CA2071044C - Stabilization of polyesters using epoxy compounds in combination with a catalyst - Google Patents

Abstract

A novel polyester composition is disclosed comprising a linear polyester resin, a difunctional epoxy compound and a catalyst. The novel polyester compositions have excellent melt viscosity properties including excellent retention of melt viscosity after aging.

Description

STABILIZATION OF POLYESTERS USING EPOXY COMPOUNDS IN
COMBINATION WITH A CATALYST
CROSS REFERELJCE Tn 1~121'.nTrrT~ nfl~r.rr~~~rrm,Te The present invention is related to Canadian Patent Application Serial No. 2,071,012, filed June 11, 1992, entitled Stabilization of Mineral Filled Polyesters Using Epoxy Compounds.
FIELD O ' The present invention relates to polyester camnpositioas.
More particularly the present invention relates to polyester camnpositions having inoproved hydrolytic stability and melt viscosity stability. Most particularly, the present invention io relates to linear polyester resins stabilized with epoxy comnpounds in comnbination with a catalyst.
Linear polyesters, such as polyethylene terephthalate) or PET, and poly(butylene terephthalate) or PBT, are widely used in 15 the preparation of articles by forming methods such as injection molding and tube extrusion. Many of their properties, including chemnical stability, solvent resistance and low permeability to gases, make theme attractive candidates for such forming operations as blow adding, profile extrusion and theraroforming.
2o One problem in such operations is the relatively low melt viscosities of the polyesters, as a result of which the formed articles do not adequately retain their shape iaenediately after forming and before they have cooled.
In recent years, various methods have been developed for z5 increasing the melt viscosities and melt strengths of such polyesters.

336-2281(8CV-5313) Rodama-et al., Unit~d States Patent No. 4,141,882, describe obtaining a polyester composition having high melt viscosity by blending a polyester comprising at least 80 mole percent of ethylene terephthalate units with (1) an epoxy compound of isocyanuric acid construction (A) and at least one organic compound (B) capable of reacting with the epoxy compound (A), or (2) a product of the melt reaction of epoxy compound (A) with the organic compound (H).
Blaschke et al., United Kingdom Patent No. 2,098,231 describe shaped bodies formed of polytetramethylene terephthalate stabilized with triglycidyl isocyanurate (TGIC) or a bisoxazoline.
Yosihara, United States Patent No. 4,795,771, describes polyesters exhibiting crystallization at low temperatures and having high heat distortion temperatures and good dimensional stability. The disclosed polyester compositions consist of polyester, of which 80~ is polyethylene terephthalate), a carboxylic acid ester of a polyalkylene glycol, an epoxy compound having a polyoxyalkylene and an inorganic filler such as talc.
Rawlings, United States Patent No. 4,533,679, describes reinforced polyesters consisting of a polyester resin, a polyepoxy having more than two epoxide functionalities and a reinforcing agent.
Borman et al., United States Patent No. 4,020,IZZ, describe a method to increase the melt elasticity or viscosity of linear high molecular weight polyesters. The patentees teach adding to the polyester organic polyepoxides having at least two epoxide groups per molecule.
Rower, United States Patent No. 4,071,504, disclose low carboxyl content polyester fibers. The fibers are produced by melt extruding a polyester and a catalytic material, such as an alkali metal salt, and adding and reacting therewith monofunctional epoxidss.
Brown et al., United States Patent No. 4,904,746, teach producing branched polyesters having advantageous melt viscosity properties. The improved method comprises forming a reactive concentrate by reacting (A) triglycidyl isocyanurate with (B) a linear polymer having ester and free carboxylic groups. The reactive concentrate is then melt blended with (C) a linear polyester with free carboxylic groups.
McCracken et al., United States Patent No. 4,933,429, teach the production of high melt viscosity branched polyesters. The disclosed branched polyesters are produced by effecting a reaction between (A) a polyester having a substantial portion of free carboxylic groups, (B) a polyepoxy comnpound, preferably having at least three epoxy functionalities, and (C) a catalyst selected from salts of aliphatic io carboxylic acids and prianary alkylamines.
Ko~netani et al., United States Patent No. 4,246,378, further describe a polyester having improved melt stability. The patentees teach preparing a cam~ositian having 100 parts by weight of polyester, 0.1 - 40 parts by weight of an epoxy compound, and 0.001 - 10 parts by weight of organic sulfonate salts and organic sulfate salts.
Borman et al., United States Patent No. 3,886,104, teaches stabilizing high molecular weight polyester resins by adding to the polyester resin a stabilizer ca~rising an internally polyfunctional epoxide having at least two epoxide functionalities. The epoxide 2o containing stabilizers disclosed to be useful are epoxidized polyunsaturated triglycerides.
Commn~only assigned Canadian Patent Application Serial No.
2,039,832, filed April 4, 1991 discloses branched polyesters having enhanced melt viscosity. The application describes adding a reinforcing mineral to a polyester resin branched with a TGIC branching agent.
Hor~ever, the above-described polyester compositions still suffer from processing drawbacks at high melt viscosities. This processability difficulty resulted frc~n melt stiffness encountered when larger amounts of poly~epoxide functional agents were em~i~ployed. Thus, there exists in 3o the art a need for high melt viscosity linear polyester resins which are easily processable.
Surprisingly, it has now been found that compositions comprising linear polyesters, difunctional epoxides and salts of aliphatic carboxylic acids provide a campositi~ which possesses 4 336-2281(8CV-5313) both excellent hydrolytic stability and melt viscosity stability.
Further, preferred polyester compositions possess high melt viscosity and ease of processability. The compositions of the present invention unexpectedly exhibit improved results over compositions employing mono- and tri- functional epoxides.
It is further noteworthy that while compositions containing linear polyesters and branched polyesters have good hydrolytic stability, surprisingly the linear polyester compositions of the present invention are better than the branched in this respect.
StJM~ARY OF T8~ IHVENTI0~1 According to the present invention there is provided a thermoplastic resin composition comprising (a) a linear polyester.
res in; ( b ) a d3 functional polyepoxy compound; and ( c ) a catalyst.
Preferably the compositions of the present invention further comprises (d) a hindered phenol antioxidant.
Preferably the polyester component (a) is selected from the group consisting of poly(1,4-butylene tarephthalate), polyethylene twrephthalate), poly(1,4-cyclohexanedimethanol terephthalate) and blends of any of the foregoing, and is present in an amount ranging from about 60 to about 100 weight percent based on the weight of the total composition.
The preferred difunctional polyepoxy compound (b) is 3,4 epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylata. The preferred catalysts (c) are salts of an aliphatic carboxylic acid. The most preferred catalyst (c) is sodium stearate.
Also according to the present invention there is provided a method for improving the melt viscosity of a linear polyester resin comprising compounding with a linear polyester resin an effective amount of a difunctional polyepoxy compound and an effective amount of a salt of an aliphatic carboxylic acid.
Further, according to the present invention, there are provided articles made from the polyester compositions of the present invention.

