USRE31310E - Impact resistant vinyl ester resin and process for making same - Google Patents

Impact resistant vinyl ester resin and process for making same Download PDF

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Publication number
USRE31310E
USRE31310E US06/124,055 US12405580A USRE31310E US RE31310 E USRE31310 E US RE31310E US 12405580 A US12405580 A US 12405580A US RE31310 E USRE31310 E US RE31310E
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acid
polydiene
rubber
thermosettable resin
resin
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Daniel J. Najvar
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Dow Chemical Co
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00—Chemical modification by after-treatment
    • C08F8/08—Epoxidation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4292—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/02—Condensation polymers of aldehydes or ketones with phenols only of ketones

Definitions

  • thermosettable vinyl ester resin by the reaction of an unsaturated monocarboxylic acid such as methacrylic acid with a polyepoxide is known. While the physical properties of the cured resin can be varied depending on the choice of reactants, the choice of monomer copolymerizable with the resin and the like, the properties may also be modified by adding various materials to the resin. Inert reinforcing materials such as glass fibers and inert fillers such as CaCO 3 or kaolin clay are commonly employed both to improve properties and to reduce costs.
  • additives are also known: thickening agents, thermoplastic low profile (smooth surface) additives, rubbery polymers to improve impact resistance, and the like.
  • compatibility of these additives with the resin may frequently be a major problem which calls for other additives to stabilize the system.
  • Some of the additives are also susceptible to removal from the cured resin by contact with solvents and the like. Consequently, the advantages of certain additives may be lost or diminished in value because of these problems.
  • thermosettable resin that inherently provides all of the desired properties. This ideal may never be reached but an object of this invention is to inherently provide improved impact resistance in the vinyl ester resin by chemically incorporating a polydiene rubber into the thermosettable resin itself. Other objects, benefits and advantages of the invention will become readily apparent from the description which follows.
  • the objects and benefits of this invention are obtained by a modified process for making vinyl ester resins wherein a polyepoxide is reacted with an unsaturated monocarboxylic acid and a liquid carboxy terminated polydiene rubber.
  • the combined acid equivalents of said unsaturated acid and polydiene rubber ranges from about 0.8 to 1.2 equivalents per epoxide equivalent. At least about 80 percent of the acid equivalents comprises the unsaturated acid and the balance between 0.01 and 20 percent comprises the polydiene rubber, provided that the polydiene rubber content of the resin is at least about 4 weight percent.
  • novel vinyl ester resins are useful as powder coatings as well as in admixture with copolymerizable monomers to prepare reinforced plastic articles.
  • Terminally unsaturated vinyl ester resins possess a number of outstanding properties which account for their commercial acceptance in such areas as molding resins, corrosion resistant reinforced plastic pipe and other vessels, glass fiber laminates, and the like. But like most thermosettable resins, vinyl ester resins do not possess outstanding impact resistance.
  • Vinyl ester resins are generally prepared by reacting together about equivalent amounts of an unsaturated monocarboxylic acid and a polyepoxide.
  • any of the known polyepoxides may be employed in the preparation of the vinyl ester resins of this invention.
  • Useful polyepoxides are glycidyl polyethers of both polyhydric alcohols and polyhydric phenols, flame retardant epoxy resins based on tetrabromo bisphenol A, epoxy novolacs, epoxidized fatty acids or drying oil acids, epoxidized diolefins, epoxidized diunsaturated acid esters as well as epoxidized unsaturated polyesters, so long as they contain more than one oxirane group per molecule.
  • the polyepoxides may be monomeric or polymeric.
  • Preferred polyepoxides are glycidyl polyethers of polyhydric alcohols or polyhydric phenols having equivalent weights per epoxide group of about 150 to 1500, preferably about 250 to 700 and more preferred about 400 to 600. Generally, as the epoxide equivalent weight decreases the amount of carboxy terminated rubber increases.
  • the polyepoxides are characterized by the presence of more than one epoxide group per molecule.
  • Unsaturated monocarboxylic acids include acrylic acid, methacrylic acid, halogenated acrylic or methacrylic acids, cinnamic acid and the like and mixtures thereof, and hydroxyalkyl acrylate or methacrylate half esters of dicarboxylic acids as described in U.S. Pat. No. 3,367,992 wherein the hydroxyalkyl group preferably has from two to six carbon atoms.
  • Said acid is generally reacted with the polyepoxide in the proportions of about 1 equivalent of acid per each equivalent of epoxide, but the proportions of equivalents may range from about 0.8/1 to 1.2/1, respectively.
  • liquid it is meant to include the low molecular weight polydienes of about 2000 to 20,000 molecular weight and preferably about 3,000 to 10,000.
