Thermoplastic elastomers based upon chlorinated polyethylene and a crystalline olefin polymer

BACKGROUND OF THE INVENTION
The present invention generally concerns thermoplastic elastomer compositions comprising blends of chlorinated polyethylene and a crystalline olefin polymer. The present invention also concerns preparation of said compositions by dynamic vulcanization or by a sequential combination of dynamic vulcanization and static curing. Static curing may occur, for example in a heated oven. The present invention further concerns the use of a non-peroxide cure package to accomplish said dynamic vulcanization.
Thermoplastic elastomers, which can be processed and fabricated by methods used for thermoplastics and do not require vulcanization to develop elastomeric properties, are known (see, for example, U.S. Pat. No. 3,265,765 as well as Hartman et al., "Butyl Grafted to Polyethylene Yields Thermoplastic Elastomer," Rubber World, October 1970, pp. 59-64).
Dynamic vulcanization is a process whereby a blend of plastic, rubber and rubber curative is masticated while curing the rubber. The term "dynamic" indicates the mixture is subjected to shear forces during the vulcanization step as contrasted with "static" vulcanization wherein the vulcanizable composition is immobile (in fixed relative space) during vulcanization. One advantage of dynamic vulcanization is that elastoplastic (thermoplastic elastomeric) compositions may be obtained when the blend contains the proper proportions of plastic and rubber. Dynamic vulcanization processes are described in U.S. Pat. Nos. 3,037,954, 3,806,558, 4,104,210, 4,116,914, 4,130,535, 4,141,863, 4,141,878, 4,173,556, 4,207,404, 4,271,049, 4,287,324, 4,288,570, 4,299,931, 4,311,628 and 4,338,413.
Known dynamic vulcanization processes are believed to be somewhat unsuitable for making soft compositions because as the rubber level rises the resulting compositions become less fabricable. In other words, the compositions give poor extrudates and, sometimes, cannot be extruded at all. Accordingly, there is a need for processes for preparing soft, extrusion-fabricable, thermoplastic elastomeric compositions.
U.S. Pat. No. 4,130,535 discloses thermoplastic vulcanizates or blends of polyolefin resin and monoolefin copolymer rubber which are processable in the same manner as thermoplastics even though the rubber is fully cured. The thermoset state is avoided by simultaneously masticating and curing the blends. The blends comprise about 25-95 percent by weight of the resin and about 75-5 percent by weight of the rubber. Oil extended vulcanizates have a ratio of 35 to 65 percent of the resin and about 65 to 35 percent of the rubber. Peroxide, azide and sulfur vulcanizing agents may be used to effect curing of the rubber. Typical monoolefin copolymer rubbers include saturated EPM (ethylene-propylene rubbers) or unsaturated EPDM (ethylene-propylene-diene terpolymer rubbers).
U.S. Pat. No. 4,594,390 teaches that improved thermoplastic elastomer materials are obtained when a composition comprising polypropylene, an EPDM rubber, an extender oil and a curative is masticated at a shear rate of at least 2000 sec.sup.-1. Suitable results are obtained with shear rates of 2500 to 7500 sec.sup.-1.
U.S. Pat. No. 4,207,404 discloses thermoplastic elastomer compositions prepared by dynamic vulcanization of blends of chlorinated polyethylene and nylon in the presence of a peroxide vulcanizing agent.
U.S. Pat. No. 3,806,558 discloses partially cured blends of a monoolefin copolymer rubber, such as those disclosed in U.S. Pat. No. 4,130,535, and a polyolefin plastic, usually polyethylene or polypropylene. The blend is mixed with a small amount of curative, and subjected to curing conditions while working the mixture dynamically.