336-2281(8CV-5313) DETAILED DESCRIPTION OF THE PRESENT INVENTION
Component (a) of the present invention comprises linear polyester resins. Polyesters generally for use herein are derived from an aliphatic or cycloaliphatic diol, or mixtures 5 thereof, containing from Z to about 10 carbon atoms and at least one aromatic dicarboxylic acid. Preferred polyesters are derived from an aliphatic diol and an aromatic dicarboxylic acid and have repeating units of the following general formula -f- CIi=--~- O _ C
wherein n is an integer of from 2 to 6. The most preferred polyesters are polyethylene tsrephthalate), poly(1,4-butylene terephthalate) and mixtures thereof.
Also contemplated herein are the above polyesters with minor amounts, e.g., from 0.5 to about 5 percent by weight, of units derived from aliphatic acids and/or aliphatic polyols to form copolyestera. The aliphatic polyols include glycols, such as poly(ethylsne glycol). All such polyesters can be made following the teachings of, for example, United States Patent Nos.
2,465,319 and 3,047,539.
The polyesters which ate derived from a cycloaliphatic diol and an aromatic dicarboxylic acid are prepared, for example, by condensing either the cis- or traps- isomer (or mixtures thereof) of, for example, 1,4-cyclohexanedimethanol with and aromatic dicarboxylic acid so as to produce a polyester having recurring units of the following formula -O-CH= CHi O-C~R-C-wherein the cyclohsxane ring is selected form the cis- and trans-isomers thereof and R represents an aryl radical containing 6 to 20 carbon atoms and which is the decarboxylatad residue derived from an aromatic dicarboxylic acid.

6 336-ZZ81(8CV-5313) Examples of aromatic dicarboxylic acids represented by the decarboxylated residue R are isophthalic or terephthalic acid, l,Z-di-(p-carboxyphenyl)ethane, 4,4'-dicarboxydiphenyl ether, etc., and mixtures of these. All of these acids contain at least one aromatic nucleus. Acids containing fused rings can also be present, such as in 1,4- or 1,5-naphthalenedicarboxylic acids.
The preferred dicarboxylic acids are terephthalic acid or a mixture of terephthalic and isophthalic acids.
Another preferred polyester may be derived from the reaction of either the cis- or traps- isomer ( or a mixture thereof ) of 1,4-cyclohexanedimethanol with a mixture of isophthalic and terephthalic acids. Such a polyester would have repeating units of the fonaula O
i~
O ~ C ..
- O- CH= CHi O - C
Still another preferred polyester is a copolyester derived from a cyclohexanedimethanol, an alkylene glycol and an aromatic dicarboxylic acid. These copolyesters are prepared by condensing either the cis- or traps- isomer (or mixture thereof) of, for example, 1,4-cyclohexanedimethanol and an alkylene glycol with an aromatic dicarboxylic acid so as to produce a copolyester having units of the formulae : .

i~ n -(- O- CHz CH= O -C ~ R- C

n -t-O --~-CHi-~- O -C -R-C
wherein the cyclohexane ring is selected from the cis- and trans-isomers thereof, R is as previously defined, n is an integer of 2 to 6, the x units comprise from about 10 to about 90 percent by weight and the y units comprise from about 90 to about 10 percent by weight.
Such a preferred copolyester may be derived from the reaction of either the cia- or traps- isomer (or mixtures 20'1044 ,.~..

