 are obtained. By using an epoxy acrylate prepared by an esterification reaction between an epoxy resin and an acrylic polymer instead of the graft epoxy-acrylic of U.S. Patent 4,285,847, benefits are obtained in the latitude of solids and viscosity which can be conveniently obtained, and in the ability to reduce the amount of ~' ~Y ~- .

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F-2079(2080) -2-am~ne neutralizing agent necessary to obtain stable water dispersions having useful viscosity.
The present invention resides in one aspect in an aqueous coating composition comprising A. an ionic polymer component containing sufficient carboxyl groups to render it self dispersible in water in neutralized form which is the reaction product of an epoxy resin containing 1,2~ep~y groups, and a preforn~d addition poly~r~ containing carboxyl groups, said ionic polymer containing hydroxy ester groups from the reaction of 1,2-epoxy groups on said epoxy resin with carboxyl groups on said preformed addition polymer, and ~eing substantially free o~ unreacted 1,2-epoxy groups;

B. an addition polymer different from said preformed addition polymer defined in (A); and C. ammonia or an organic amine neutralizing agent in an amount sufficient to render the composition stably dispersible in water.

In a further aspect, the invention resides in a method for preparing a coating composition comprising the steps o~

~ A. preparing an ionic polymer component containing sufficient carboxyl groups to render it self dispersible in water in neutralized form by reacting an epoxy rcsin containing 1,2-epoxy groups, and a preformed addition polymer containing carboxyl groups, said ionic polymer containing hydroxy ester groups ~rom the reaction of 1,2-epoxy groups on said epoxy resin with carboxyl groups on said preformed addition polymer9 and being substantially free of unreacted 1,2-epoxy groups;

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F-2079(2080) -3-B~ dispersing said ionic polymer component in water with the addition of ammonia or an organic amine neutralizing agent in an amount suf~icient to render the composition stably dispersible in water; and C. incorporating an addition polymer difFerent from said addition polymer defined in (A) into the aqueous dispersion of said ionic polymer component.

Conveniently, said incorporating step is effected by mixing the different addition polymer with the pre~ormed addition polymer prior to reaction with the epoxy resin or by mixing the different addition polymer with the ionic polymer component before, during or after dispersal thereof in ~ater. Alternatively, the diffe~ent addition polymer can be prepared in situ in the presence of the ionic polymer dispersion in which case the ionic polymer acts as a polymeric sur~actant.