A. Y. Coran, R. P. Patel and D. Williams, in an article entitled "Rubber-Thermoplastic compositions. Part V. Selecting Polymers for Thermoplastic Vulcanizates," Rubber Chemistry and Technology, Vol. 55, 116 (1982), describe approximately one hundred thermoplastic vulcanizate compositions, based on nine kinds of thermoplastic resin and eleven kinds of rubber. All compositions contain sixty parts of rubber and forty parts of plastic. They prepare these compositions by melt mixing the plastic, rubber and other components in a Brabender or Haake mixer. Generally, the plastic, rubber and other components of the composition, except for curatives, are mixed at controlled elevated temperatures (Table I) for about 2-6 minutes during which time the plastic melts and a blend is formed with the rubber. After blend formation, curatives are added to crosslink the rubber, and mixing is continued until a maximum consistency or mixing torque is observed. Each composition is removed from the mixer and then remixed for an additional minute in the molten state to insure uniformity of the mixture. One of the rubber materials is chlorinated polyethylene (CPE). The plastic materials, listed in Table I on page 117, include polypropylene (PP), polyethylene (PE), polystyrene (PS), an acrylonitrile-butadiene-styrene polymer (ABS), a styrene-acrylonitrile copolymer (SAN), polymethyl methacrylate (PMMA), poly-tetramethylene terephthalate (PTMT), Nylon-6,9 (PA) and polycarbonate (PC). One of the mechanical properties, tension set (ASTM D412-66), is determined by stretching 51 mm long specimens to 102 mm for 10 minutes then by measuring set after 10 minutes relaxation. Chlorinated polyethylene compositions are cured by peroxides, specifically 2,5-dimethyl-2,5-bis(t-butyl peroxy)hexane. Tension set values abstracted from Table IX at page 125 are as follows: (a) CPE/PP--55%; (b) CPE/PE--58%; (c) CPE/ABS--65%; (d) CPE/ABS--91%; (e) CPE/PMMA--82%; (f) CPE/PTMT--40%; (g) CPE/PA--59%; and (h) CPE/PC--85%. They note that the 40% value may not be accurate because the CPE is insufficiently stable to withstand processing at the high melt temperatures for PTMT.
SUMMARY OF THE INVENTION
One aspect of the present invention is a process for preparing a thermoplastic elastomer material from a blend of an amorphous chlorinated polyethylene and a crystalline thermoplastic polymer, the process comprising:
a. forming a heat-plastified, substantially uniform admixture comprising an amorphous chlorinated polyethylene, a plasticizing material compatible with the chlorinated polyethylene, a crystalline thermoplastic polymer, and a basic material; and
b. dispersing a vulcanizing material for the chlorinated polyethylene throughout the admixture while mixing said admixture at a temperature sufficient to activate the vulcanizing package without substantially degrading any component of the composition and for a period of time sufficient to cure substantially all of the chlorinated polyethylene, the vulcanizing material comprising (1) a derivative of 2,5-dimercapto-1,3,4-thiadiazole or (2) 2,5-dimercapto-1,3,4-thiadiazole and an activator material.
A related aspect of the present invention is a process for preparing a thermoplastic elastomer material from a blend of an amorphous chlorinated polyethylene and a crystalline thermoplastic polymer, the process comprising:
a. forming a heat-plastified, substantially uniform admixture comprising an amorphous chlorinated polyethylene, a plasticizing material compatible with the chlorinated polyethylene, a crystalline thermoplastic polymer and a basic material;
b. dispersing a vulcanizing material for the chlorinated polyethylene throughout the admixture while mixing said admixture at a temperature sufficient to activate the vulcanizing package without substantially degrading any component of the composition and for a period of time sufficient to partially cure the chlorinated polyethylene, the vulcanizing package comprising (1) a derivative of 2,5-dimercapto-1,3,4-thiadiazole or (2) 2,5-dimercapto-1,3,4-thiadiazole and an activator material; and
c. completing vulcanization of the chlorinated polyethylene via static curing.
The present invention also relates to the thermoplastic elastomer materials so prepared. These materials suitably have a tension set value, at 100% elongation (ASTM D412), of less than about 50%. Materials having tension set values of greater than 50% are believed to be unsuitable for use as elastomers. Thus, a third aspect of the present invention is a thermoplastic elastomeric composition comprising a blend of one hundred parts by weight of an amorphous chlorinated polyethylene resin, from about twelve to about one hundred fifty parts by weight of a crystalline thermoplastic polyolefin resin, and plasticizing material in an amount of from about five to about one hundred fifty parts by weight, the composition being processable in an internal mixer to provide a product which forms an essentially continuous sheet following transfer, with the resin components in a heat-plastified state, to the rotating rolls of a rubber mill.