7 336-2281(SCV-5313) thereof) of 1,4-cyclohexansdimethanol and ethylene glycol with terephthalic acid in a molar ration of 1:2:3. These copolyesters have repeating units of the following formulae 0 _ 0 --~ O - CHi CH=- O -C ~ ~ C -~-O .. O
--~- O -.ECHi-~- 0 - C
wherein x and y era as previously defined.
The polyesters described herein are either commercially available or can be produced by methods well known in the art, such as those set forth in, for example, United States Patent No.
2,901,466.
The polyesters used herein have an intrinsic viscosity of from about 0.4 to about 2.0 dl/g as measured in a 60:40 phenol/tetrachloroethane mixture or similar solvent at 23° - 30°
C.
The polyester resin component can vary widely in amount.
Preferably the polyester resin component is present in an amount ranging from about 60 to about 100 weight percent based on the total weight of the composition. More preferably the polyester resin component is present in an amount ranging from about 90 to about 100 weight percent based on the total weight of the composition. Where a blond of polyethylene terephthalate) and poly(1,4-butylene tsraphthalate) is employed, the polyester resin component will comprise from about 1 to about 99 parts by weight polyethylene terephthalate) and from about 99 to about 1 part by weight poly(1,4-butylene tersphthalate) based on 100 parts by weight of the polyethylene terephthalate) and poly(1,4-butylene terephthalate) combined. However, other polyester blends are also contemplated within the scope of the present invention.
Component (b) is at least one difunctional epoxy compound.
By difunctional epoxy compound is meant a compound having two terminal epoxy functionalities. Preferably the compound will contain only carbon, hydrogen and oxygen. The compound will preferably have a molecular weight of below about 1000, to 20'1044 8 336-2281(8CV-5313) facilitate blending with the polyester resin. Preferred difunctional epoxy compounds will have at least one of the epoxide groups on a cyclohexane ring. Examples of preferred difunctional epoxy compound: are 3,4-epoxycyclohaxyl-3,4-epoxycyclohexylcarboxylate, bis(3,4 epoxycyclohexylmethyl)adipate, vinylcyclohexene di-epoxide, bisphenol diglycidyl ethers, diglycidyl adducts of amines and amides, diglycidyl adducts of carboxylic acid: and the like.
Especially preferred is 3,4-epoxycyclohexyl-3,4 epoxycyclohexylcarboxylate.
The difunctional epoxide compounds can be made by techniques well known to those skilled in the art. For example, the corresponding a,8-dihydroxy compounds can be dehydrated .to produce the epoxide groups, or the correspondingly unsaturated' compounds can be epoxidized by treatment with a peracid, such as peracetic acid, in well-known techniques. The compounds are also commercially available.
The difunctional epoxy compound may be employed in any effective amount, but preferably small amounts are use, e.g., at a range of about 0.1 to about 5 percent by weight. However, a particularly preferred range is from about 0.1 to about 3.5 percent by weight. A more preferred range is from about 0.5 to about 2 percent by weight. Within this particularly preferred range it has been found advantageous to employ in certain compositions from about 1 to about 1.5 percent by weight of the difunctional polyepoxy compound. All percentages are based on the combined weights of polyester component and the organic difunctional epoxide component.
Component (c) of the present invention consists of the catalyst compound. Preferred catalysts are salts free from direct carbon-phosphorous bond: and containing at least one of alkali metal cations and alkaline earth metal cations and halide anions. It is apparent that this class contains a large number of compounds. They include alkali metal halides, alkali m~tal carboxylates, alkali metal enolates, amine hydrohalidss, alkali metal carbonates and quaternary ammonium halides. illustrative compounds within this class are lithium fluoride, lithium iodide, ,,,., 9 336-2281(8CV-5313) potassium bromide, potassium iodide, sodium dihydrogen phosphate, sodium acetate, sodium benzoate, sodium caproate, sodium stearate, sodium ascorbate and dodecyltrimethylammonium bromide.
Salts of aliphatic carboxylic acids containing at least about 18 carbon atoms, especially the alkali metal stearates and preferably sodium stearate, have certain advantages over the other catalysts employed according to the invention and are therefore often preferred. In the first place, their use permits extrusion of the polyester-difunctional epoxide composition at substantially higher feed rates than those which are effective in their absence. in the second place, they tend to suppress the fortaation of acrolein, a by-product from glycidyl reagents. In the third place, they impart substantially less odor to the composition than certain other compounds useful as catalysts, especially amines.
The catalyst component can be present in the composition of the present invention in any effective amount. Preferably the catalyst is present in an amount ranging from about 0.01 to about 1 weight percent, more preferably from about 0.03 to about 0.1 weight percent based on the total weight of the resin composition.
Optionally, the present invention further comprises component (d) a hindered phenol thermal antioxidant. Any hindered phenol known to those skilled in the art may be employed herein, a wide variety of these are commercially available.
Hindered phenols will generally be of the type in which there is a sterically hindered phenolic group, especially one containing a t-butyl group in the ortho position to the phenolic OH group. Examples of such compounds are many. Preferred examples are, tetrakis (m~thylene-3-(-3',5'-di-tart-butyl-4'-hydroxyphenyl)-propionate)methane; octadecyl-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)propionate; 1,3,5-trimethyl-2,4,6-tris(3,5-di-tart-butyl-4-hydroxybenzyl)benzene; 4,4'-(2,2-diphenylpropyl)-diphenylamine; esters of ethoxylated aryl phenols; 2,2'-thiodiethylbis(3-(3,5-di-tert-butyl-4-hydroxyphenyl))propionate; octadecyl-3,5-di-tart-butyl-4-hydroxyhydrocinnamate and mixtures of any of the foregoing. Most zo~io44 336-2281(8CV-5313) preferred is octadecyl-3,5-di-tart-butyl-4-hydroxyhydrocinnamate, which is commercially available as "IRGANOX" 1076.
The compositions of the present invention can also comprise any number of conventional additives, such as dyes, pigments, 5 stabilizers, plasticizers, reinforcers, flame retardants, drip retardants, nucleants, rubbery impact modifiers and the like.
These are added, as desired, for their conventionally employed purposes. Illustrative flame retardant additives are disclosed in United States Patent Nos. 3,833,685; 3,342,254; 3,915,926 and 10 3,671,487. Other flame retardants are disclosed in United States Patent Nos. 3,681,281; 3,557,053; 3,830,771 and United Kingdom Patent No. 1,358,080.
Generally speaking, the more important of the flame retardant compounds contain chemical elements employed for their.
ability to impart flame resistance, e.g., bromine, chlorine, antimony, phosphorous and nitrogen. It is preferred that the flame-retardant additive comprise a halogenated organic compound (brominated or chlorinated); a halogenated-containing organic compound in admixture with a phosphorous compound or compounds containing phosphorous-nitrogen bonds or a mixture of two or more of the foregoing.
The amount of flame retardant additive used is not critical to the present invention, so long as it is present in minor proportion based on said composition, major proportions will detract from physical properties, but at least sufficient to render the polyester resin non-burning or self-extinguishing.
Those skilled in the art are well aware that the amount will vary ' with the nature of the resin and with the efficiency of the additive. In general, however, the amount of the additive will be from 0.5 to 50 parts by weight per 100 parts of resin.
A preferred range will be from about 3 to about 25 parts and an especially preferred range will be from about 8 to about 12 parts of flame retardant additive per 100 parts of resin.
Smaller amounts of compounds highly concentrated in the elements responsible for flame-retardance will be sufficient, e.g., elemental red phosphorous will be preferred at 0.5 to 2.0 parts by weight per hundred parts of resin, while phosphorous in the ~0~.~044 11 336-2281(8CV-5313) form of triphanyl phosphate will be used at 25 parts of phosphate per 100 parts of resin, and so forth. Iialogenated aromatics will be used at 8 to 12 parts and synergists, e. g. , antimony oxide, will be,used at about 2 to about 5 parts by weight per 100 parts by weight of resin.
The compositions of the present invention may also comprise a drip retardant agent. These are described in United States Patent No. 3,671,487. Generally, the drip retardant agent comprises a polytetrafluoroethylene resin, which is commercially available or can be prepared by known processes. They are white solids obtained by polymerization of the tetrafluoroethylene in aqueous media with free radical catalysts, e.g., sodium, potassium or ammonium peroxydisulfates at 100 to 1,000 psi and at 0 - 200°C and preferably 20 - 100°C. See, Hrubaker, United States Patent No. 2,393,967.
Preferred among the reinforcing agents are minerals such as mica, asbestos, wollastonite, clay, talc, carbon, ceramic, titanate, and mixtures thereof. Talc is especially preferred.
A moat preferred reinforcing agent comprises glass fillers.
Preferably the glass fillers are in the form of filamentous glass fibers or glass fla7ces. These are well known to those skilled in the art and are widely available from a number of manufacturers. For compositions ultimately employed for electrical uses, it is preferred to use fibrous glass filaments comprised of lime-aluminum borosilicate glass that is relatively sodium free. This is known as "E" glass. However, other glass compositions are useful. Especially preferred are .R filament glass (about 14 micron diameter), G filaatent glass (about 10 micron diameter) and D filament glass (about 7 micron diameter).
All such glasses are contemplated as within, the scope of the present invention. The filaments are made by standard processes, e.g., by steam or air blowing, flame blowing and mechanical pulling. The preferred filaments for plastics reinforcement are made by mechanical pulling. The filament diameters preferably range from about 0.00012 to about 0.00075 inch, but this is not critical to the present invention. It.is known, however, to those skilled in the art, that smaller filament diameters will 20'1044 12 336-2281(8CV-5313) also increase the strength of plastics treated therewith.
The length of the glass filaments and whether or not they are bundled into fibers and the fibers bundled in turn to yarns, ropes or rovings, or woven into mats, and the like are also not critical to the invention. However, in preparing the molding compositions of the present invention, it is convenient to use filamentous glass in the form of chopped strands of from about one-eighth to about 2 inches long. In articles molded from the compositions, on the other hand, even shorter lengths will be encountered because, during compounding, considerable fragmentation will occur.
The process of this invention can be carried out by a number of procedures. In one way, the difunetional epoxide compound is put into an extrusion compounder with the dry polyester and salt.
of an aliphatic carboxylic acid, and the blend is heated at an elevated temperature, .. g. , 450° - 550°F, and extruded to produce molding pellets. The difunctional epoxide compound is dispersed in the polyester resin and catalyst, and the melt viscosity is elevated in the process. In another procedure, the difunctional epoxide compound is mixed with the polyester rosin and catalyst blending at ordinary temperatures, then the blend is fluxed on a mill, heated, e.g. at 450° - 550°F, cooled and chopped. The difunctional epoxide compound can also be mixed with the powdered or granular polyester and the catalyst, and the mixture can be heated and directly formed into molded items using machines which compound and mold. In still another procedure, the difunctional epoxy compound may be incorporated in the final stage of the polyester resin manufacture process.
Compounding should be carried out to ensure that the temperature is carefully controlled; and is preferably maintained below about 530°F. Preferably the compounding is continued until an intimate blend between the resin, the catalyst and difunctional epoxide compound is obtained.
The other above-mentioned additives can be added during compounding to impart on the blend the desired characteristics, as known to those skilled in the art.