  • acid equivalents employed in the process at least about 80 percent comprises said unsaturated acid and the balance between about 0.01 and 20 percent comprises said polydiene, provided that the polydiene rubber content of the resin is at least about 4 weight percent.
  • carboxy terminated is meant that the polydiene rubber is terminated at each end with an acid carboxy, --COOH, group.
  • the particular liquid carboxy terminated polydienes used in this invention may be prepared by any suitable means.
  • One procedure involves solution polymerization of a conjugated diene monomer in the presence of an organo metal catalyst.
  • the lithium catalysts and in particular the dilithium catalysts such as dilithiobutane, dilithium stilbene, dilithium napthalene and the like are preferred.
  • dilithium catalysts the polymer obtained is terminated at each end by a lithium atom.
  • Treatment of said polymer with carbon dioxide replaces the lithium atoms with carboxy lithium salt groups.
  • the polymer is treated with acid to convert the lithium salt to the free acid form.
  • Carboxy terminated polymers of various conjugated dienes or mixtures of same may be prepared in this manner.
  • the conjugated dienes may have from 4 to 12 carbon atoms and preferably from 4 to 8.
  • Typical monomers include 1,3-butadiene, isoprene, piperylene, methylpentadiene, 3,4-dimethyl-1,3 hexadiene and the like.
  • carboxy terminated liquid copolymers of a conjugated diene and a copolymerizable vinyl monomer include alkenyl aromatics such as styrene, vinyl toluene, ⁇ -methyl styrene etc.; nitriles such as acrylonitrile, methacrylonitrile, etc.; acrylate and methacrylate esters such as the methyl, ethyl, propyl, cyclohexyl etc. esters; heterocyclic nitrogen-containing monomers such as the various vinyl pyridine isomers, etc.; vinyl chloride, vinylidene chloride, methyl vinyl ether and the like. Said copolymers should contain at least 40 weight percent of diene and correspondingly from 0 to about 60 weight percent of at least one copolymerizable vinyl monomer different from said diene monomer.
  • Preferred copolymer polydienes are the liquid carboxy terminated acrylonitrile/butadiene copolymers and particularly preferred are those copolymers prepared from 12 to 25 percent acrylonitrile and 88 to 75 percent butadiene.
  • the vinyl ester resins typically are prepared in the presence of catalysts such as the organophosphonium salts, tertiary amines such as 2,4,6-tri(dimethylaminomethyl) phenol [DMP-30] and the like.
  • catalysts such as the organophosphonium salts, tertiary amines such as 2,4,6-tri(dimethylaminomethyl) phenol [DMP-30] and the like.
  • Various vinyl polymerization inhibitors such as hydroquinone or its methyl ether and the like may be present during the reaction or added after the resin forming reaction. If desired the reaction may be run in an inert solvent, preferably one which can be readily removed by evaporation etc. after the resin has been prepared.
  • the carboxy terminated polydiene may be reacted with the polyepoxide first followed by addition and reaction of the unsaturated monocarboxylic acid or both acid reactants may be added and reacted with the polyepoxide at the same time.
  • the polydiene rubber modified vinyl ester resin produced herein typically contains terminal polymerizable groups and associated therewith a hydroxyalkylene group, e.g. --CH 2 CH(OH)CH 2 --, formed by the reaction of the acid carboxy group with the epoxide group.
  • This hydroxyl group may be used for further modification, e.g. by a post-reaction with a dicarboxylic acid anhydride in proportions up to about 1 mole per equivalent of hydroxyl.
  • a modification of this kind is disclosed in U.S. Pat. No. 3,564,074.
  • Other materials which are reactive with hydroxyl groups e.g. isocyanates, acyl halides, etc. may be used to modify the vinyl ester resin.
  • Suitable dicarboxylic acid anhydrides containing ethylenic unsaturation include maleic anhydride, the halogenated maleic anhydrides, citraconic anhydride, itaconic anhydride and the like and mixtures thereof.
  • Saturated dicarboxylic acid anhydrides include phthalic anhydride, tetrabromophthalic anhydride, chlorendic anhydride, anhydrides of aliphatic unsaturated dicarboxylic acid and the like.
  • the rubber modified vinyl ester resins are higher molecular weight resins by virtue of chemically combining the carboxy terminated polydiene rubbers into the resin structure. Accordingly, many of the resins are suitable as powder coating materials. A mixture of the powdered resin with a peroxide or other catalyst may be readily cured at an elevated temperature. The pendant carboxyl groups are of importance in powder coatings since they can be reacted with metal oxides to make solid powdered even in the presence of liquid monomers.
  • the resins are more commonly used in admixture with a copolymerizable monomer to prepare laminates, glass reinforced plastic pipe, reinforced molded parts, and the like.
  • the rubber modified vinyl ester resin may be combined with up to 60 to 70 weight percent of monomer. The proportions will vary, somewhat depending on the monomer selected, other additives employed and other factors.
  • a variety of copolymerizable monomers are disclosed in the vinyl ester patents previously referred to.
  • Typical monomers are styrene, vinyl toluene, halogenated styrenes, alkyl substituted styrenes, alkyl substituted styrene, acrylic and methacrylic esters, hydroxyalkyl esters of acrylic and methacrylic acid, and the like. More usually the monomer content will range from about 30 to 60 weight percent.