DESCRIPTION OF PREFERRED EMBODIMENTS
The crystalline thermoplastic polymer is a solid, high molecular weight, resinous plastic material made by polymerizing olefins such as ethylene, propylene, butene-1, pentene-1, 4-methylpentene, and the like by conventional processes. Illustrative polymers include low density polyethylene (0.910 to 0.925 grams per cubic centimeter (g/cc)), medium density polyethylene (0.926 to 0.940 g/cc) or high density polyethylene (0.941 to 0.965 g/cc), whether prepared by high pressure processes or low pressure processes. Polyesters such as polyethylene terephthalate may also provide suitable results. Particularly suitable polymers include the crystalline forms of polypropylene. Crystalline block copolymers of ethylene and propylene (which are plastics distinguished from amorphous, random ethylene-propylene elastomers) can also be used. Included among the polyolefin resins are the higher alpha-olefin modified polyethylenes and polypropylenes (see, "Polyolefins," N. V. Boenig, Elsevier Publishing Co., N.Y. 1966).
Materials other than crystalline thermoplastic polymers may be used in conjunction with the amorphous chlorinated polyethylene provided such materials are mechanically compatible with the chlorinated polyethylene. "Mechanically compatible", as used herein, means that the polymers form a two phase mixture that does not undergo substantial delamination. Illustrative materials believed to meet this criterion include glassy polymers such as polycarbonates, styrene-acrylonitrile copolymers and terpolymers of acrylonitrile, butadiene and styrene.
Chlorinated polyethylene starting materials suitable for purposes of the present invention are finely-divided particles which must meet four physical property criteria. First, the materials must have a weight average molecular weight of from about 40,000 to about 300,000. Second, the materials must have a chemically combined chlorine content of from about 20 to about 48 percent by weight of polymer. Third, the materials must have a 100 percent modulus, measured in accordance with ASTM Test D-412, from about 0.5 to about 4.8 MPa. Fourth, the materials must have a relative crystallinity of from about 0 to about 15 percent, preferably from about 0 to about two percent.
Chlorinated polyethylene materials meeting the aforementioned physical property criteria can be prepared by a chlorinated procedure of the type disclosed in U.S. Pat. No. 3,454,544, the teachings of which are incorporated herein by reference thereto.
Satisfactory chlorinated polyethylene resins are readily obtained by practice of a chlorination procedure which comprehends suspension chlorination, in an inert medium, of a finely divided, essentially linear polyethylene or olefin interpolymer. The interpolymer contains at least about 90 mole percent ethylene with the remainder being one or more ethylenically unsaturated monomers polymerizable therewith. The polymer is first chlorinated at a temperature below its agglomeration temperature for a period of time sufficient to provide a partially chlorinated polymer having a chlorine content of from about 2 to 23 percent chlorine, based on the total weight of polymer. This is followed by sequential suspension chlorination of the partially chlorinated polymer, in a particulate form, at a particular temperature. The particular temperature is, with respect to the olefin interpolymer, above its agglomeration, temperature but at least about 2.degree. Centigrade below its crystalline melting point. Sequential chlorination is continued for a period of time sufficient to provide a chemically combined chlorine content of up to about 48 percent by weight of polymer.
Useful ethylenically unsaturated monomers include non-aromatic hydrocarbon olefins having three or more carbon atoms such as propylene, butene-1, 1,4-hexadiene, 1,5-hexadiene, octene-1, 1,7-octadiene, 1,9-decadiene and the like; substituted olefins such as acrylic acid, acrylic acid esters and the like; alkenyl aromatic compounds such as styrene and its derivatives, and other known polymerizable materials.
The temperature at which chlorination normally leads to agglomeration of polymer particles depends to a large extent on the nature and molecular weight of the polymer to be chlorinated. In the case of crystalline and predominantly straight chain polyethylenes having a branching of the chains of less than one methyl group per 100 carbon atoms and a density of at least 0.94 grams per cubic centimeter, the temperature is above 95.degree. Centigrade, in particular above 100.degree. Centigrade or even about about 110.degree. Centigrade. In the case of polyethylenes having a relatively marked branching of the chains and a lower density, the temperature is lower, about 65.degree. Centigrade.
The temperature employed in the sequential chlorination must be greater than that employed in the initial chlorination in order to prevent (a) retention of excessive undesirable crystallinity and (b) formation of nonuniformly chlorinated polymer. The temperature employed in the sequential chlorination must also be below the crystalline melting point of the polymer being chlorinated in order to prevent accelerated particle size growth and development of undesirable agglomeration of polymer particles.
After a polyolefinic material has been suspension chlorinated to a desired degree, it may easily be filtered from suspension in the inert suspending liquid, washed and dried to prepare it for subsequent use.
