Blend of Polyarylene Sulfide and Wholly Aromatic Polyester

The present invention relates to a blend of polyarylene sulfide and melt processable wholly aromatic polyester. The characteristics and properties of such a blend differ significantly from those expected in light of observations of the properties of ordinary mixtures and of most polymeric blends.

When a blend or mixture is prepared from two or more ordinary, non-polymeric materials, a random distribution of the molecules of the components is obtained. This random distribution provides complete mixing without the formation of groups or clusters of the molecules of any one component. Such a mixture is expected to follow the "Rule of Mixtures." The Rule of Mixtures predicts the numerical values of properties of a blend to be the weighted average of the numerical values of the properties of the components.

A discussion of the Rule of Mixtures can be found in Predicting the Properties of Mixtures: Mixture Rules in Science and Engineering, by Lawrence E. Nielsen, Marcel Dekker Inc. (New York).

Further information with regard to the Rule of Mixtures can be found on pages 395, 436, 465, 492, and 500 of Volume 2 of Mechanical Properties of Polymers and Composites, by Lawrence E. Neilsen, Marcel Dekker Inc. (New York: 1974). As stated therein, mixtures of a polymer matrix with a fibrous reinforcing agent, a ribbon-shaped filler, or a rod-shaped filler are known to follow the Rule of Mixtures. The above-cited reference further discloses that mixtures of phase inverted isotropic interpenetrating polymer networks, such as a phase inverted network of polystyrene and polybutadiene, are also known to follow the Rule of Mixtures.

Mixtures of most chemically distinct polymeric materials have been found to deviate from the behavior of ordinary mixtures as characterized by the Rule of Mixtures. The sheer size of polymeric chains restricts mixing of the components and leads to the formation of domains or clusters of molecules of the individual components. Thus, it can be said that most chemically distinct polymeric materials tend to be incompatible in mixtures, exhibiting a tendency to separate into phases. There exists a boundary between the domains of the component polymers, and articles made from such a blend would be expected to exhibit failure at the boundary when placed under stress. In general, then, the mechanical properties of the product are commonly reduced rather than enhanced. Specific properties which may be thus affected include tensile strength, tensile modulus, flexural strength, flexural modulus, and impact strength.

Some polymeric materials, such as polyarylene sulfide and most wholly aromatic polyesters, exhibit an ordered structure in at least some regions of the polymer. This order can exist in one, two, or three dimensions. The inclusion in blends of polymeric materials exhibiting an ordered structure leads to an increased tendency of the blends to separate into phases. This is due to the fact that the order found in certain regions of the polymer causes a fairly sharp boundary between the domains of the molecules of the component polymers. Thus, blends including such polymers would be expected to exhibit a significant reduction in mechanical properties. Accordingly, there has been little impetus to form such blends, particularly for use in applications where mechanical properties are of importance.

U.K. Published Patent Application No. 2,008,598 discloses a polymer composition comprising 20 percent or less, based upon the total weight of polymeric material, of a first rigid polymeric material with the balance being a second polymeric material composed substantially of flexible moleclar chains. An approximal borderline between rigid and flexible molecular chains is a Mark-Houwink Index of 1, those above being rigid and those below being flexible. The first polymeric material is dispersed in the second polymeric material in a microscopic region of 1 .mu.m. or less. Foreign counterparts of this application include Japan No. 54065747, French No. 2407956, and West German No. 2847782. Although no published value of the Mark-Houwink Index of a polyarylene sulfide is known to applicant, it is believed that polyarylene sulfides would be characterized by those of ordinary skill in the art as rigid molecules within the context of the above-cited application. The application does not disclose blends of two or more polymeric materials having rigid molecular chains.

It is therefore an object of the present invention to provide a blend of polyarylene sulfide and wholly aromatic polyester which exhibits satisfactory mechanical properties, such as tensile strength, tensile modulus, flexural strength, flexural modulus, impact strength, and heat deflection temperature

It is also an object of the present invention to provide a blend of polyarylene sulfide and wholly aromatic polyester which exhibits improved melt processability.