13 336-2281(8CV-5313) The compositions of the present invention may then be formed into various articles. Preferably the compounded resin is extruded into a sheet and then thermoformed into a variety of articles or is extruded into a tube. The compositions are also suitable for profile extrusion, molding and other processes known to those skilled in the art that require higher melt strength than normal systems. See, e.g. Modern Plastics Enclrclopedia '89, McGraw Hill, Vol. 65, No. 11, pp. 215 - 308.
A particularly preferred article is a core tube which covers fibers in buffer tubes and which is prepared from a polyester composition compris~d of a polyester resin, a difunctional epoxy compound and a catalyst.
DE$CRIPTIOlI O! T~ PRE!'ERRED E1180DI~NTB
The following specific examples illustrate the present invention. However, they are not to be construed to limit the claims in any manner whatsoever.
E~I~tPL~B 1-3 Polyester compositions are prepared by tumble blending the respective ingredients and compounding in a 2.5" vacuum vented Prodex single screw extruder. Tha extruder parameters were 480°F barrel sot temperature, 100 -110 rpm screw speed, and approximately 600 g/min feedrate. After drying at 120°C for four hours, the blends were injected molded into test specimens using a 480°F barrel set temperature, 140°F mold temperature, 11 second injection time, 15 second hold time, and 200 psi back pressure.
The tensile properties of the test specimens were determined on a Type V tensile bars (2.5 x 0.125 inch) using a 0.5 inch/min crosshead speed. Percent elongation was measured by crosshead displacement at break. Tensile strength is reported in psi.
The samples were further aged for hydrolysis testing. Aging was accomplished by suspending the samples in a closed container over a saturated aqueous potassium sulfate solution held at 94=