The present invention is not restricted to chlorinated polyethylene resins prepared by suspension or slurry chlorination procedures. Solution chlorination and bulk, or fluidized bed, chlorination procedures may also be used provided the polymers produced thereby meet the aforementioned requirements with regard to chlorine content and residual crystallinity.
The thermoplastic elastomers or vulcanizates of the present invention are suitably cured with a cure package comprising a basic material and 2,5-dimercapto-1,3,4-thiadiazole or a derivative thereof. These cure packages are disclosed in U.S. Pat. Nos. 4,128,510 and 4,288,576, the teachings of which are incorporated herein by reference thereto.
Peroxide cure packages are believed to be unsuitable for use in curing blends as disclosed herein, particularly where the crystalline olefin polymer is polypropylene. Physical properties and handling characteristics of the blends indicate either a lack of sufficient crosslinking or at least partial degradation of the polypropylene.
Illustrative derivatives of 2,5-dimercapto-1,3,4-thiadiazole include: ##STR1## wherein X is a substituent selected from hydrogen, --CRR'OH, --(CH.sub.2 --CH--O).sub.n H, ##STR2## where m is an integer of from 2 to 10; n is an integer from 1 to 5; R and R' are selected from hydrogen, alkyl groups containing 1-8 carbon atoms, and aryl, alkaryl or aralkyl groups containing 6 to 8 carbon atoms; R.sup.2 is an alkyl group containing 1-17 carbon atoms, an aryl group containing one or two rings, an alkaryl group containing 7-14 carbon atoms, an aralkyl group containing 7-8 carbon atoms or a cyclohexyl group; and R.sup.3 is an alkyl group containing 1-8 carbon atoms. X' can be the same as X with the exception of hydrogen and Y is zinc, lead, ##STR3## where R.sup.4 is an alkylene or alkenylene group containing 1-8 carbon atoms, or a cycloalkylene, arylene or a alkarylene group containing 6-8 carbon atoms; z is 0 or 1; and R.sup.5 is an alkylene group containing 2-8 carbon atoms or a phenylene, methylphenylene or methylenediphenylene group.
Basic materials suitable for use in conjunction with derivatives of 2,5-dimercapto-1,3,4-thiadiazole include inorganic materials such as basic metal oxides and hydroxides and their salts with weak acids, such as, for example, magnesium hydroxide, magnesium oxide, calcium oxide, calcium hydroxide, barium oxide, barium carbonate, sodium phenoxide and sodium acetate. These basic materials also serve as heat stabilizers for chlorinated polyethylene. Thus, they are beneficially admixed with the chlorinated polyethylene before the polymer blend is converted to a heat-plastified admixture rather than in conjunction with the thiadiazole derivative. Additional basic material may, if desired, be added together with the thiadiazole derivative. Other basic materials may also be used so long as they do not promote degradation of one of the components of the blend or deactivate the vulcanizing materials. The basic material is preferably magnesium oxide or magnesium hydroxide.
Basic or activator materials suitable for use in conjunction with 2,5-dimercapto-1,3,4-thiadiazole include (1) amines having a boiling point above about 110.degree. C., and a pK value below about 4.5; (2) salts of amines having pK values below about 4.5 with acids having pK values above about 2.0; (3) quaternary ammonium hydroxides and their salts with acids having pK values above about 2.0; (4) diphenyl- and ditolylguanidines; and (5) the condensation product of aniline and at least one mono-aldehyde containing one to seven carbon atoms, in combination with at least an equal amount of an inorganic base. The term "pK value" refers to the dissociation constants of bases and acids in aqueous solution. Representative values are shown in the Handbook of Chemistry and Physics, 45th Edition, The Chemical Rubber Co., page D-76 (1964). As noted in the preceding paragraph, a certain amount of a basic material such as magnesium oxide or magnesium hydroxide must also be present to heat stabilize the chlorinated polyethylene.
The plasticizing material is suitably selected from the group consisting of trimellitate esters, phthalate esters, aromatic oils and polyesters of dicarboxylic acids containing from about two to about ten carbon atoms. The plasticizing material is desirably trioctyl trimellitate.