The ionic polymer component A o~ said coating composition :is prepared by reackion of a preformed addition polymer containing carboxyl groups with an epoxy resin containing 1,2 epoxy groups, conveniently using the methods disclosed in U.S~ Patent 4,247,439 or U.S. Patent 4,302,373. It may, however, be necessary to modify conditions to promote esterification instead of quaternization, for example by using tertiary amine in an amount which is less than su~icient to react with all of the epoxy groups on the epoxy resin.
Briefly, the reaction between the epoxy resin and the preformed addition polymer containing carboxyl groups is conducted in the presence of a tertiary amine, with the conditions being chosen so that an esteri~ication reaction occurs between the epoxy :,' .
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F-2079(2080) -4-groups of the epoxy resin and the carboxyl groups o~ the addition polymer. By way of contrast, the reaction conditions in the a~orementioned patents are selected in order to promote a reaction between the tertiary amine and epoxy groups giving quaternary ammonium groups in accordance with a well known reaction. It is believed that the reaction which is intended to promote esterification also results in the formation of significant amounts of quaternary ammonium groups by reaction between the epoxy groups and the tertiary amine. Indeed, more of the epoxy groups may be converted to quaternary ammonium groups than are converted to hydroxy ester linkages. Also, the reaction described in said patents intended to produce quaternary ammonium groups can, under appropriate condi-tions, result in significant ester formation. The products prepared in accordance with the present process there~ore can contain significant, even predominant amounts of quaternary groups, providing that hydroxy ester groups obtained by the reaction of epoxy groups with carboxyl groups are also present. A-t a minimum at least 5 percent of the epoxy groups on the epoxy resin should be converted to hydroxy ester groups. Whatever the relative proportions o~ quaternary and hydroxy ester groups, the polymer component A is ionic in character and is substantially free of unreacted 1,2-epoxy groups.
The ionic polymer may contain carboxyl polymer grafted to carbon atoms on the epoxy resin backbone but it is preferred that the polymer is prepared under conditions where grafting is avoided.
In general, the epoxy resin constitutes at least about 40 percent of the ionic polymer and the carboxyl containing polymer comprises the balance. Preferably the epoxy content is at least 60 percent and most preferably about 75 percent.
A w de variety of epoxy resins may be used herein but the preferred epoxy resins are aromatic polyethers, particularly those derived ~rom the oondensation o~ a bisphenol such as Bisphenol A, '. , . : ~ -' . -' ' ~ 2~
F-2079(2080) -S-and epichlorohydrin. These epoxy resins possess hydroxy groups inaddition to epoxy groups. The higher the molecular weight of the epoxy resin the more hydroxy groups are present. These hydroxy groups can participate in the final curing reaction. The preferred epoxy resins are aromatic polyethers having a number average molecular weight (Mn) of at least 1,500. However, the n~m~er average molecular weight of these resins can vary from 350 to 6000.
As recognized in the art, epoxy resins prepared by the condensation o~ bisphenols and epichlorohydrin contain a mixture of diepoxides, monoepoxides and aromatic polyethers which are ~ree of epoxy groups. The average functionality of such mixtures may range widely from 0.2 epoxy groups per molecule to nearly 2 epoxy groups per molecule. Suitable mixtures of epoxy resins can be obtained by reacting a lower molecular weight epoxy resin having a ~unctionality of between 1 and 2, for example, with a defunctionalizing agent which is capable of reacting with the epoxy groups. The de~unctionalizing agent can contain carboxyl groups, hydroxy groups or amide groups. Specific suitaDle materials include acids such as benzoic acid and fatty acids such as octanoic acid; hydroxy compounds such as phenols, in particular bisphenols and lower alkanols; and amides such as acrylamide. Defunctionalization with bisphenols is of` particular interest since the epoxy resin is thereby upgraded to higher molecular weight at the same time as some of the epoxy groups are defunctionalized.
The carboxyl polymer is prepared by the addition polymerization o~ ethylenically unsaturated monomers comprising at least about 20 percent of an ethylenically unsaturated carboxylic acid based on the total weight of the monomers. Polymers and copolymers of this type are well known although the copolymers with particularly high proportions of carboxylic acid as preferred herein are somewhat unusual. Preferably the carboxyl containing polymer is ~' ~
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F-2079(2080) -6-a copolymer with ethylenically unsaturated monomers which are non-reactive under the contemplated conditions of polymerization and reaction with epoxy resin. However, small amounts of reactive . .
monomers, e.g., hydroxy monomers such as 2-hydroxy ethylmethacrylate9 amide monomers such as acrylamide, and N-methylol monomers such as N-methylol acryLamide, can be used. Suitable non-reactive monomers are, ~or example, acrylate and mzthacrylate esters such as ethyl acrylate, methyl acrylate, butyl acrylate, styrene or vinyl toluene, vinyl acetate, vinyl chloride, vLnylidene chloride, and acrylonitrile. The function of these monomers is to enhance solvent solubility and to provide good film formation.
Otherwise the nature and proportions are not critical.
The presence of a large proportion of carboxyl functional monomer is important. The preferred minimum proportion of carboxyl monomer is 30 percent of the weight of the monomers used to prepare the carboxyl containing polymer. Methacrylic acid provides the best hydrolytic stability and is very much preferred, but other acids such as fumaric acid, acryLic acid, crotonic acid and itaconic acid are useful. Up to about 80 pqrcent of the monomers can be carboxyl functional, the maximum being determined by retention of solvent solubility of the copolymer.
The preferred polymers containing carboxyl groups generally having a number average molecular weight (Mn) in the range of ~000 to 20,000, preferably 3,000 to 6,400. Molecular weight can be controlled by monomer content during polymerization9 catalyst concentration and polymeri ation temperature in known manner.
Mercaptan chain termination is preferably avoided especially where the product is intended for use in coating of sanitary cans because of the offensive odor o~ mercaptans.
Generally, the addition polymer containing carboxyl groups is preformed and is reacted with the epoxy resin as a solvent , . . .. .
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7~ r F-2079(2080) ~7-soLution in the presence of sufficient amine, preferably a tertiary amine,to promote the reaction. However, the addition copolymer can also be prepared by reacting a carboxyl containing monomer such as methacr~lic acid with the epoxy group in the presence of tertiary amine and subsequently polymerizing additional monomers, in situ.
The reaction between the oxirane groups of the epoxy resin and the carboxyl groups o~ the addition polymer is carried out in the presence of an esterification catalyst.
The preferred esterification catalysts are tertiary amines, particularly dimethylaminoethanol,but other esterification catalysts,particularly tertiary amines such as dimethylbenzylamine, trimethylamine, and tributylamine,can be used. The amount of catalyst used can vary widely. For example, where a tertiary amine is used as little as 0.1-û.3 percent by weight of the catalyst based on the total amount of epoxy resin and carboxyl containing polymer can be used nr the amount can be much larger up to about 10 percent and more of the reactants.
Another way of defining the amount of amine used is the relation to the total carboxyl content of the acid polymer. The amount of amine present during the reaction o~ the epoxy resin and carboxyl polymer should be sufficient to neutralize from about 5 to 50 percent of the carboxyl groups in the acid polymer. Preferably, the amine is suf~icient to neutralize between 10 and 35 percent of the carboxyl groups. Still another way of defining the amount of tertiary amine present during reaction of the epoxy resin and carboxyl polymer is by the equivalent ratio of amine to 1,2-epoxy groups. Preferably, this ratio is less than one thereby ensuring that some of the epoxy groups will be consumed in hydroxy ester formation by reaction with carboxyl groups.
The amount of amine has a significant effect on the nature of the product of the reaction. In general9 the smaller the amount 7~;~
F-2079(2080) -8-of amine present during reaction the higher the viscosity of the product. This difference in viscosity is apparent in both the solvent solution and when the product is emulsified in water. The e~fect of the a~ount of amine used is observed even where the total amount of amine present in the dispersed product is identical.
Thus, for example, the same product is not obtained when amine is present at the 40 percent neutralization level during reaction as when amine sufficient to neutralize 5 percent of the car~oxyl groups is present during reaction and supplemented with 35 percent of the neutralization amount prior ta dispersion in water.
The amount of amine present during reaction also has a pronounced effect on the particle size of the final dispersion. The relationship of amirle content to particle size is illustrated in the following examples.
The second polymer different from the addition polymer used to prepare the ionic epoxy resin-acid polymer product can be prepared from a wide variety of unsaturated monomers. Particularly preferred are monomers which are free oF functional groups reactive with epoxy resin or which would render the polymer self-dispersible in water. For example there may be mentioned the esters of acrylic and methacrylic acid such as methyl acrylate, butyl acrylate, methyl methacrylate and butyl methacrylate; aromatic monomers such as styrene and methylstyrene; vinyl and vinylidene halides such as vinyl chloride and vinylidene chloride; isoprene; butadiene; and acrylonitrile. In certain applications it may be advantageous to include in the copolymer self-crosslinking monomers such as N-methylol acrylamide or N-isobutoxy acrylamide. Presently preferred monomers include styrene, methylstyrene and butyl acrylate and acrylonitrile.
The second polymer can be introduced at any convenient stage of the reaction. Preferably, the second polymer is prepared9 .