It is also an object of the present invention to provide a blend of polyarylene sulfide and wholly aromatic polyester which exhibits no significant reduction in mechanical properties, such as tensile and flexural properties, as compared to the weighted average of the mechanical properties of the individual components.

It is also an object of the present invention to provide a blend of polyarylene sulfide and wholly aromatic polyester which exhibits a high degree of anisotropy and shear sensitivity in the melt.

It is also an object of the present invention to provide a blend of polyarylene sulfide and wholly aromatic polyester which, by virtue of the inclusion of a relatively less expensive component, is less expensive than the relatively more expensive component alone and which exhibits no significant reduction in mechanical properties.

These and other objects as well as the scope, nature, and utilization of the present invention will be apparent from the following description and appended claims.

The present invention provides a polymer blend which is capable of exhibiting an anisotropic melt phase, improved processability characteristics, and the ability to form molded articles having satisfactory mechanical properties. The blend comprises:

(a) approximately 5 to approximately 95 percent by weight, based upon the total weight of components (a) and (b), of a polyarylene sulfide, and

(b) approximately 5 to approximately 95 percent by weight, based upon the total weight of components (a) and (b), of a melt processable wholly aromatic polyester which is capable of forming an anisotropic melt phase apart from the blend.

Blend compositions containing high concentrations of wholly aromatic polyester (i.e., at least 60 percent by weight wholly aromatic polyester) can be used to form fibers and films.

The present invention provides a blend of polyarylene sulfide and melt processable, wholly aromatic polyester. As used herein, the term "blend" includes any physical blend, mixture, or alloy of the above polymeric components.

The first component of the blend provided by the present invention is a polyarylene sulfide. Polyarylene sulfide polymers may be formed by the reaction of at least one polyhalo-substituted cyclic compound with an alkali metal sulfide in a reaction medium comprising a polar organic compound, as disclosed in U.S. Pat. No. 3,354,129, which is herein incorporated by reference.

Some specific examples of polyarylene sulfides are the reaction products of the reaction of alkali metal sulfides, such as the monosulfides of sodium, potassium, lithium, rubidium, and cesium, with the following polyhalo-substituted compounds:

1,2-dichlorobenzene

1,3-dichlorobenzene

1,4-dichlorobenzene

2,5-dichlorobenzene

1,4-dibromobenzene

1,4-diiodobenzene

1,4-difluorobenzene

2,5-dibromoaniline

N,N-dimethyl-2,5-dibromoaniline

1,3,5-trichlorobenzene

1,2,4,5-tetrabromobenzene

hexachlorobenzene

1-n-butyl-2,5-dichlorobenzene

1-cyclohexyl-2,5-diiodobenzene

1-isooctyl-2,4-difluorobenzene

1-n-dodecyl-2,5-dichlorobenzene

1-benzyl-2,5-dibromobenzene

1,4-di-n-butyl-2,5-dichlorobenzene

1,4-di-n-nonyl-2,6-di-bromobenzene

1,3,5-trichloro-2,4,6-triphenylbenzene

1,4-dibromo-2,3,5,6-tetra(4-ethylphenyl)benzene

methyl 2,5-dichlorobenzoate

isopropyl 2,3,5-tribromobenzoate

cyclohexyl 2,4,6-triiodobenzoate

phenyl 2,3,4,5,6-pentachlorobenzoate

2,5-dichlorobenzamide

N,N-di-n-dodecyl-2,4,5-tribromobenzamide

ethyl 2,4,5-trichloroacetanilide

cyclohexyl N-methyl-2,5-dibromoacetanilide

1,4-dibromonaphthalene

1,4-dichloro-7,8-diethylnaphthalene

1-methoxy-2,5-dichlorobenzene

1-cyclohexylthio-2,5-dichlorobenzene

1,4,7,8-tetrabromo-2,3,5,6-tetra-n-butylnaphthalene

1,3,5-trichloro-7-aminonaphthalene

n-octyl 2,4-dibromo-naphthalene-1-carboxylate

N,N-dimethyl-5,6,7,8-tetrabromo-1-naphthalene carboxamide

1-acetamido-2,4-dibromonaphthalene

8-decoxy-1,4-difluoronaphthalene

6,7-dibenzyl-8-methylthio-1,4-dichloroaphthalene

1,4-dichloroanthracene

1,7-dibromo-6-cyclohexylanthracene

2,8-diiodo-3,7-diethylanthracene

1-dodecyl-2,6-difluoroanthracene

1,2,4-trichloro-6-carbethoxyanthracene

2,6-dibromo-8-amiaoanthracene

3,7-diiodo-4-cyclohexylthioanthracene

n-decyl 3,8-difluoroanthracene carboxylate

1-acetamido-2,4-dibromoanthracene

10-dodecoxy-1,3,5-trichloroanthracene

4,4'-dichlorobiphenyl

3,4'-dibromo-2-aminobiphenyl

2,2',4-tribromo-6-acetamidobiphenyl

3,3'-dichloro-4,4'-didodecylbiphenyl

4,4'-diiodo-3-ethoxy-6-n-octylbiphenyl

2,2',4,4'-tetrabromo-6-N,N-dimethylaminobiphenyl

4,4'-dichloro-3,3'-dicylohexylbiphenyl

4,4"-dibromo-p-terphenyl

3,3',3"-trichloro-p-terphenyl

4,4"-dichloro-3'-acetamido-p-terphenyl

4,4"-difluoro-2,2',2"-tri-n-decyl-3'-methoxy-p-terphenyl

4,4"-dibromo-3'-carbbutoxy-p-terphenyl

4,4"-dichloro-2-(N-acetylamino)-p-terphenyl

3,4-dibromothiophene

3,4-dichlorofuran

3,4-difluoropyrrole

2,5-dibromo-4-aminothiophene

2,5-dichloro-3-ethoxythiophene

3,4-difluoro-5-acetamidofuran

3,4-dibromo-5-carbethoxypyrrole

2,5-dichloropyridine

3,5-dibromo-4-methylpyridine

4,8-diodoquinoline

2,3,6,7-tetrachloro-4,5-di-n-butylquinoline

1,4-dibromo-2,3,5,6-tetrafluorobenzene

4-chlorobromobenzene

2,5-dichlorobenzenesulfonic acid

sodium 2,5-dibromobenzenesulfonate

2,8-difluoronaphthalenecarboxylic acid

lithium 2,7-diiodoanthracenecarboxylate

p,p'-dichlorodiphenyl ether

o,p'-dibromodiphenylamine

2,4'-difluorodiphenylmethane

3,3'-dichlorodiphenyl dimethylsilane

di(2-methyl-4-bromophenyl) sulfoxide

methyl di(3-ethyl-4-chlorophenyl) phosphite

4-bromophenyl 3-n-butyl-4-chlorophenyl sulfone

2,6-dichloropyrazine

The polyarylene sulfide which is preferred for use in the blend of the present invention is polyphenylene sulfide, which has the following structure: ##STR1## This polymer is available commercially from Phillips Petroleum Company under the trademark Ryton.RTM.. The polymer exhibits a high degree of crystallinity, good chemical resistance, and good thermal stability. The polymer is characterized by high stiffness and good retention of mechanical properties at high temperatures. At normal temperatures, the unfilled polymer is a hard material with relatively high tensile and flexural strengths. Substantial increases in these properties are realized by the addition of fillers, especially glass. There are no known solvents below approximately 200.degree. C.

Polyphenylene sulfide exhibits certain disadvantages. The polymer exhibits relatively poor melt processability characteristics and is generally difficult to mold in the absence of a filler, such as glass. However, articles molded from glass-filled polyphenylene sulfide commonly exhibit poor surface characteristics. Moreover, the polymer does not possess sufficient melt strength to support a molten strand of the polymer (e.g., an extruded strand), and special equipment is therefore necessary to handle extruded polyphenylene sulfide.