The ingredients save for the vulcanizing material are mixed at a temperature sufficient to soften the crystalline thermoplastic polymer or, more commonly, at a temperature above its melting point if the polymer is crystalline at ordinary temperatures. Blending is carried out for a time sufficient to form a generally uniform blend of the components. It is accomplished by any one of a number of conventional techniques, for example, in an internal mixer, two-roll mill or extruder. After the resin and rubber are intimately mixed, the vulcanizing material is added. Heating and masticating the blend components at vulcanization temperatures are generally adequate to complete curing in a few minutes. If shorter vulcanization times are desired, higher temperatures may be used, provided they are low enough to preclude substantial degradation of the chlorinated polyethylene.
Suitable vulcanization temperatures range from about the melting temperature of the crystalline thermoplastic polymer (about 130.degree. C. in the case of polyethylene and about 175.degree. C. in the case of polypropylene) to 250.degree. C. or more. Typically, the range is from about 150.degree. C. to 225.degree. C. A preferred range of vulcanization temperatures is from about 180.degree. to about 200.degree. C. Thermoplastic vulcanizates are beneficially prepared by continuously mixing the compositions, after the vulcanizing material is added, until vulcanization is complete.
If desired from an economic point of view, completion of vulcanization may be accomplished by static vulcanization provided sufficient curing by dynamic vulcanization has occurred before static vulcanization begins. If insufficient dynamic vulcanization occurs, an unprocessable thermoset vulcanizate may be obtained.
Physical property values from a hybrid of dynamic vulcanization and static vulcanization, where adequate dynamic vulcanization has occurred, do not differ appreciably from those obtained from blends cured solely by dynamic vulcanization. By way of illustration, sufficient dynamic vulcanization occurs in as little as one minute in a heated mixer operating at a temperature of about 400.degree. F. (about 204.degree. C.) if the components of the blend are premixed. Without premixing, five minutes or even longer may be required to achieve sufficient dynamic vulcanization in such a heated mixer. If appreciable static curing occurs before the rubber is dispersed and the thermoplastic becomes a continuous phase, an unprocessable thermoset vulcanizate may be obtained.
A convenient measure of the state of cure of the thermoplastic elastomer compositions of the present invention is obtained by comparing the tensile strength of the blend before and after dynamic vulcanization. The dynamically vulcanized blend using a thiadiazole cure package suitably has a tensile strength of about 1.3 megapascals (MPa) and desirably 3.4 MPa or more greater than that of the unvulcanized blend or the peroxide cured blend.
The properties of the thermoplastic vulcanizates of this invention may be modified, either before or after vulcanization, by adding ingredients which are conventional in the compounding of chlorinated polyethylene elastomers, polyolefin resins and blends thereof. Skilled artisans will recognize, however, that chlorinated polyethylene compounding additives generally must be added before vulcanization if they are to have an effect upon the chlorinated polyethylene. The timing of addition is not as critical for addition of ingredients to the thermoplastic portion of the materials of the present invention.
Examples of suitable ingredients or additives include various carbon blacks, alumina, silica, titanium dioxide, calcium carbonate, colored pigments, clays, zinc oxide, stearic acid, accelerators, vulcanizing agents, sulfur, stabilizers, antioxidants, antidegradants, processing aids, adhesives, tackifiers, plasticizers, processing aids such as lubricants and waxes, prevulcanization inhibitors, discontinuous fibers such as glass fibers and wood cellulose fibers, and extender oils. The amounts used depend, at least in part, upon the quantities of other ingredients in the composition and the properties desired from the composition. Minor amounts of other saturated and unsaturated polymers such as alpha-olefins may be added to reduce the cost or modify the properties of the composition.
The addition of carbon black, or an extender oil or both is recommended, particularly if accomplished prior to dynamic vulcanization. Carbon black improves the tensile strength and extender oil can improve the resistance to oil swell, heat stability, hysteresis, cost and permanent set of the thermoplastic vulcanizate. The addition of extender oil can also improve processability.
Aromatic, naphthenic and paraffinic extender oils provide satisfactory results so long as they are used in amounts which do not exceed their limits of compatibility with chdlorinated polyethylene. Suitable extender oils are identified in Rubber World Blue Book, Materials and Compounding Ingredients for Rubber (1975), pages 145-190. The quantity of extender oil added depends upon the properties desired. The upper limit, which depends upon the compatibility of a particular oil and blend ingredients, is exceeded when excessive exudation of extender oil occurs. Typically, 5-150 parts by weight extender oil are added per 100 parts by weight of chlorinated polyethylene. Commonly, from about 30 to about 125 parts by weight of extender oil are added per 100 parts by weight of chlorinated polyethylene present in the blend with quantities of from about 70 to 100 parts by weight of extender oil per 100 parts by weight of chlorinated polyethylene being preferred.