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in situ, in the presence of an aqueous dispersion of the ionic epoxy-acidic polymer reaction product. The reaction is conducted in known manner and advantageously is initlated by a redox system.
Inorganic or organic peroxides such as hydrogen peroxide or t-butyl hydroperoxide; or persulfates such as ammonium persulfate and alkali metal persulfates can be coupled with a suitable reducing agent such as hydrazine, ammonium or alkali metal sulfites, bisul~ites, metabisul~ites or hydrosul~ites. The procedures disclosed in U.S.
Patent 4,285,847 are suitable for conducting the polymerization.
The second polymer can also be introduced as a pre~ormed polymer into either the aqueous dispersion of the ionic epoxy-acid polymer product or can be mixed with the ionic epoxy resin-acid polymer product before it is dispersed in water. Similarly, the second polymer can be mixed with a solvent solution of the acidic polymer prior to its reaction with the epoxy resin either by making the addition polymers separately or by preparing one in the presence of the other. The proportion of the second polymer in the composition can vary widely. The maximum is limited by the amount which can be stably dispersed in water by the ionic polymer component and the retention of desired film properties. Usually the weight ratio of the second addition polymer (B) to the ionic polymer (A) ls from 0.05:1 to 10:1 but more preferably is 0.2;1 to 5:1.
The resins used in preparing the compositions o~ this invention are used by dissolution in a volatile organic solvent. A
wide variety o~ solvents are suitable. Organic solvents~of limited water miscibility, such as xylene, toluene, butanol and