  • the choice of monomer is also based on whether the resin is to be cured by thermal and/or chemical means or by high energy radiation.
  • chemical catalysts e.g. peroxides, persulfates, diazo compounds, etc.
  • heat styrene is a common monomer because of its low cost and availability as well as the properties obtained.
  • aromatic monomers such as butyl acrylate and hydroxyalkyl acrylates.
  • the rubber modified vinyl ester resin may be cured (thermoset) by various means.
  • Cure accelerators such as the metal organic acid salts, e.g. cobalt naphthenate, or tertiary amines such as N,N-dimethyl toluidine are frequently used with chemical catalysts.
  • Sensitizers or photoinitiators which reduce the radiation dosage may also be employed with radiation, especially with ultra violet light.
  • Other materials may be added to the resin such as inert reinforcing fibers, e.g.
  • the improved impact resistance of the rubber modified vinyl ester resins makes the resin especially useful in coatings and for molded articles.
  • molded parts such as motor housings for power mowers, boats and recreation products, automotive parts such as panels and housings, molded furniture containing blown saran microspheres where improved toughness and durability are required in medium density syntatic foams for chair legs and arms, doors, backup for acrylic faced bath tubs, lavatories, etc.
  • each of the uncured resins was non-blocking at 70° F. and could be powdered or flaked. Similar results are obtained if the copolymer is replaced by an equivalent amount of a carboxy terminated polybutadiene.
  • Tests were also made with some of the resins diluted to 50% styrene monomer. Clear castings were made by adding 1% benzoyl peroxide, curing at 100° C. for 1 hour and post-curing at 130° C. for 45 minutes.
  • resin E in which an unmodified vinyl ester resin (prepared by reacting equivalent amounts of an epoxy novolac, D.E.N. 438, with methacrylic acid) diluted to 25% styrene was blended therewith in varying amounts to vary the amount of rubber in the total resin. Clear castings were then made by curing with 1% benzoyl peroxide (BPO) at 80° C. for 6 hours and post curing for 30 minutes at 250° F. The casting at a 10% rubber level could be hammered and was slightly malleable whereas at 2.5% rubber the castings were brittle and shattered easily.
  • BPO benzoyl peroxide
  • a higher molecular weight polyepoxide was first prepared by reacting 6.5 lbs of bisphenol A with 6.58 lbs of D.E.R. 736 (an aliphatic diepoxide with an EEW of 175-205) in the presence of t-butyl phosphonium acetate catalyst. Then 4.05 lbs of a carboxy terminated butadieneacrylonitrile rubber similar to example 1, 6.97 lbs of methacrylic acid were added and reacted using a catalyst (DMP-30) and hydroquinone as an inhibitor. After the reaction was completed 36 lbs of styrene was added and mixed with the resin. The liquid resin had a viscosity of 57.7 cs.
  • a pipe collar was molded directly into a 12 inch pipe using the above formulation at 150° F.
  • the collar was demolded about 15 minutes after the formulation was accelerated with the DMA promoter.
  • the collar was aged for 24 hours and then tested for impact resistance. The collar passed a 20 foot drop test without breaking.
  • Another group of resins was prepared by heating together in the presence of a catalyst a polyepoxide or mixtures thereof, methacrylic or acrylic acid and a carboxy terminated butadiene/acrylonitrile rubber similar to that used in example 1. Heating was continued until the carboxy content reached a low value of less than 2%. Styrene monomer was then added. Clear castings were cured with 1% BPO and 0.2% DMA for one hour at 80° C. and post cured at 250° C. for 1 hour. The compositions of the resins and their physical properties are recorded in the following tables.
  • the polydiene rubber modified vinyl ester resins have improved adhesive properties as well as impact resistance.
  • Resins A, D and E of example 1 were used.
  • Resin A 0% rubber
  • All resins were diluted to 50% styrene.
  • An adhesive formulation with each resin was prepared by blending 20 parts per 100 parts of resin (phr) of MD-101 aluminum powder and 1 phr benzoylperoxide. Lap shear specimens were prepared according to ASTM-1002 using chromate etched aluminum strips, 1 ⁇ 4 ⁇ 0.064 inches. The adhesives were cured at 250° F. for 30 minutes and after cooling lap shear values were determined.
  • Carboxy rubber modified vinyl ester resins were compared to comparable resins without said rubber. McGarey cleavage tests were made by preparing test bars 6 ⁇ 1.2 ⁇ 0.25 inches in which a lengthwise cut was made on each side of the bar to one-third the thickness of the bar. At one end an initial 1 inch cut was made all the way through the bar to help initiate splitting. In each case the resin was cured with 1% benzoyl peroxide catalyst for 6 hours at 80° C. followed by 45 minutes at 250° F.
  • test bars were then split the length of the cut obtaining a stress-strain curve. Stress was applied at a rate of 0.05 inches per minute. The area under the plotted curve was taken to be representative of the work required to form the new split surface. At the same styrene level the test bar with no rubber content in the resin had an area under the stress-strain curve of 190 whereas the carboxy polydiene rubber containing resin had an area of 2350. The split in the latter case also showed a great deal of stress whitening along the crack propagation line which is an indication of toughness.