The wholly aromatic polyesters which may be used as a component in the blend of the present invention comprise at least two recurring moieties which, when combined in the polyester, have been found to form an atypical anisotropic melt phase. The aromatic polyesters are considered to be "wholly" aromatic in the sense that each moiety present in the polyester contributes at least one aromatic ring to the polymer backbone.

Wholly aromatic polyester resins long have been known. For instance, 4-hydroxybenzoic acid homopolymer and copolymers have been provided in the past and are commercially available. Certain of the wholly aromatic polyesters encountered in the prior art tend to be somewhat intractable in nature and to present substantial difficulties if one attempts to melt process the same while employing conventional melt processing procedures. Such polymers commonly are crystalline in nature, relatively high melting or possess a decomposition temperature which is below the melting point, and when molten frequently exhibit an isotropic melt phase. Molding techniques such as compression molding or sintering may be utilized with such materials; however, injection molding, melt spinning, etc., commonly have not been viable alternatives or when attempted commonly have been accomplished with difficulty. It is to be understood that the wholly aromatic polyesters which are suitable for use in the present invention are limited to those which are capable of undergoing melt processing, i.e., those which exhibit no substantial decomposition at or below the melting temperature.

In addition to being wholly aromatic and capable of undergoing melt processing, the polyesters which are useful as a component in the blend of the present invention must exhibit, apart from the blend, optical anisotropy in the melt. Recent publications disclosing such polyesters include (a) Belgian Pat. Nos. 828,935 and 828,936, (b) Dutch Pat. No. 7505551, (c) West German Pat. Nos. 2,520,819, 2,520,820, and 2,722,120, (d) Japanese Pat. Nos. 43-223, 2132-116, 3017-692, and 3021-293, (e) U.S. Pat. Nos. 3,991,013; 3,991,014; 4,057,597; 4,066,620; 4,075,262; 4,118,372; 4,156,070; 4,159,365; 4,169,933; and 4,181,792; and (f) U.K. Application No. 2,002,404.

Wholly aromatic polyesters which are preferred for use in the present invention are disclosed in commonly-assigned U.S. Pat. Nos. 4,067,852; 4,083,829; 4,130,545; 4,161,470; and 4,184,996; and in commonly-assigned U.S. Application Ser. Nos. 10,392, filed Feb. 8, 1979 (now U.S. Pat. No. 4,238,599); 10,393, filed February 8, 1979 (now U.S. Pat. No. 4,238,598); 17,007, filed Mar. 2, 1979; 21,050, filed Mar. 16, 1979 (now U.S. Pat. No. 4,224,433); 32,086, filed Apr. 23, 1979 (now U.S. Pat. No. 4,219,461); and 54,049, filed July 2, 1979. The disclosures of all of the above-identified commonly-assigned U.S. Patents and Applications are herein incorporated by reference. The wholly aromatic polyesters disclosed therein typically are capable of forming an anisotropic melt phase apart from the blend at a temperature below approximately 350.degree. C.

The wholly aromatic polyesters which are suitable for use in the blend of the present invention may be formed by a variety of ester-forming techniques whereby organic monomer compounds possessing functional groups which upon condensation form the requisite recurring moieties are reacted. For instance, the functional groups of the organic monomer compounds may be carboxylic acid groups, hydroxyl groups, ester groups, acyloxy groups, acid halides, etc. The organic monomer compounds may be reacted in the absence of a heat exchange fluid via a melt acidolysis procedure. They, accordingly, may be heated initially to form a melt solution of the reactants with the reaction continuing as solid polymer particles are suspended therein. A vacuum may be applied to facilitate removal of volatiles formed during the final stage of the condensation (e.g., acetic acid or water).

In commonly-assigned U.S. Pat. No. 4,083,829, entitled "Melt Processable Thermotropic Wholly Aromatic Polyester," is described a slurry polymerization process which may be employed to form the wholly aromatic polyesters which are suitable for use in the present invention. According to such a process, the solid product is suspended in a heat exchange medium. The disclosure of this patent has previously been incorporated herein by reference.