2-butoxyethanol are useful, and they may be used alone or together with water miscible sblvents, such as 2-ethoxyethanol or methyl ethyl ketone.
The final composition includes su~ficient ammonia or amine to render the mixture self-dispersible in water. Preferably, a .
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F-2079(2080) -10-tertiary amine such as dimethylethanolamine is used. In general, the total amount of an amine or an ammonia present in the Final product will be sufficient to neutralize at least 25 to 90 percent of the carboxyl groups present in the polymers used to prepare their composition. Finally, compositions, as used, preferably include a curing agent such as an aminoplast or a phenoplast resin in an amount of 1 to 25 percent, preferably from 3 to 10 percent, based on the solids of the composition.
In some cases it may be found that the process described above yields an aqueous coating composition containing an undesirable residue of the monomer used to produce the second polymer. For example, the use of styrene and butyl acrylate in the preparation of the second polymer may result in a product having an objectionable odor due to residual butyl acrylate which polymerizes more slowly than styrene. In such a case, the undesired monomer residue can be reduced by conducting an additional polymerization step in the presence of the second polymer containing residual monomer, with another monomer which is capable of copolymerizing with the undesired mollomer and which results in a less undesirable monomer residue or a residue which is more easily removable. For example, where the monomer residue is butyl acrylate an additional polymerization step using further styrene as the comonomer can be effected on the second polymer at any convenient stage during preparation of the coating composition.
This invention is illustrated by the following non-limiting examples.

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~-207~(2080) A polymer surfactant dispersion is prepared by reacting an acid containing acrylic prepolymer with an epoxy resin, neutralizing wlth base and dispersing in water.
The acrylic prepolymer is prepared as follows:

Parts by Weight Butanol 2755.2 Methacrylic Acid 1197.7 Styrene 597.8 EthyL Acrylate 197.5 Benzoyl Peroxide 142.8 (70~, Water Wet) 2-Butoxyethanol 1995.8 6886.8 The butanol is charged to a 12-liter reactor equipped with a stirrer, reflux condenser, thermometer, addition funnel and nitrogen inlet. A premix is made of the monomers and benzoyl peroxide and 20 percent is added to the reactor. The nitrogen flow is started and the reactor is heated to 93~C and held at this temperature for 15 minutes. The remaining premix is added uni~ormly over 5 hours while maintaining 93C. After the premix is added, the temperature is held for two hours to complete the polymerization.
The 2-butoxyethanol is then added to dilute the prepolymer. The resulting solution has a solids content of 30.3 percent, an acid number of 385 and a viscosity of 2600 centipoise.
An epoxy acrylate adduct is formed by esterifying an epoxy resin with the above acrylic prepolymer under amine catalysis as follows:

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~31~7~2 F-2079(2080) -12-Parts by Weight DER 3311 698.1 - 3isphenol A 374.9 2-Butoxyethanol 116.8 Tri-n-butylamine 2.2 Acrylic Prepolymer 1299.0 Dimethylaminoethanol (first portion) 28.6 Dimethylaminoethanol (second portion) 40.4 "Cymel 11562'* 107.7 Deionized Water 2331.5 4999.2 lDER-331 (Dow Chemical Co.) - A 182-190 epoxy equivalent ~eight diglycidyl ether of bisphenol A ~D~R-331 is a tradem~r~.
2Cymel 1156"(American Cyanamid Co.) - A butylated melamine curing agent.
The first four items above are charged to a 5-liter reactor with stirrer, reflux condenser, thermometer and nitrogen inlet.
Nitrogen flow is started and the reactants are heated to 130C.
After exotherm, 150C is maintained until the oxirane content of the reaction mixture falls to 0.37 meq/g. The acrylic prepolymer is then added. The mixture is stirred until uniform and the temperature is adjusted to 94C. The first portion of dimethylaminoethanol (esteri~ication catalyst) is then added and this temperature is held for 3 hours. The reaction mixture turns from opaque to translucent and the acid number drops by the amount indicating complete reaction of the epoxy. The epoxy acrylate resin solution has a solids content of 57.3, an acid number o~ 85.0 and a specific viscosity of 0.33. There is no residual oxirane content.
To form a dispersion, the epoxy acrylate adduct is furthe~
neutralized with the second portion of ~imethylaminoethanol and the curing agent is added. Water is added with efficient stirring to produce a stable9 small particle size dispersion with a solids content of 31.5 percent.

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f-207Y(2080) EXAMPLE 2 ~

The above polymeric surfactant dispersion (2,000 parts) is transferred to a 5 liter reactor together with 500 parts of deionized water and 30 parts of dimethylaminoethanol. A nitrogen blanket is applied and the reactor is heated to 80C. A mixture of 303 parts of styrene and 17 parts of benzoyl peroxide (70Y0, water wet) is added with stirring over ~ hrs. at 80C. Then, t-Butyl hydroperoxide (0.5 part) is added. After a 5-minute wait, O.S parts of sodium bisulfite in 15 parts water is added over 15 minutes. The emulsion is held at 80C for 1/2 hour. Water (800 parts) is added and the emwlsion is cooled. The product has a solids content of 24.1 percent acid number of 62, speoific viscosity of 0.76 and dispersion viscosity o~ 125 cp.
The above emulsion was drawn down on aluminum and tinplate substrates and baked for 2 minutes at 400~F. Properties of gloss, adhesion, wedgebend flexibility and pasteurization resistance were all rated excellent at beer and soft drink weights.

The polymeric surfactant of Example 1 (2000 parts) is charged to a 5 liter reactor together with 500 parts of deionized water and 5 parts of sodium bisulfite. The mixture is heated to 65C under a nitrogen blanket. A premix of 225 parts of styrene9 75 parts of acrylonitrile and 5 parts of t-butyl hydroperoxide (70%) is added over 1 hour at 65 and the mixture then held for an additional 1/2 hour. An additional 0.5 parts of t-butyl hydroperoxide (70~) is added. After 5 minutes a mixture of 0.5 parts sodium bisulfite in 15 parts water is added. Temperature (65C) is held for an additional 1/2 hour, then a mixture of 800 parts water and 15 parts , - '' ', . ~: ~

, ~lZ3 F-2079(2080) -14-diméthylaminoethanol are added. The resulting coating emulsion has a solids content of 24.8 percent, an acid number of 59.5 and viscosity of 85 centipoise.
Test results on aluminum and tinplate panels, as in Example 2, all produced excellent results.