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Abstract

Vinyl ester resins with improved impact resistance and other benefits and advantages may be obtained by a process modification wherein up to 20 percent of the unsaturated monocarboxylic acid, which is reacted with a polyepoxide, is replaced by an equivalent amount of a liquid carboxy terminated polydiene rubber capable of reacting with epoxy groups to form a chemically bound molecule. .Iadd.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a continuation of my copending application Ser. No. 753,395 filed December 22, 1976, now abandoned, which, in turn, is a reissue of Ser. No. 343,716 filed March 21, 1973, U.S. Pat. No. 3,892,819. .Iaddend.
BACKGROUND .Iadd.OF THE INVENTION .Iaddend.
The preparation of a thermosettable vinyl ester resin by the reaction of an unsaturated monocarboxylic acid such as methacrylic acid with a polyepoxide is known. While the physical properties of the cured resin can be varied depending on the choice of reactants, the choice of monomer copolymerizable with the resin and the like, the properties may also be modified by adding various materials to the resin. Inert reinforcing materials such as glass fibers and inert fillers such as CaCO3 or kaolin clay are commonly employed both to improve properties and to reduce costs.
A variety of other additives are also known: thickening agents, thermoplastic low profile (smooth surface) additives, rubbery polymers to improve impact resistance, and the like. However, compatibility of these additives with the resin may frequently be a major problem which calls for other additives to stabilize the system. Some of the additives, unfortunately, are also susceptible to removal from the cured resin by contact with solvents and the like. Consequently, the advantages of certain additives may be lost or diminished in value because of these problems.
It would be desirable to have a thermosettable resin that inherently provides all of the desired properties. This ideal may never be reached but an object of this invention is to inherently provide improved impact resistance in the vinyl ester resin by chemically incorporating a polydiene rubber into the thermosettable resin itself. Other objects, benefits and advantages of the invention will become readily apparent from the description which follows.
SUMMARY
The objects and benefits of this invention are obtained by a modified process for making vinyl ester resins wherein a polyepoxide is reacted with an unsaturated monocarboxylic acid and a liquid carboxy terminated polydiene rubber. The combined acid equivalents of said unsaturated acid and polydiene rubber ranges from about 0.8 to 1.2 equivalents per epoxide equivalent. At least about 80 percent of the acid equivalents comprises the unsaturated acid and the balance between 0.01 and 20 percent comprises the polydiene rubber, provided that the polydiene rubber content of the resin is at least about 4 weight percent.
The novel vinyl ester resins are useful as powder coatings as well as in admixture with copolymerizable monomers to prepare reinforced plastic articles.
DESCRIPTION
Terminally unsaturated vinyl ester resins possess a number of outstanding properties which account for their commercial acceptance in such areas as molding resins, corrosion resistant reinforced plastic pipe and other vessels, glass fiber laminates, and the like. But like most thermosettable resins, vinyl ester resins do not possess outstanding impact resistance.
While impact resistance of vinyl ester resins can be improved by adding certain polydiene rubbers (see U.S. Pat. No. 3,674,893), it would be desirable to avoid the need for such additives and provide the impact resistance as an inherent property of the resin. Additives to any thermosettable resin frequently result in other problems such as instability, viscosity control and the like which can be avoided if the need for the additive can be eliminated in the first place.
Vinyl ester resins are generally prepared by reacting together about equivalent amounts of an unsaturated monocarboxylic acid and a polyepoxide. An early patent U.S. Pat. No. 3,179,623, describes the above reactions and resins. Further details about the resins, which are called vinyl ester resins herein, and conditions and methods of making them can be found in the following U.S. Pat. Nos.: 3,301,743; 3,317,465; 3,377,406; 3,256,226 and 3,367,992. All the above patents are incorporated herein by reference.
Briefly, any of the known polyepoxides may be employed in the preparation of the vinyl ester resins of this invention. Useful polyepoxides are glycidyl polyethers of both polyhydric alcohols and polyhydric phenols, flame retardant epoxy resins based on tetrabromo bisphenol A, epoxy novolacs, epoxidized fatty acids or drying oil acids, epoxidized diolefins, epoxidized diunsaturated acid esters as well as epoxidized unsaturated polyesters, so long as they contain more than one oxirane group per molecule. The polyepoxides may be monomeric or polymeric.
Preferred polyepoxides are glycidyl polyethers of polyhydric alcohols or polyhydric phenols having equivalent weights per epoxide group of about 150 to 1500, preferably about 250 to 700 and more preferred about 400 to 600. Generally, as the epoxide equivalent weight decreases the amount of carboxy terminated rubber increases. The polyepoxides are characterized by the presence of more than one epoxide group per molecule.
Unsaturated monocarboxylic acids include acrylic acid, methacrylic acid, halogenated acrylic or methacrylic acids, cinnamic acid and the like and mixtures thereof, and hydroxyalkyl acrylate or methacrylate half esters of dicarboxylic acids as described in U.S. Pat. No. 3,367,992 wherein the hydroxyalkyl group preferably has from two to six carbon atoms. Said acid is generally reacted with the polyepoxide in the proportions of about 1 equivalent of acid per each equivalent of epoxide, but the proportions of equivalents may range from about 0.8/1 to 1.2/1, respectively.
According to this invention improved impact resistance is obtained by replacing up to about 20 percent of the equivalents of unsaturated acid with an equivalent amount of a liquid carboxy terminated polydiene rubber. By liquid it is meant to include the low molecular weight polydienes of about 2000 to 20,000 molecular weight and preferably about 3,000 to 10,000. Of the combined acid equivalents employed in the process at least about 80 percent comprises said unsaturated acid and the balance between about 0.01 and 20 percent comprises said polydiene, provided that the polydiene rubber content of the resin is at least about 4 weight percent. By carboxy terminated is meant that the polydiene rubber is terminated at each end with an acid carboxy, --COOH, group.
The particular liquid carboxy terminated polydienes used in this invention may be prepared by any suitable means. One procedure involves solution polymerization of a conjugated diene monomer in the presence of an organo metal catalyst. The lithium catalysts and in particular the dilithium catalysts such as dilithiobutane, dilithium stilbene, dilithium napthalene and the like are preferred. By employing dilithium catalysts the polymer obtained is terminated at each end by a lithium atom. Treatment of said polymer with carbon dioxide replaces the lithium atoms with carboxy lithium salt groups. As a final step the polymer is treated with acid to convert the lithium salt to the free acid form. Carboxy terminated polymers of various conjugated dienes or mixtures of same may be prepared in this manner. The conjugated dienes may have from 4 to 12 carbon atoms and preferably from 4 to 8. Typical monomers include 1,3-butadiene, isoprene, piperylene, methylpentadiene, 3,4-dimethyl-1,3 hexadiene and the like.