Typical additions of carbon black comprise about 40-250 parts by weight of carbon black per 100 parts by weight of chlorinated polyethylene and usually about 20-100 parts by weight carbon black per 100 parts by weight of chlorinated polyethylene. The amount of carbon black which can be used depends, at least in part, upon the type of carbon black and upon the amount of extender oil to be used.
Thermoplastic elastomeric vulcanizates prepared as described herein are useful for making a variety of articles such as tires, hoses, belts, gaskets, moldings and molded parts. They are particularly useful for making articles by extrusion, injection molding and compression molding techniques. They also are useful for modifying thermoplastic resins in general and polyolefin resins in particular. The vulcanizates are suitably blended with thermoplastic resins using conventional mixing equipment. The properties of the modified resin depend upon the amount of vulcanizate blended. Generally, the amount of vulcanizate is sufficient to provide from about 5 to 25 parts by weight of chlorinated polyethylene per hundred parts by weight of the modified resin.

The following examples are for purposes of illustration only and are not to be construed as limiting the scope of the present invention. All parts and percentages are by weight unless otherwise specified. Arabic numerals are used to identify examples representing the present invention whereas alphabetic characters are used to designate comparative examples.
SAMPLE PREPARATION
A 1450 cubic centimeter (cc) capacity Banbury mixer is used to provide initial melt compounding of all blends and, when appropriate curative components are added and activated, at least partial curing of said blends. Further mixing and, if needed, completion of curing takes place when the contents of the Banbury mixer are placed on a heated two roll mill. Curing may also be completed in a static cure oven.
A. Multiple Step Banbury Mix Procedure
1. Prepare a rubber masterbatch by adding chlorinated polyethylene, stabilizers, fillers, plasticizers and other additives to the Banbury mixer while it is operating at low speed (about 77 revolutions per minute (rpm)) and cooling water is circulating through the front and rear rotors, right and left sides and fixed sections of the Banbury mixer. As noted hereinabove, the base to be used in conjunction with the vulcanizing material may also function as the stabilizer. The amounts of masterbatch components are sufficient to fill the mixing cavity. Mixing continues for about four minutes at which time the temperature of the contents reaches 325.degree. Fahrenheit (.degree.F.) (approximately 163.degree. C.).
2. Remove part of the masterbatch, replace it with an amount of crystalline thermoplastic polymer and continue mixing for about five minutes at a temperature of about 350.degree. F. (approximately 176.degree. C.). The temperature of the contents is controlled by varying the mixer speed.
3. Remove the blend from the Banbury mixer and place it on a two roll rubber compounding mill operating at a set temperature of about 70.degree. F. (approximately 21.degree. C.) with a gap between the rolls of about 200 mils (5 millimeters (mm)).
4. After cooling the blend on the two roll mill for a period of about two minutes, add components to be used in vulcanizing the blend (also known as the "cure package") and continue mixing for a period of about two minutes.
5. Remove the roll milled blend (also known as "the blanket") from the two roll mill, cut it into strips and add the strips to the Banbury mixer which is operating at a set temperature of from about 350.degree. F. (approximately 176.degree. C.) to about 370.degree. F. (approximately 188.degree. C.). Mixing and curing of the CPE continues for about seven minutes with temperature control as in step 2. This period of time is generally sufficient to completely cure the CPE component of the blend.
6. Remove the contents of the Banbury mixer and mix for two minutes on a hot two roll mix (heated with 150 pounds per square inch (psi) steam) with a gap between the rolls of about 200 mils (5 millimeters (mm)). This final mixing on the roll mill is done to assure that uniform samples are used to prepare compression molded samples for testing. Remove the contents from the mill in the form of a sheet having a thickness of about 65 mils (approximately 1.7 mm).
7. Compression mold the sheets to a thickness of 60 mils (approximately 1.5 mm) using a heated (372.degree. F. (approximately 189.degree. C.)) press. The press and its contents are first preheated with no applied force for two minutes. The contents are then pressed for three minutes with an applied force of twenty tons, cooled for four minutes with an applied force of twenty tons and then removed from the press after the force is relieved. The compression molded sheets are used for physical property characterization.