An epoxy acrylate polymeric surfactant dispersion is formed by reacting an epoxy resin with the acrylic prepolymer of Example I
under tertiary amine esterification catalysis as follows:

Parts bv Weight ~Epon 828"1 ttrademark) 1445,0 Bisphenol A 780.2 2-Butoxyethanol 245.0 Tri-n-butylamine 4.6 Acrylic prepolymer of Example f 2674.0 Deionized Water I38.9 Dimethylaminoethanol 89.0 Dimethylaminoethanol 79.1 Cymel 1156" (trademark) ' 150.2 Deionized Water ' 4944.2 ~M 1~550.2 l." Epon 8281l(Shell Chemical Co.) - An 182-l90 epoxy equivalent weight diglycidyl ether of bisphenol A.
The procedure of the epoxy acrylate preparation and dispersion of Example I are followed with the exception that a minor amount of water is added with the acrylic prepolymer to help control reaction viscosity and temperature. The resulting polymer has an acid number of 85.7. The dispersion product has a solids content of 29.2~, a pH of ~.8, viscosity of 12,600 centipoise and particle size 0.17 microns.
The above polymeric sur~actant dispersion (4500 parts) is charged to a 12 l reactor together with 4320 parts of deionized - . : . .
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, F-2079(208Q) -15-water, 27 parts of dimethylaminoethanol and 21 parts of ammonium bisulflte ~45%). The mixture is heated to 65~ under a nitrogen blanket. A premix of 657 parts of styrene, 657 parts of butyl acrylate and 8.73 parts of t-butyl hydroperoxide (90/0) is added over 2 hours at 65C and the mixture then held for an additional 1/2 hour. An additional 0.9~ parts of t-butyl hydroperoxide (70~) is added. After 5 minutes a mixture of 1.8 parts ammonium bisulfite and 27 parts of water is added. Temperature (65~C) is held for an additional 1/2 hr. The resulting emulsion product has a solids content of 25.5%, a pH of 7.1, an acid number of 51.0 and viscosity (Brookfield) of 1140 centipoiseO
Test results on aluminum and tin plate panels, as in Example 2, all produced excellent results.

The emulsion product of Example 4 (4000 parts) is mixed with 222 parts of butanol, 882 parts of water and 9.43 parts of dimethylaminoethanol until uniform. The resulting finish, which is réady for spray liner application, has a solids content of lg.gYo~ a pH of 7.4, surface tension of 26.2 dynes/cm and viscosity of ~6 sec as measured by ~4 Ford Cup.
Test results on spray application using aluminum and tinplate cans produced blister-~ree interior can coatings with excellent enamel rater coverage. The sprayed coatings also showed excellent adhesion, reverse impact resistance and pasteurization reslstance.

A series of compositions were prepared in the manner described in Example 4. The amount of dimethylaminoethanol present during reaction of the epoxy resin and the carboxyl containing .
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F-2079(2080) -16-acrylic copolymer was varied in increments from 10 percent to 35 percent of the amount necessary to neutralize the carboxyl groups of the acrylic copolymer. Results of reduced specific viscosity, viscosity and particle size were measured at various stages of the process. The results are summarized in Tables I and II. It is evident that the amount of amine present during the reaction between epoxy resin and the carboxyl group containing acrylic copolymer has a profound effect on the viscosity and particle size of the ionic polymer and that this effect is also evident after the styrene-butyl acrylate polymer is introduced.

TABLE I

IONIC RESIN SOLUTION IONIC RESIN_DISPERSION
% Cat* Part. Size EX. _ DMEOA Y NV AN RSV** ~ NV _ _pH Visc. Y Neut Microns 6 i0 57.5- 90.8 0-.39~ 29-.2 6.833,750 38.3 0.23 7 12 57.8 ~0.1 0.36 29.2 6.820.750 37.1 0.21 8 14 58.7 88.8 0.33 29.3 6.810,46û 37.3 0.18 g 16 58.3 89.0 0.32 29.2 6.69,340 38.4 0.17 18 56.8 89.4 0.31 29.3 6.85,800 38.3 0.17 11 20 57.3 8~.4 0.29 29.0 6.83,200 38.5 0.16 ~2 25 58.5 90.4 0.26 29.8 6.7590 37.1 0.24 13 30 57.3 88.4 0.25 29.4 6.7366 40.3 0.27 14 35 58.6 87.0 0.25 29.5 6.8280 41.1 0.39 *Percent neutralization of acrylic prepolymer.
**Reduced speoific viscosity - 1~ by weight of dry resin in dimethylformamide at 25C.