14 336-2281(8CV-5313) relative humidity and 85°C. After exposure, the samples were removed and held at ambient conditions for at least 24 hours.
Melt viscosities of the blends were measured on a Tiniua Olsen Melt Indexer. The resin blends were extruded with a 21,500 g load through a 0.0425 inch orifice at 480°F.
For comparative purposes, samples were prepared without addition of difunctional epoxide compound and catalyst.
The results along with the resin blend compositions are reported below in Table 1.

15 336-2281(8CV-5313) TABLt 1 Example A* 1 2 3 Composition Polyester', wt. % 100 99 99 98.5 Diepoxideb, wt. % -- 1 1 1.5 Catalyst', phr -- 0.025 0.05 0.05 Properties TEas molded 378 228 284 250 TS'as molded 7307 7126 6988 7058 TEaged 1 day 341 2i7 264 274 TSaged 1 day 7428 7354 7265 7340 TEaged 3 weeks 119 99 249 97.

TSaged 3 weeks 8352 7674 7560 7556 TEaged 4 weeks 93 178 223 253 TSaged 4 weeks ~ 8329 7607 7581 7287 Melt Viscosity, poise Pellets 7497 25657 28460 13783 As molded 6068 27150 28004 11940 Aged 4 weeks 686 13073 20880 9353 * = Comparative example ~hr = parts per hundred = Poly(1,4-butylene terephthalate), "VALOR" 315, General Electric Company = 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate, "BAKELITE" ERL 4221, Union Carbide Company = Sodium atearate = Tensile elongation, %
= Tensile strength, psi As is clearly demonstrated by Table 1 above, the polyester compositions having the ditunctional epoxy compound and catalyst exhibit vastly superior melt viscosity and tensile elongation properties after aging over the polyester resin alone.

20'1044 16.. 336-2Z81(8CV-5313) The procedure of Examples 1-3 is followed except the blends are compounded in a 30 mm Warner Pflaiderer twin screw extruder at a 480°F barrel set temperature, screw speed of 300 rpm and a feedrate of 250 - 320 g/min. The results, along with compositional data are set forth below in Table 2.
T
Ex- able g* C*

Composition Polyester', wt. 8 100 99 99 99 Diepoxy°, wt. ~ -_ .