Also included within the definition of polydiene rubbers are carboxy terminated liquid copolymers of a conjugated diene and a copolymerizable vinyl monomer. Suitable monomers include alkenyl aromatics such as styrene, vinyl toluene, α-methyl styrene etc.; nitriles such as acrylonitrile, methacrylonitrile, etc.; acrylate and methacrylate esters such as the methyl, ethyl, propyl, cyclohexyl etc. esters; heterocyclic nitrogen-containing monomers such as the various vinyl pyridine isomers, etc.; vinyl chloride, vinylidene chloride, methyl vinyl ether and the like. Said copolymers should contain at least 40 weight percent of diene and correspondingly from 0 to about 60 weight percent of at least one copolymerizable vinyl monomer different from said diene monomer.
Preferred copolymer polydienes are the liquid carboxy terminated acrylonitrile/butadiene copolymers and particularly preferred are those copolymers prepared from 12 to 25 percent acrylonitrile and 88 to 75 percent butadiene.
The preparation of carboxy terminated polydienes is well known. U.S. Pat. No. 3,135,716 is typical of the art describing a process for preparing terminally reactive polymers as well as the various reactions which may be employed to introduce different functional terminal groups. The disclosure of U.S. Pat. No. 3,242,129 is also typical of the art, especially the portions contained in columns 6-8 thereof. The above two patents are incorporated herein by reference. Numerous other patents could be cited but are considered unnecessary.
The vinyl ester resins typically are prepared in the presence of catalysts such as the organophosphonium salts, tertiary amines such as 2,4,6-tri(dimethylaminomethyl) phenol [DMP-30] and the like. Various vinyl polymerization inhibitors such as hydroquinone or its methyl ether and the like may be present during the reaction or added after the resin forming reaction. If desired the reaction may be run in an inert solvent, preferably one which can be readily removed by evaporation etc. after the resin has been prepared. The carboxy terminated polydiene may be reacted with the polyepoxide first followed by addition and reaction of the unsaturated monocarboxylic acid or both acid reactants may be added and reacted with the polyepoxide at the same time.
The polydiene rubber modified vinyl ester resin produced herein typically contains terminal polymerizable groups and associated therewith a hydroxyalkylene group, e.g. --CH2 CH(OH)CH2 --, formed by the reaction of the acid carboxy group with the epoxide group. This hydroxyl group may be used for further modification, e.g. by a post-reaction with a dicarboxylic acid anhydride in proportions up to about 1 mole per equivalent of hydroxyl. A modification of this kind is disclosed in U.S. Pat. No. 3,564,074. Other materials which are reactive with hydroxyl groups, e.g. isocyanates, acyl halides, etc. may be used to modify the vinyl ester resin.
Both saturated and unsaturated anhydrides are useful in said post reaction. Suitable dicarboxylic acid anhydrides containing ethylenic unsaturation include maleic anhydride, the halogenated maleic anhydrides, citraconic anhydride, itaconic anhydride and the like and mixtures thereof. Saturated dicarboxylic acid anhydrides include phthalic anhydride, tetrabromophthalic anhydride, chlorendic anhydride, anhydrides of aliphatic unsaturated dicarboxylic acid and the like.
The rubber modified vinyl ester resins are higher molecular weight resins by virtue of chemically combining the carboxy terminated polydiene rubbers into the resin structure. Accordingly, many of the resins are suitable as powder coating materials. A mixture of the powdered resin with a peroxide or other catalyst may be readily cured at an elevated temperature. The pendant carboxyl groups are of importance in powder coatings since they can be reacted with metal oxides to make solid powdered even in the presence of liquid monomers.
The resins are more commonly used in admixture with a copolymerizable monomer to prepare laminates, glass reinforced plastic pipe, reinforced molded parts, and the like. The rubber modified vinyl ester resin may be combined with up to 60 to 70 weight percent of monomer. The proportions will vary, somewhat depending on the monomer selected, other additives employed and other factors. A variety of copolymerizable monomers are disclosed in the vinyl ester patents previously referred to. Typical monomers are styrene, vinyl toluene, halogenated styrenes, alkyl substituted styrenes, alkyl substituted styrene, acrylic and methacrylic esters, hydroxyalkyl esters of acrylic and methacrylic acid, and the like. More usually the monomer content will range from about 30 to 60 weight percent.
The choice of monomer is also based on whether the resin is to be cured by thermal and/or chemical means or by high energy radiation. With chemical catalysts (e.g. peroxides, persulfates, diazo compounds, etc.) and/or heat styrene is a common monomer because of its low cost and availability as well as the properties obtained. However, to minimize the radiation dosage needed to cure monomers other than aromatic monomers may be employed such as butyl acrylate and hydroxyalkyl acrylates.
As indicated, the rubber modified vinyl ester resin may be cured (thermoset) by various means. Cure accelerators such as the metal organic acid salts, e.g. cobalt naphthenate, or tertiary amines such as N,N-dimethyl toluidine are frequently used with chemical catalysts. Sensitizers or photoinitiators which reduce the radiation dosage may also be employed with radiation, especially with ultra violet light. Other materials may be added to the resin such as inert reinforcing fibers, e.g. glass, asbestos, carbon, etc.; inert fillers such as kaolin clay, CaCO3 etc.; mold release agents, thickeners, other pigments, thermoplastic low-profile additives, density reducers such as glass or phenolic microballons, blown saran microspheres and the like.
The improved impact resistance of the rubber modified vinyl ester resins makes the resin especially useful in coatings and for molded articles. Of particular interest are molded parts such as motor housings for power mowers, boats and recreation products, automotive parts such as panels and housings, molded furniture containing blown saran microspheres where improved toughness and durability are required in medium density syntatic foams for chair legs and arms, doors, backup for acrylic faced bath tubs, lavatories, etc.
The invention will be further illustrated by the following non-limiting examples. All parts and percentages are by weight unless otherwise specified.
EXAMPLE 1
In a suitable reactor 455 parts of a glycidyl polyether of bisphenol A having an epoxide equivalent weight (EEW) of 189 (D.E.R.331) was reacted with 154 parts of bisphenol A in the presence of 0.5 part of t-butyl phosphonium acetate at 150° C. The reaction exothermed to 190° C. and yielded a polyepoxide resin with an EEW of about 600.
After cooling the following were added to the reactor: 76 parts methacrylic acid, 1.2 parts DMP-30 catalyst, 228 parts carboxy terminated copolymer of butadiene-acrylonitrile (82:18) containing 2.5% carboxy, --COOH(Hycar CTBN, Goodrich Chemical Co.) and 0.17 part of hydroquinone. The reaction was continued at 120°-130° C. until the percent carboxy of the resin was 1.15%. The resin was then poured out in thin sheets to cool. This resin contained about 25% of said rubber. Additional resins containing decreasing amounts of said rubber were prepared in a similar manner, substituting an equivalent amount of methacrylic acid for the amount of the decrease in rubber content. A portion of each of the resins was powdered, mixed with 1% dicumyl peroxide, cured at 280° F. and post-cured at 100° C. for 30 minutes. A control resin with no rubber was made for comparison purposes.
______________________________________                                    
       %        Heat Distortion                                           
                             Notched Izod Impart,                         
Resin  Rubber   264 psi      Ft-lb/inch                                   
______________________________________                                    
A      0        184          0.3                                          
B      5.8      176          0.4                                          
C      11.1     166          0.4                                          