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F~2079(2080) -17-TABLE II
DISPERSION OF IONIC RESIN
AND COPOLYMER
IONIC RESIN DISPERSION (24.8 + .2% solids) % Cat.*
EXAMPLE DMEOA RSV** Visc. Part. Size RSV*** Visc. Part Size (cp) Microns (cp) _ Microns .
6 10 0.39 33,75~ 0.230.81 1410 0.25 7 12 0.36 20,750 0.210.63 630 0.30 8 14 0.33 10,460 0.180.70 500 ~.28 g 16 0.32 9,340 0.170.65 275 0.27 18 0.31 5,800 0.170.68 200 0.27 11 20 0.29 3,200 0.160.80 110 0.27 12 25 0.26 590 0.240.7g 31 0.31 13 30 0.25 366 0.270.60 2i 0.39 14 35 0.25 280 0.390.61 16 0.57 *Percent neutralization of acrylic polymer.
**Reduced specific viscosity - 1~ by weight of dry resin in dimethylformamide at 25C.
*~*Reduced Speci~ic viscosity - 1% by weight o~ dry resin in tetrahydrofuran at 25C.

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F-2079(2080) -18-A. ~
~~- A 12 1 reactor equipped with stirrer, reflux condenser, thermometer, heating mantle and nitrogen blanket was charged with 3800.7 parts butanol. A premix of 1652.4 parts glacial methacrylic acid, 824.4 oarts styrene, 275.4 parts ethyl acrylate and 197.1 parts benzoyl peroxide (70~ water wet) was also prepared. Twenty percent of the premix was added to the reactor wnich was heated to 93C under nitrogen and held at temperature for 15 minutes. The remaining premix was added over 5 hours at 93C after which this temperature was held ~or 2 hours. Butanol (225000 parts) was added to give an acrylic prepolymer solution at 33.5~ NV, acid number of ~92 and viscosity of 9660 centipoise.
In a five liter reactor equipped as ab*ove were charged 65.5 parts of 2-butoxyethanol, 655.9 parts ~oon 828, 364.5 parts bispnenol A and 2.1 parts tri-n-butylamine. The charge was heated to 136C and allowed to exotherm to 175C, then held at 150C for 1.5 hours. The upgraded epoxy was defunctionalized 33~ b~ addition of 27.0 parts stearic acid to an epoxy value of 0.21 meq~g oxirane.
2-Butoxyethanol 164.0 parts, 100 parts butanol and 551.2 parts o~
the above acrylic containing 29.6 parts of a 25% aqueous solution of trimethylamine esterification catalyst were added. A cloudy~ opaque mixture was formed which was held at reflux (1~9C) for oonstant acid number. At the end of 2.5 hours, the mixture had cleared completely and reached the acid number, 46.7, calculated for complete oxirane esterification. 2-Hexoxyethanol 18.û parts, dimethylaminoethanol, 54.4 parts and"Cymel 1156, 61.5 parts were added and stirred unkil unif~rm. Deionized water (2242 parts) was added to form a dispersion. After transfer to a 6 1 container, 33 parts butanol and 17 parts 2-butoxyethanol were added and a ~inish was prepared at 19.5% NV by addition of deionized water.
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F-2079t2080) -19-B. Preparation of St~rene/Butyl Acr~late Modified_Epoxy-Acrylate Twenty three hundred parts of the above dispersion was transferred to a 5 1 reactor equipped as before. A premix of 76.9 parts styrene, 76.9 parts butyl acrylate and 0.02 parts t-butyl hydroperoxide (90~) was prepared and emulsified in the reactor under a nitrogen blanket where it was heated to 65C. A premix of 1.5 parts of ammonium bisulfite in 15 parts water was added and 70C was held for 3.0 hours. To remove any butyl acrylate residue, a premix of 3804 parts styrene and 0.13 parts of t-butylhydroperoxide (9C~) was then added followed in five minutes by a premix of 3.5 parts ammonium bisulfite in 5 parts water. The styrene overpolymerization was complete after holding at 70C for 2 hours. A spray finish at 20% NV was prepared by the addition of deionized water. The finish gave excellent properties for the coating of can interiors including resistance to fracturing on a 40F can drop test which is not passed by epoxy acrylates modified with 30% styrene add-on. The dispersion had a pleasant odor not objectionable for use as a commercial can coating.