When employing either the melt acidolysis procedure or the slurry procedure of U.S. Pat. No. 4,083,829, the organic monomer reactants from which the wholly aromatic polyesters are derived may be initially provided in a modified form whereby the usual hydroxy groups of such monomers are esterified (i.e., they are provided as lower acyl esters). The lower acyl groups preferably have from about two to about four carbon atoms. Preferably, the acetate esters of organic monomer reactants are provided.

Representative catalysts which optionally may be employed in either the melt acidolysis procedure or in the slurry procedure of U.S. Pat. No. 4,083,829 include dialkyl tin oxide (e.g., dibutyl tin oxide), diaryl tin oxide, titanium dioxide, antimony trioxide, alkoxy titanium silicates, titanium alkoxides, alkali and alkaline earth metal salts of carboxylic acids (e.g., zinc acetate), the gaseous acid catalysts, such as Lewis acids (e.g., BF.sub.3), hydrogen halides (e.g., HCl), etc. The quantity of catalyst utilized typically is about 0.001 to 1 percent by weight based upon the total monomer weight, and most commonly about 0.01 to 0.2 percent by weight.

The wholly aromatic polyesters suitable for use in the present invention tend to be substantially insoluble in common polyester solvents and accordingly are not susceptible to solution processing. As discussed previously, they can be readily processed by common melt processing techniques. Most suitable wholly aromatic polyesters are soluble in pentafluorophenol.

The wholly aromatic polyesters which are suitable for use in the blend of the present invention commonly exhibit a weight average molecular weight of about 2,000 to 200,000, and preferably about 10,000 to 50,000, e.g., about 20,000 to 25,000. Such molecular weight may be determined by standard techniques not involving the solutioning of the polymer, e.g., by end group determination via infrared spectroscopy on compression molded films. Alternatively, light scattering techniques in a pentafluorophenol solution may be employed to determine the molecular weight.

The wholly aromatic polyesters additionally commonly exhibit an inherent viscosity (i.e., I.V.) of at least approximately 2.0 dl./g., e.g., approximately 2.0 to 8.0 dl./g., when dissolved in a concentration of 0.1 percent by weight in pentafluorophenol at 60.degree. C.

The liquid crystalline, wholly aromatic polyesters appear to have excellent electrical properties when used as films or coatings in electrical applications. They have high temperature resistance and high dielectric strength, i.e., they are capable of withstanding high voltages without exhibiting substantial breakdown.

The above-described polyesters, in order to be useful in the blend of the present invention, must exhibit optical anisotropy in the melt phase. These polyesters readily form liquid crystals in the melt phase and accordingly exhibit a high tendency for the polymer chains to orient in the shear direction. Such anisotropic properties are manifested at a temperature at which the wholly aromatic polyester readily undergoes melt processing to form shaped articles. The anisotropic properties may be confirmed by conventional polarized light techniques whereby crossed-polarizers are utilized. More specifically, the anisotropic melt phase may conveniently be confirmed by the use of a Leitz polarizing microscope at a magnification of 40X with the sample on a Koffler hot stage and under a nitrogen atmosphere. The melt phases of the wholly aromatic polyesters which are suitable for use in the present invention are optically anisotropic, i.e., they transmit light when examined between crossed-polarizers. By contrast, the melt of a conventional polymer will not transmit appreciable light when placed between crossed-polarizers.

The wholly aromatic polyesters described above are useful as molding resins and may also be used in the formation of coatings, fibers, and films. They may be molded by injection molding and can be processed by any melt extrusion technique.

Especially preferred wholly aromatic polyesters are those which are disclosed in U.S. Pat. No. 4,184,996 and U.S. Application Ser. No. 10,392, filed Feb. 8, 1979 (now U.S. Pat. No. 4,238,599).