Catalyst°, phr -- -- 0.05 0.1 Properties Tensile Elongation As molded Z7Z 348 261 267 Aged 1 day ZZ3 236 231 244 Aged 3 weeks 137 140 247 175 Aged 4 weeks 50 172 254 203 Aged 5 weeks 9 160 258 177 Aged 6 weeks 4 147 Z7Z 182 Melt Viscositv, poise As molded 3147 3900 7500 7161 Aged 1 day Z9a7 3366 7372 7145 Aged 3 weeks 1247 1482 6717 6315 Aged 4 weeks --- -- 6230 5839 Aged 6 weeks 133 * = Comparative Example ~hr = parts per hundred = Poly(1,4-butylene terephthalate), ~~VALOX", 5611 poise General Electric Compam = 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate, "HA1CELITE" ERL 4aZl, Union Carbide Company = Sodium stearate 20'1044 1~ 336-2Z81(8CV-5313) As can clearly be aeon from Table 2 above, the polyester composition melt blended with the difunctional epoxy compound and catalyst exhibited significantly better melt viscosity and tensile elongation retention after aging than did the polyester alone or the polyester melt blended with the difunctional epoxy compound only.
EXAIfPLZB 6-9 The procedure of Examples 1-3 is followed, except comparison is made with polyester resins blended with monofunctional epoxide compounds. The formulations are prepared so that an equivalent number of epoxide groups are introduced in each case.
The samples were aged by suspending the samples above the.
water level in a pressure steam sterilizer, Model No. 25x, Wisconsin Aluminum Foundry Company, at 1001 relative humidity, 110°C, and at a pressure of 0.4 kg/cm=. After exposure, the samples ware removed and held at ambient conditions for at least 24 hours.
The results, along with compositional data are reported below in Table 3.

207.~04~
18 336-2281(8CV-5313) Ex. ample D* E* 5 6 Composition Polyesters, wt. ; 100 100 100 100 Epoxide, phr 3.1 - b n 1.5 1 Catalyst, phr 0.06 -- 0.06 .
0.05' Properties Melt viscosity, poise 4801 5442 18531 13976 TE as molded 3a5 20Z Z64 1g8 TS as molded 6953 8078 7730 7717 TE aged 1 day 264 9Z 202 206 TS aged 1 day 7267 8070 7251 7143 TE aged 3 days 194 ZO Z20 165 TS aged 3 days 7209 8548 7327 7230 TE aged 5 days 63 4 220 185 TS aged 5 days 7486 3993 7378 7183 TE aged 7 days 17 A 156 169 TS aged 7 days 8013 A 7533 7321 * = Comparative Example ~hr = parts per hundred = Poly(1,4-butylene terephthalate), VALOR" 315, C3eneral "

Electric Company = 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate, "BAKELITE" ERL 4ZZ1, Carbide Company Union = aliphatic glycidyl ether, EPODIL" 748, Pacific Anchor "

Chemical Company = sodium stearats = potassium iodide A = too brittle to test 19 336-2Z81(8CV-5313) From Table 3 above it can clearly be seen that polyester compositions compounded with difunctional epoxy compounds have much improved melt viscosity stability over polyester compositions compounded with monofunctional epoxy compounds.
Further, it can be seen that much larger quantities of monofunctional epoxide compound are necessary to achieve some improvement in malt stability compared to the difunctional epoxy compounds. Table 3 also shows that metal halides are useful catalysts for the compositions of the present invention.
LaB 7-8 The procedure of Exa~rples 1-3 is followed except that comparison is made between the diepoxy compounds of the present invention and a trifunctional epoxide. The formulations are prepared ao that an equivalent number of epoxide groups are introduced in each case. Aging was performed employing the 110°C/1008 relative humidity exposure environment.
Results, along with compositional data are reported below in Table 4.

20 336-2281(8CV-5313) TABLE 4 . ..

Ex~ less g* G* 7 Composition Polyesteb', wt. ~ 100 100 100 100 ERL 4 Z 21 , phr -- -- 1. 3 0 . 6 4 TGIC

, phr 1.0 0.5 __ Na Stearate, phi 0.065 0.065 0.065 0 Hindered Phenol , phr 0.2 0.2 0.2 .
0.2 Properties Melt viscosity, poise As molded 26558 13725 19092 14245 Aged 3 days 1173 734 12343 2993 * = Comparative Example ~hr = parts per hundred = Poly(1,4-butylene terephthalate), "V1~I,OR" 315, General Electric Company = 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate, "BAKELITE", Union Carbide Company = Triglycidyl isocyanurate _ "IRGANO%" 1076, Ciba Geigy Company As can be clearly seen from Table 4 above, the polyester composition compounded with a difunctional epoxy compound exhibits significantly improved retention of melt viscosity after aging, than does the polyester resin treated with an equivalent number of epoxide groups from the trifunctional epoxy compound.

The procedure of Examples 1 - 3 was followed except that the amount of ERL 4221 ~aployed is varied. The results, along with compositional data, are set forth below in Table 5. A control example employing the polyester without the difunctional epoxids and catalyst is also shown.