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Claims (10)

F-2079(2080) -20-CLAIMS:

1. An aqueous coating composition comprising A. an ionic polymer component containing sufficient carboxyl groups to render it self dispersible in water in neutralized form which is the reaction product of an epoxy resin containing 1,2-epoxy groups, and a preformed addition polymer containing carboxyl groups, said ionic polymer containing hydroxy ester groups from the reaction of 1,2-epoxy groups on said epoxy resin with carboxyl groups on said preformed addition polymer, and being substantially free of unreacted 1,2-epoxy groups;

B. an addition polymer different from said preformed addition polymer defined in (A); and C. ammonia or an organic amine neutralizing agent in an amount sufficient to render the composition stably dispersible in water.

2. The composition of claim 1 in which the neutralizing agent is dimethylaminoethanol.

3. The composition of claim 1 in which said addition polymer containing carboxyl groups is a polymer of methacrylic acid.

4. The composition of any of claims 1, 2 or 3 in which said 1,2-epoxy resin is an epichlorohydrin-bisphenol A epoxy resin.

F-2079(2080) -21-

5. The composition of any of claims 1, 2 or 3 in which said addition polymer (B) is a copolymer of styrene and butyl acrylate.

6. The composition of any of claim 1, 2 or 3 in which said ionic polymer component (A) is the reaction product of epichlorohydrin-bisphenol A epoxy resin, an addition copolymer of methacrylic acid, ethyl acrylate and styrene, and dimethylaminoethanol; said addition polymer (B) is the copolymer of styrene and butyl acrylate; and the neutralizing agent (C) is dimethylaminoethanol in an additional amount than used to prepare (A).

7. A method for preparing a coating composition comprising the steps of A. preparing an ionic polymer component containing sufficient carboxyl groups to render it self dispersible in water in neutralized form by reacting an epoxy resin containing 1,2-epoxy groups, and a preformed addition polymer containing carboxyl groups, said ionic polymer containing hydroxy ester groups from the reaction of 1,2-epoxy groups on said epoxy resin with carboxyl groups on said preformed addition polymer, and being substantially free of unreacted 1,2-epoxy groups;

B. dispersing said ionic polymer component in water with the addition of ammonia or an organic amine neutralizing agent in an amount sufficient to render the composition stably dispersible in water; and C. incorporating an addition polymer different from said addition polymer defined in (A) into the aqueous dispersion of said ionic polymer component.

F-2079(2080) -22-

8. The method of claim 7 in which the different addition polymer of step (C) is formed, in situ, by polymerization in the presence of the aqueous dispersion of said ionic polymer component.

9. The method of claim 7 or claim 8 in which said ionic polymer component is prepared in the presence of a tertiary amine in an amount sufficient to react with 10 to 35 percent of the carboxyl groups on said addition polymer containing carboxyl groups.

10. A method as claimed in claim 7 or claim 8 in which said different addition polymer is formed by addition-polymerization of a first monomer such that a residue of the first monomer remains and the method includes the further step of reducing the amount of the residue of said first monomer by conducting a further polymerization step in the presence of said different addition polymer containing residual first monomer, with a second monomer which is capable of copolymerizing with said first monomer and which results in a less undesirable monomer residue or a residue which is more easily removable than said first monomer.