The polyester disclosed in U.S. Pat. No. 4,184,996 is a melt processable wholly aromatic polyester which is capable of forming an anisotropic melt phase at a temperature below approximately 325.degree. C. apart from the blend. The polyester consists essentially of the recurring moieties I, II, and III wherein: ##STR2## The polyester comprises approximately 30 to 70 mole percent of moiety I. The polyester preferably comprises approximately 40 to 60 mole percent of moiety I, approximately 20 to 30 mole percent of moiety II, and approximately 20 to 30 mole percent of moiety III.

The polyester disclosed in U.S. Application Ser. No. 10,392 is a melt processable wholly aromatic polyester which is capable of forming an anisotropic melt phase, apart from the blend, at a temperature no higher than approximately 320.degree. C. The polymer consists essentially of the recurring moieties I, II, III, and IV wherein: ##STR3## where R is methyl, chloro, bromo, or mixtures thereof, and is substituted for a hydrogen atom present upon the aromatic ring. The R group is preferably a methyl group.

The polyester comprises approximately 20 to 60 mole percent of moiety I, approximately 5 to 18 mole percent of moiety II, approximately 5 to 35 mole percent of moiety III, and approximately 20 to 40 mole percent of moiety IV. The polyester preferably comprises approximately 35 to 45 mole percent of moiety I, approximately 10 to 15 mole percent of moiety II, approximately 15 to 25 mole percent of moiety III, and approximately 25 to 35 mole percent of moiety IV, with the proviso that the total molar concentration of moieties II and III is substantially identical to that of moiety IV.

The wholly aromatic polyester described immediately above is most preferred for inclusion in the blend of the present invention. This wholly aromatic polyester commonly exhibits an inherent viscosity of at least 2.0 dl./g., e.g., 2.0 to 8.0 dl./g., when dissolved in a concentration of 0.3 weight/volume percent in pentafluorophenol at 60.degree. C.

For the purposes of the present invention, the aromatic rings which are included in the polymer backbones of the polymer components may include substitution of at least some of the hydrogen atoms present upon an aromatic ring. Such substituents include alkyl groups of up to five carbon atoms; alkoxy groups having up to five carbon atoms; halogens; and additional aromatic rings, such as phenol and substituted phenol groups. Halogens which may be listed as possible substituents include fluorine, chlorine, and bromine. Although bromine atoms tend to be released from organic compounds at high temperatures, bromine is more stable on aromatic rings than on aliphatic chains, and therefore is suitable for inclusion as a possible substituent on the aromatic rings in the present blend.

The blend of the present invention comprises approximately 5 to approximately 95 percent by weight of the polyarylene sulfide component and approximately 5 to approximately 95 percent by weight of the wholly aromatic polyester component. Preferably, the blend comprises approximately 5 to approximately 75 percent by weight of the polyarylene sulfide component and approximately 25 to approximately 95 percent by weight of the wholly aromatic polyester component. More preferably, the blend comprises approximately 5 to approximately 40 percent by weight of the polyarylene sulfide component and approximately 60 to approximately 95 percent by weight of the wholly aromatic polyester component. The above weight percentages are based upon the total weight of the wholly aromatic polyester component and the polyarylene sulfide component.

In preparing the blend of the present invention, the individual components are commonly provided in the form of chips or pellets. Each of the components is weighed separately, and then the components are physically mixed together in any appropriate apparatus, e.g., a ball mill. The physical mixture is then dried at approximately 100.degree. C. overnight or for a period of time of approximately 24 hours. The mixture is conveniently dried in a vacuum oven or in a circulating air oven, although any suitable apparatus may be used. The purpose of the drying step is to remove water from the physical mixture so as to prevent degradation of the polymer blend. After the mixture of solid polymer particles has been dried, the polymer blend can then be prepared. A convenient method of forming the polymer blend is melt extrusion. The extrusion apparatus thoroughly mixes the polymers in the melt and then extrudes the blend in the form of a strand which, upon solidification, can be broken up into chips or pellets.