D      15.7     157          0.5                                          
E      25       140          1.02                                         
______________________________________
As noted each of the uncured resins was non-blocking at 70° F. and could be powdered or flaked. Similar results are obtained if the copolymer is replaced by an equivalent amount of a carboxy terminated polybutadiene.
Tests were also made with some of the resins diluted to 50% styrene monomer. Clear castings were made by adding 1% benzoyl peroxide, curing at 100° C. for 1 hour and post-curing at 130° C. for 45 minutes.
__________________________________________________________________________
         Izod Notched                                                     
    Visc.,*                                                               
         Impact %   HDT, °F.                                       
                          Tensile                                         
                              Flex. Str                                   
                                   Flex Mod                               
Resin                                                                     
    cps  Ft-lbs/in.                                                       
                Elong.                                                    
                    264, psi                                              
                          psi psi  psi × 10.sup.5                   
__________________________________________________________________________
A    300(N)                                                               
         0.380   9  215   11,000                                          
                              17,300                                      
                                   4.3                                    
D   2000(T)                                                               
         0.595  25  174   7,170                                           
                              11,900                                      
                                   3.2                                    
E   2600(T)                                                               
         0.563  25  124   4,000                                           
                               5,700                                      
                                   2.1                                    
__________________________________________________________________________
 *N--newtonian;                                                           
 T--thixotropic
Additional tests were made with resin E in which an unmodified vinyl ester resin (prepared by reacting equivalent amounts of an epoxy novolac, D.E.N. 438, with methacrylic acid) diluted to 25% styrene was blended therewith in varying amounts to vary the amount of rubber in the total resin. Clear castings were then made by curing with 1% benzoyl peroxide (BPO) at 80° C. for 6 hours and post curing for 30 minutes at 250° F. The casting at a 10% rubber level could be hammered and was slightly malleable whereas at 2.5% rubber the castings were brittle and shattered easily.
EXAMPLE 2
Similar to example 1 a higher molecular weight polyepoxide was first prepared by reacting 6.5 lbs of bisphenol A with 6.58 lbs of D.E.R. 736 (an aliphatic diepoxide with an EEW of 175-205) in the presence of t-butyl phosphonium acetate catalyst. Then 4.05 lbs of a carboxy terminated butadieneacrylonitrile rubber similar to example 1, 6.97 lbs of methacrylic acid were added and reacted using a catalyst (DMP-30) and hydroquinone as an inhibitor. After the reaction was completed 36 lbs of styrene was added and mixed with the resin. The liquid resin had a viscosity of 57.7 cs.
The following molding formulation was prepared.
______________________________________                                    
Resin                   100    parts                                      
Nevada sand             37.5   parts                                      
Milled glass fiber      25     parts                                      
ASP-400 Kaolin clay     12.5   parts                                      
Cab-O-Sil (silica)      0.5    parts                                      
N,N--dimethylaniline (DMA)                                                
                        0.4    parts                                      
Cadox 40E (40% benzoyl)                                                   
peroxide                5.0    parts                                      
______________________________________
A pipe collar was molded directly into a 12 inch pipe using the above formulation at 150° F. The collar was demolded about 15 minutes after the formulation was accelerated with the DMA promoter. The collar was aged for 24 hours and then tested for impact resistance. The collar passed a 20 foot drop test without breaking.
Clear castings were also prepared from the resin using two different catalyst systems.
______________________________________                                    
        1% benzoyl peroxide                                               
                      0.5% Co Naph                                        
        0.2% DMA      1.5% MEK Peroxide                                   
______________________________________                                    
Tensile, psi                                                              
          6,820           5,940                                           
Elongation, %                                                             
            15              38                                            
264 psi, HDT                                                              
          120° F.  --                                              
______________________________________
EXAMPLE 3
Another group of resins was prepared by heating together in the presence of a catalyst a polyepoxide or mixtures thereof, methacrylic or acrylic acid and a carboxy terminated butadiene/acrylonitrile rubber similar to that used in example 1. Heating was continued until the carboxy content reached a low value of less than 2%. Styrene monomer was then added. Clear castings were cured with 1% BPO and 0.2% DMA for one hour at 80° C. and post cured at 250° C. for 1 hour. The compositions of the resins and their physical properties are recorded in the following tables.
__________________________________________________________________________
Composition                                                               
                                  Rubber                                  
Resin                                                                     
    D.E.R. 331.sup.(1)                                                    
           D.E.R. 732.sup.(2)                                             
                  D.E.R. 741.sup.(3)                                      
                         MAA.sup.(4)                                      
                              AA.sup.(4)                                  
                                  Parts                                   
                                      %  Styrene                          
__________________________________________________________________________
A   760    --     --     --   288 112 7  500                              
B   570    325    --     335  --  140 7  590                              
C   570    325    --     335  --  310 14 660                              
D   570    --     370    335  --  145 7  610                              
E   570    325    --     335  --   0  0  530                              
__________________________________________________________________________
 .sup.(1) aromatic polyepoxide, EEW 186-192                               
 .sup.(2) aliphatic polyepoxide, EEW 305-335                              
 .sup.(3) mixture of aromatic and aliphatic polyepoxide, EEW 364-380      
 .sup.(4) MAA--methacrylic acid;                                          
 AA--acrylic acid                                                         