21 336-2281(8CV-5313) 0 0 .. ~, i '~ ~ .» w o w .., a o o 'w i i n a n M o ..~~ 'e e~i n n n n n 'n o .w ~ i i 'ne r~ ~ 'gin n ~s .r o o n a ~ h n a 'e .~ 'n .r n n n n "' 'n° : , : w x n . w o n m 0 0 .r "~ n ~ n 'n a n ~ .~ n n .. ..: o o ~ ~ . n ~ a ~ h ~ h h n ., w ~ ~ a , a a s ~ x ~ x a~ a r o 0 0 , n n w n ~ n n .w ~ ", n n i ~ n '~r ~ x ~ n =

0 0 ~ n .~ n ~ a ~ a ~ .~ n a .., ~a :.x , w 0 0 0 ~ S i ~

e. n n n . ~. r .

'~ a a , , ~ x , s , a a a ~ a .. , , o .r , ,n , a a ~ ..~ ' ~
n ~
wi 'i , p ~ ~ .

~ l ~ ~ ~ ~, r = l w a ~r ~ ~ a a a s . a s as ...

~ d s ~ ~ ..
.
~a o 336-2281 (8CV-5313) Table 5 above clearly shows that polyester compositions having excellent melt viscosity properties can be obtained with a wide range of difunctional epoxy compound concentrations. Surprisingly, polyester s compositions having the highest melt. viscosity are obtained at difunctional epoxy compound concentrations of from 0.6 to 1.5 weight percent.
Many variations of the present invention will suggest themselves to those skilled in this art in light to of the above detailed description. For example, instead of poly(1, 4-butylene terephthalate), other polyester resins such as a polyethylene terephthalate), a poly(1, 4-cyclohexanedimethanol terephthalate) or mixtures thereof may be employed. Additionally, a number of other 15 difunctional expoxide compounds may be effectively employed, such as vincyclohexene di-epoxide, bis(3, 4-epoxycyclohexylmethyl)adipate, or mixture thereof. It is also within the scope of the instant invention to employ a monofunctional epoxy compound in combination with the 2o difunctional epoxy compound. Also contemplated for use herein as a catalyst compound are potassium bromide, lithium iodide, lithium fluroide, sodium acetate, potassium iodide, sodium caproate, sodium benzoate, sodium ascorbate, sodium dihydrogen phosphate, and mixtures 2s thereof. It is further contemplated to add to the polyester compositions any of the known hindered phenols, as well as a wide variety of conventional additives including, but not limited to, flame and drip retardants.
It is further within the scope of the present invention to 3o modify the compositions of the p:reseni~ invention with reinforcing agents, especially glass fibers and glass flakes. All such obvious modifications are within the full intended scope of the appended claims.

Claims (39)

1. A thermoplastic resin composition, comprising:
(a) a linear polyester resin;
(b) an effective amount of at least one difunctional epoxy compound, said at least one difunctional epoxy compound having at least one cyclohexane ring moiety and having two terminal epoxy functional groups, wherein at least one of the two terminal epoxy functional groups is a substituent on the at least one cyclohexane ring moiety; and (c) an effective amount of a catalyst compound;
wherein the amounts of components (b) and (c) are effective to provide improved melt viscosity stability.

2. A composition as defined in claim 1 wherein said component (a) polyester resin comprises units of an aliphatic diol, a cycloaliphatic diol or a mixture of such diols and an aromatic diacid.

3. A composition as defined in claim 2 wherein said component (a) is selected from the group consisting of a poly(1,4-butylene terephthalate), poly(ethylene terephthalate), poly(1,4-cyclohexanedimethanol terephthalate) and blends of any of the foregoing.

4. A composition as defined in claim 3 wherein said component (a) comprises poly(1,4-butylene terephthalate) .

5. A composition as defined in claim 1 wherein said component (a) polyester resin has an intrinsic viscosity of at least about 0.4 deciliters per gram when measured in a 60:40 mixture of phenol and trichloroethane at 25°C.

6. A composition as defined in claim 1 wherein said at least one difunctional epoxy compound is selected from the group consisting of bis(3,4-epoxycyclohexylmethyl) adipate;
vinylcyclohexene diepoxide; 3,4-epoxycyclohexl-3,4-epoxycyclohexcarboxylate; 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexlcarboxylate and mixtures of any of the foregoing.

7. A composition as defined in claim 6 wherein said difunctional epoxy compound comprises 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexlcarboxylate.

8. A composition as defined in claim 1 wherein said catalyst compound (c) comprises a salt free from direct carbon-phosphorous bonds and containing at least one of alkali metal cations and alkaline earth metal cations and halide anions.

9. A composition as defined in claim 8 wherein said catalyst compound (c) is selected from the group consisting of potassium bromide, potassium iodide, lithium iodide, lithium fluoride, sodium acetate, sodium caproate, sodium benzoate, sodium stearate, sodium ascorbate, sodium dihydrogen phosphate, dodecyltrimethylammonium bromide and mixtures thereof.