As previously discussed, it is known in the art that blends of two polymers tend to exhibit phase separation, with a concomitant reduction in properties, due to the incompatibility of the polymers, i.e., the formation of domains. However, unexpected and surprising results are achieved with the blend of the present invention. It has been observed that there is no significant reduction in mechanical properties, such as tensile and flexural properties, of the blend when compared to the weighted average of the mechanical properties of the components. Moreover, the blend of the present invention also provides an economic advantage. The combination of the relatively less expensive polyarylene sulfide with the relatively more expensive wholly aromatic polyester produces a blend which costs less than the more expensive component but which exhibits no significant decrease in mechanical properties.

In addition, the blend of the present invention exhibits improved processability over the polyarylene sulfide alone. For example, as discussed above, polyphenylene sulfide is difficult to mold in the absence of a filler, but a blend of wholly aromatic polyester and polyphenylene sulfide can be molded without the need for fillers. Moreover, the blend possesses sufficient melt strength to be melt processed without requiring special equipment, as is required by polyphenylene sulfide alone.

The blend of the present invention is capable of undergoing melt processing at a temperature within the range of approximately 260.degree. C. to 350.degree. C. Preferably, the blend is capable of undergoing melt processing at a temperature within the range of approximately 280.degree. C. to 300.degree. C.

The blend of the present invention demonstrates anisotropy in the melt phase. This is due to the fact that the wholly aromatic polyester has been found to retain its anisotropic characteristics in spite of the presence of the other component. Thus, the blend retains the excellent processability characteristics of the liquid crystalline polymer.

The blend of the present invention is useful as a molding and extrusion resin, and especially for injection molding. Blend compositions containing high concentrations of wholly aromatic polyester (i.e., at least 60 percent by weight of wholly aromatic polyester) can be used in the formation of fibers and films. Articles molded from the blend of the present invention exhibit satisfactory mechanical properties, such as tensile strength, tensile modulus, flexural strength, flexural modulus, notched Izod impact strength, and heat deflection temperature.

Articles may also be molded from a molding compound which includes, as one component, the blend of the present invention. Such a molding compound incorporates into the blend of the present invention approximately 1 to 50 percent, preferably approximately 10 to 30 percent, by weight, based upon the total weight of the molding compound, of a solid filler and/or reinforcing agent. Representative fibers which may serve as reinforcing media include glass fibers, asbestos, graphitic carbon fibers, amorphous carbon fibers, synthetic polymeric fibers, aluminum fibers, aluminum silicate fibers, oxide of aluminum fibers, titanium fibers, magnesium fibers, rock wool fibers, steel fibers, tungsten fibers, cotton, wool, and wood cellulose fibers, etc. Representative filler materials include calcium silicate silica, clays, talc, mica, polytetrafluoroethylene, graphite, alumina trihydrate, sodium aluminum carbonate, barium ferrite, etc.

In order to form an article by injection molding from the present blend, or from a molding compound made from the present blend, the blend or molding compound is brought to the melt temperature of the blend, e.g., approximately 280.degree. C. to 300.degree. C., and is then injected into a mold cavity. The mold cavity is commonly maintained at a temperature less than approximately 100.degree. C., e.g., approximately 90.degree. C. to 100.degree. C. The blend in its melt phase is injected into the mold cavity at a pressure of approximately 10,000 p.s.i. The cycle time (i.e., the time between injections) for the present blend commonly is about 10 to 40 seconds.

It has been observed that the properties of articles formed from the blend of the present invention vary with the processing conditions, such as mold temperature, injection pressure, cycle time, etc. However, it would be obvious to one of ordinary skill in the art to experimentally determine those conditions which maximize the properties of articles formed from the present blend.

The following examples are given as specific illustrations of the invention. It should be understood, however, that the invention is not limited to the specific details set forth in the examples.