______________________________________                                    
Properties                                                                
Izod Impact      Flexural                                                 
Ft-lbs/inch      Strength,                                                
                          Barcol   HDT, °F.                        
Resin Unnotched Notched  psi    Hardness                                  
                                       264 psi                            
______________________________________                                    
A     3.5       0.207    13,000 24     167                                
B     7.7       0.422     9,000 23     149                                
C     10.5      0.552     4,500  0     --                                 
D     7.2       --       11,300 27     167                                
E     4.7       0.141    15,000 40     177                                
______________________________________
EXAMPLE 4
Variations in the previous examples may be made. The procedure of example 1 was changed by reacting the polyepoxide, the polydiene rubber and the bisphenol A together first at 140°-160° C. After cooling to 110° C. the methacrylic acid was added and reacted. The epoxy and the rubber may be combined first and heated followed by addition of the bisphenol A and heating until desired epoxide equivalent weight is produced. Other polyepoxides which were used in the preparation of the vinyl ester resins of this invention included an epoxy novolac (D.E.N. 431) with an EEW of 172-179 and flexible polyepoxides with an EEW of 305-335 (D.E.R. 732) and 364-380 (D.E.R. 741). The CTBN rubbers may be replaced by an equivalent amount of any of the commercial carboxy rubbers such as Butarez CTL I and II (Phillips Petroleum), Telogen CT (General Tire & Rubber Co.) or HC-434 (Thiokol Chemical Co.).
EXAMPLE 5
The polydiene rubber modified vinyl ester resins have improved adhesive properties as well as impact resistance. Resins A, D and E of example 1 were used. In addition Resin A (0% rubber) was physically blended with the polydiene rubber used in preparing Resin D and E to a 12.5% rubber level. All resins were diluted to 50% styrene.
An adhesive formulation with each resin was prepared by blending 20 parts per 100 parts of resin (phr) of MD-101 aluminum powder and 1 phr benzoylperoxide. Lap shear specimens were prepared according to ASTM-1002 using chromate etched aluminum strips, 1×4×0.064 inches. The adhesives were cured at 250° F. for 30 minutes and after cooling lap shear values were determined.
______________________________________                                    
            Percent Polydiene                                             
                         Lap Shear                                        
Resin       Rubber       psi                                              
______________________________________                                    
1,A         0            3270                                             
1,D         7.7          4980                                             
1,E         12.5         3635                                             
Blend*      12.5          325                                             
______________________________________                                    
 *Blend of rubber and Resin 1,A.
The improvement is apparent and is particularly evident over the blended resin where the added rubber detracted from the lap shear value.
EXAMPLE 6
Carboxy rubber modified vinyl ester resins were compared to comparable resins without said rubber. McGarey cleavage tests were made by preparing test bars 6×1.2×0.25 inches in which a lengthwise cut was made on each side of the bar to one-third the thickness of the bar. At one end an initial 1 inch cut was made all the way through the bar to help initiate splitting. In each case the resin was cured with 1% benzoyl peroxide catalyst for 6 hours at 80° C. followed by 45 minutes at 250° F.
The test bars were then split the length of the cut obtaining a stress-strain curve. Stress was applied at a rate of 0.05 inches per minute. The area under the plotted curve was taken to be representative of the work required to form the new split surface. At the same styrene level the test bar with no rubber content in the resin had an area under the stress-strain curve of 190 whereas the carboxy polydiene rubber containing resin had an area of 2350. The split in the latter case also showed a great deal of stress whitening along the crack propagation line which is an indication of toughness.