10. A composition as defined in claim 9 wherein said catalyst component comprises sodium stearate.

11. A composition as defined in claim 1 wherein said composition further comprises:
(d) a hindered phenol antioxidant.

12. A composition as defined in claim 1 wherein said composition further comprises an additive selected from the group consisting of flame retardants, drip retardants, reinforcers, dyes, pigments, stabilizers, nucleants, rubbery impact modifiers and mixtures of any of the foregoing.

13. A composition as defined in claim 1 wherein said difunctional epoxy compound is present in an amount ranging from about 0.1 to about 3.5 weight percent based on the total weight of the composition.

14. A composition as defined in claim 13 wherein said difunctional epoxy compound is present in an amount ranging fro~n about 0.5 to about 2 weight percent based on the total weight of the composition.

15. A composition as defined in claim 14 wherein said difunctional epoxy compound is present in an amount ranging from about 1 to about 1.5 weight percent based on the total weight of the composition.

16. A composition as defined in claim 1 wherein said catalyst compound is present in an amount ranging from about 0.01 to about 1 weight percent based on the total weight of the composition.

17. A composition as defined in claim 16 wherein said catalyst compound is present in an amount ranging from about 0.03 to about 0.1 weight percent based on the total weight of the composition.

18. A method for improving the hydrolytic stability of a thermoplastic linear polyester composition comprising compounding:
(a) a linear polyester resin;
(b) from 0.1 percent by weight to 5 percent by weight of at least one difunctional epoxy compound, said at least one difunctional epoxy compound having at least one cyclohexane ring moiety and having two terminal epoxy functional groups, wherein at least one of the two terminal epoxy functional groups is a substituent on the at least one cyclohexane ring moiety and wherein the amount of difunctional epoxy compound is based on the combined weights of the linear polyester resin and difunctional epoxy compound; and (c) from 0.01 percent by weight to 1 percent by weight of a catalyst, wherein the amount of catalyst is based on the total weight of the resin composition.

19. A method as defined in claim 18 wherein said polyester resin comprises units of an aliphatic diol, a cycloaliphatic diol or a mixture of such diols and an aromatic diacid.

20. A method as defined in claim 17 wherein said polyester resin is selected from the group consisting of poly(1,4-butylene terephthalate), a poly(1,4-cyclohexanedimethanol terephthalate), a poly)ethylene terephthalate), and blends of any of the foregoing.

21. A method as defined in claim 20 wherein said polyester resin comprises a poly (1,4-butylene terephthalate).

22. A method as defined in claim 18 wherein said polyester resin has an intrinsic viscosity of at least about 0.4 deciliters per gram when measured in a 60:40 mixture of phenol and trichloroethane at 25°C.

23. A method as defined in claim 18 wherein said at least one difunctional epoxy compound is selected from the group consisting of bis(3,4-epoxycyclohexylmethyl) adipate;
vinylcyclohexene diepoxide; 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexlcarboxylate; 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexlcarboxylate and mixtures of any of the foregoing.

24. A method as defined in claim 23 wherein said difunctional epoxy compound comprises 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate.

25. A method as defined in claim 18 wherein said catalyst compound comprises salts free from direct carbon-phosphorous bonds and containing at least one of alkali metal cations and alkaline earth metal cations and halide ions.

26. A method as defined in claim 25 wherein said catalyst compound is selected from the group consisting of potassium bromide, potassium iodide, lithium iodide, lithium fluoride, sodium acetate, sodium caproate, sodium benzoate, sodium stearate, sodium ascorbate, sodium dihydrogen phosphate, dodecyltrimethylammonium bromide and mixtures thereof .

27. A method as defined in claim 26 wherein said catalyst compound comprises sodium stearate.

28. A method as defined in claim 18 wherein said method further comprises compounding into the composition a hindered phenol antioxidant.

29. A method as defined in claim 18 wherein said method further comprises compounding into the composition an additive selected from the group consisting of flame retardants, drip retardants, dyes, pigments, stabilizers, plasticizers, nucleants, reinforcers, rubbery impact modifiers and mixtures of any of the foregoing.

30. A method as defined in claim 18 wherein said compounding comprises melt blending or milling.

31. A method as defined in claim 18 wherein said effective amount of a difunctional epoxy compound comprises from about 0.1 to about 3.5 weight percent based on the total weight of the compounded composition.

32. A method as defined in claim 31 wherein said effective amount of a difunctional epoxy compound comprises from about 0.5 to about 2 weight percent based on the total weight of the compounded composition.

33. A method as defined is claim 32 wherein said effective amount of a difunctional epoxy compound comprises from about 1 to about 1.5 weight percent based on the total weight of the compounded composition.

34. A method as defined in claim 33 wherein said effective amount of a catalyst compound comprises from about 0.01 to about 1 weight percent based on the total weight of the compounded composition.

35. A method as defined in claim 34 wherein said effective amount of a catalyst compound comprises from about 0.03 to about 0.1 weight percent based on the total weight of the compounded composition.

36. A method for making an article, comprising:
extruding and thermoforming, extruding or molding the composition as defined in claim 1.

37. An article made by the process of claim 36.

38. An article according to claim 37, wherein the article comprises a tube.

39. The reaction product of claim 18.