Blend compositions were prepared by the melt extrusion of polyphenylene sulfide and a wholly aromatic polyester comprising 40 mole percent of 4-oxybenzoyl units, 15 mole percent of 1,2-ethylenedioxy-4,4'-dibenzoyl units, 15 mole percent of terephthaloly units, and 30 mole percent of methyl substituted 1,4-dioxyphenylene units. The wholly aromatic polyester exhibited an inherent viscosity (I.V.) of 2.34 dl./g. when dissolved in a concentration of 0.3 weight/volume percent in pentafluorophenol at 60.degree. C. The polyphenylene sulfide used was P-6 injection molding grade Ryton.RTM. polyphenylene sulfide obtained commercially from Phillips Petroleum Company. The ratios of wholly aromatic polyester:polyphenylene sulfide in the blend compositions were 90:10, 60:40, 30:70, and 10:90.

The component polymers, in the form of solid particles, such as chips or pellets, were weighed separately and were subsequently physically mixed together in a ball mill. The mixture of solid particles was dried at approximately 100.degree. C. overnight in a vacuum oven or circulating air oven. The mixture of solid particles was then heated until a melt phase was formed, and the melt was thoroughly mixed in a conventional melt extrusion apparatus. The resulting blend was extruded into the form of a strand, which, upon solidification, was broken up into solid particles of the polymer blend.

In order to measure the mechanical properties of the blend, shaped articles were molded from the polymer blends. The solid particles of the various compositions were heated to the melt temperature of the blend (approximately 280.degree. C.), and were subsequently injected into a mold cavity at an injection pressure of approximately 10,000 p.s.i. The mold cavity was held at a temperature of approximately 94.degree. C. The cycle time for the injection molding process was approximately 40 seconds.

The mechanical properties of the blend were measured and are shown in Table I.

The tensile properties were determined in accordance with standard test ASTM D638, Type V; the flexural properties were determined in accordance with ASTM D790; the notched Izod impact strength was determined in accordance with ASTM D256; and the heat deflection temperature was determined in accordance with ASTM D648.

The data for tensile strength and flexural strength demonstrate the surprising and unexpected results provided by the blend compositions prepared in accordance with this Example. In general, there is no significant reduction in the tensile and flexural properties as compared to the weighted average of the properties of the individual components. It can be seen that articles formed from compositions containing at least 60 percent wholly aromatic polyester exhibit tensile and flexural strengths of no less than approximately 19,000 p.s.i.

Articles were molded in the manner described in Example 1 from blend compositions prepared from polyphenylene sulfide and a second batch of the wholly aromatic polyester used in Example 1. The wholly aromatic polyester exhibited an inherent viscosity of 2.47 when dissolved in a concentration of 0.3 weight/volume percent in pentafluorophenol at 60.degree. C. The mechanical properties of the articles were measured according to the tests listed in Example 1, and the results are given in Table II.

The data indicate that, contrary to expectations, there is no significant reduction in most properties, as compared to the weighted average of the properties of the individual components. Articles formed from the blend compositions of the present Example, which contain at least 60 percent wholly aromatic polyester, exhibit tensile and flexural strengths of no less than approximately 19,000 p.s.i.

Blend compositions were prepared in the manner described in Example 1 from polyphenylene sulfide and a wholly aromatic polyester comprising 60 mole percent of 4-oxybenzoyl units, 20 mole percent of 2,6-dioxynaphthalene units, and 20 mole percent of terephthaloyl units. The wholly aromatic polyester exhibited an I.V. of 2.9 dl./g. when dissolved in a concentration of 0.1 percent by weight in pentafluorophenol at 60.degree. C. The ratios of wholly aromatic polyester:polyphenylene sulfide of the blend compositions were 90:10, 80:20, 70:30, 50:50, 30:70, and 10:90.

Articles were molded from the blend compositions of the present Example in the manner described in Example 1. The mechanical properties of these articles were measured according to the tests listed in Example 1. The results of these tests are listed in Table III.

As the data indicate, there is no significant reduction in most properties, as compared to the weighted average of the properties of the individual components. On the contrary, the addition of polyphenylene sulfide to the wholly aromatic polyester provides a blend which is less expensive than the wholly aromatic polyester alone, yet which retains satisfactory mechanical properties.

It is to be understood that the foregoing detailed description is given merely by way of illustration and that many variations may be made therein without departing from the spirit of the invention.