Claims (16)

What is claimed is:
1. A process for preparing a thermosettable resin having improved impact resistance in the thermoset state which comprises .[.simultaneously.]. reacting the epoxide moieties of a polyepoxide having an average of more than one epoxide group per molecule with the acid moieties of an unsaturated monocarboxylic acid and a liquid carboxy terminated polydiene rubber wherein the combined acid equivalents of said unsaturated acid and said polydiene ranges from about 0.8 to 1.2 equivalents per epoxide equivalent and wherein at least about 80 percent of said acid equivalents comprises said unsaturated acid and the balance between 0.01 and 20 percent comprises said polydiene, provided that the polydiene rubber content is at least about 4 weight percent .Iadd.and wherein said resin is prepared by the simultaneous reaction of said polyepoxide, said polydiene rubber and said monocarboxylic acid or by the sequential reaction wherein said polyepoxide and said polydiene rubber are reacted followed by addition and reaction of said monocarboxylic acid with the product of that first reaction.Iaddend..
2. The process of claim 1 wherein said polydiene rubber has a molecular weight of 2,000 to 20,000.
3. The process of claim 1 wherein said polydiene rubber molecular weight is 3,000 to 10,000.
4. The process of claim 1 wherein said polydiene rubber is a polymer of a conjugated diene monomer.
5. The process of claim 1 wherein said polydiene rubber is a copolymer of a conjugated diene and a copolymerizable vinyl monomer.
6. The process of claim 1 wherein said polydiene rubber is a copolymer of acrylonitrile and butadiene.
7. The process of claim 1 wherein said polyepoxide has an epoxide equivalent weight of 250 to 700.
8. The process of claim 1 further comprising the step of admixing the thermosettable resin with a copolymerizable monomer.
9. A thermosettable resin prepared by the process of claim 1.
10. A thermosettable resin prepared by the process of claim 2.
11. A thermosettable resin prepared by the process of claim 3.
12. A thermosettable resin prepared by the process of claim 4.
13. A thermosettable resin prepared by the process of claim 5.
14. A thermosettable resin prepared by the process of claim 6.
15. A thermosettable resin prepared by the process of claim 7.
16. A thermosettable resin prepared by the process of claim 8.
US06/124,055 1973-03-21 1980-02-25 Impact resistant vinyl ester resin and process for making same Expired - Lifetime USRE31310E (en)

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US343716A US3892819A (en) 1973-03-21 1973-03-21 Impact resistant vinyl ester resin and process for making same
NL7508905A NL7508905A (en) 1973-03-21 1975-07-25 PROCESS FOR PREPARING A THERMO-HARDENING RESIN.
FR7523452A FR2319656A1 (en) 1973-03-21 1975-07-28 PROCESS FOR PREPARATION OF THERMOSETTING RESINS
JP50092437A JPS5216598A (en) 1973-03-21 1975-07-29 Process for preparing thermosetting resin
DE19752534037 DE2534037A1 (en) 1973-03-21 1975-07-30 METHOD FOR THE MANUFACTURING OF THERMAL RESIN
BR7504875A BR7504875A (en) 1973-03-21 1975-07-30 PROCESS TO PREPARE A THERMOFIXABLE RESIN
US06/124,055 USRE31310E (en) 1973-03-21 1980-02-25 Impact resistant vinyl ester resin and process for making same

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3512791A1 (en) * 1984-04-11 1985-10-24 Matsushita Electric Works, Ltd., Kadoma, Osaka RUBBER-MODIFIED VINYL ESTER AND THESE-CONTAINING, HEAT-RESISTANT RESIN COMPOSITION
EP0292219A3 (en) * 1987-05-21 1989-10-11 AT&T Corp. Printed circuit board fabrication
US5095046A (en) * 1990-02-06 1992-03-10 Exxon Chemical Patents Inc. Hot melt adhesive of ethylene/unsaturated acid copolymer and epoxy crosslinker
US5198510A (en) * 1990-04-27 1993-03-30 The B. F. Goodrich Company Modification of vinyl ester resins with reactive liquid polymers
US5242980A (en) * 1990-02-06 1993-09-07 Exxon Chemical Patents Inc. Ethylene-unsaturated alcohol or acid copolymer and epoxy crosslinker
US20020111311A1 (en) * 2000-12-18 2002-08-15 Chandrika Govardhan Daptomycin and related analogs in crystalline form

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3674893A (en) * 1969-04-01 1972-07-04 Dow Chemical Co Thermosettable resins containing vinylester resin,polydiene rubbers and vinyl monomers
US3808114A (en) * 1970-09-14 1974-04-30 Showa Highpolymer Light-curable polyglycidyl ester compositions

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3674893A (en) * 1969-04-01 1972-07-04 Dow Chemical Co Thermosettable resins containing vinylester resin,polydiene rubbers and vinyl monomers
US3808114A (en) * 1970-09-14 1974-04-30 Showa Highpolymer Light-curable polyglycidyl ester compositions

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3512791A1 (en) * 1984-04-11 1985-10-24 Matsushita Electric Works, Ltd., Kadoma, Osaka RUBBER-MODIFIED VINYL ESTER AND THESE-CONTAINING, HEAT-RESISTANT RESIN COMPOSITION
DE3512791C2 (en) * 1984-04-11 1998-09-17 Matsushita Electric Works Ltd Insulating plate
EP0292219A3 (en) * 1987-05-21 1989-10-11 AT&T Corp. Printed circuit board fabrication
US5095046A (en) * 1990-02-06 1992-03-10 Exxon Chemical Patents Inc. Hot melt adhesive of ethylene/unsaturated acid copolymer and epoxy crosslinker
US5242980A (en) * 1990-02-06 1993-09-07 Exxon Chemical Patents Inc. Ethylene-unsaturated alcohol or acid copolymer and epoxy crosslinker
US5198510A (en) * 1990-04-27 1993-03-30 The B. F. Goodrich Company Modification of vinyl ester resins with reactive liquid polymers
US20020111311A1 (en) * 2000-12-18 2002-08-15 Chandrika Govardhan Daptomycin and related analogs in crystalline form

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