B. Single Load Banbury Mix Procedure
1. Same as step 1 of the Multiple Step Banbury Mix Procedure except that the mixer is not completely filled with rubber masterbatch components. In other words, there is sufficient room to add the crystalline thermoplastic polymer without the necessity of removing a portion of the masterbatch.
2. Add an amount of crystalline thermoplastic polymer and continue mixing for about five minutes at a temperature of about 350.degree. F. (approximately 176.degree. C.). The amount is generally sufficient to fill the mixer. The temperature of the contents is controlled by varying the mixer speed.
3. Add the vulcanizing material to the blend while continuing mixing. The vulcanizing material is placed in a small bag formed from an ethylene/acrylic acid copolymer commercially available from The Dow Chemical Company under the trade designation Primacor.TM.. The bag is used to minimize, if not eliminate, loss of vulcanizing material to the wall of the mixer. Mixing and curing continues for about seven minutes at a temperature of from about 350.degree. F. to about 370.degree. F. (from about 176.degree. C. to about 188.degree. C.). As noted herein, at step 5 of the Multiple Step Procedure, this period of time is generally sufficient to completely cure the CPE component of the blend.
4. Same as step 6 of the Multiple Step Banbury Mix Procedure.
5. Same as step 7 of the Multiple Step Banbury Mix Procedure.
Test Procedures
The following American Society for Testing and Materials (ASTM) Tests are used to characterize the physical properties of materials prepared in accordance with procedures A and B above:
Specific Gravity: ASTM Method D792
Hardness: ASTM Method D2240
Tensile Strength: ASTM Method D412
Elongation: ASTM Method D412
Modulus: ASTM Method D412
Tension Set: ASTM Method D412
Compression Set: ASTM Method D395B
Oil Resistance: ASTM Method D471
Heat Resistance: ASTM Method D573
EXAMPLES 1-3
CPE/PP Thermoplastic Elastomer
Using the Multiple Step Banbury Mix Procedure (Procedure A) or the Single Load Banbury Mix Procedure (Procedure B), sample sheets are prepared from the composition shown in Table I. In Example 1, the amount of trioctyl trimellitate is 85 parts and the amount of polypropylene is 56.0 parts. In Examples 2 and 3, the amount of trioctyl trimellitate is 100 parts and the amount of polypropylene is 59.9 parts.
Physical property test values obtained from said sample sheets are summarized in Table II.
TABLE I______________________________________EXAMPLE 1 COMPOSITIONParts/HundredParts of CPE Component Description/Source-Purpose______________________________________30 carbon black N330 - filler material5.2 hydrated amorphous silica, commercially available from PPG Industries, Inc. under the trade designation HiSil .TM. 223 - filler material5.2 magnesium oxide, commercially available from Elastochem Inc. under the trade designation Maglite .TM. D - activator85 or 100 trioctyltrimellitate - oil extender100 chlorinated polyethylene, commercially available from The Dow Chemical Company under the trade Designation Tyrin .TM. CM0136 - rubber56.0 or 59.9 polypropylene, commercially available from Himont, Inc. under the trade desig- nation Pro-fax .TM. 6723 - thermoplastic3.0 5-mercapto-1,3,4-thiadiazole-2- thiobenzoate, commercially available from Hercules Inc. under the trade designation Echo-S .TM. curative0.9 condensation product of analine and butyraldehyde commercially available from R. T. Vanderbilt Co., Inc. under the trade designation Vanax .TM. 808 - curative accelerator______________________________________
TABLE II______________________________________Physical Property Data for Examples 1-3Process/Physical Property Physical Property Measured Value(Unit of Measure) Ex. 1 Ex. 2 Ex. 3______________________________________Process A A BSpecific Gravity 1.12 1.11 1.11Hardness, Shore A 80 78 82Ultimate Tensile 1128/7.8* 1087/7.5* 1192/8.2(psi/MPa)Elongation (%) 258* 292* 256100% Modulus (psi/MPa) 608/4.2* 548/3.8* 670/4.6200% Modulus (psi/MPa) 946/6.5* 836/5.8* 997/6.9Tension Set @ 100% Elong. 16 15 15Compression Set 60 63 65212.degree. F./70 HoursASTM Oil 2,250.degree. F./70 HoursVolume Swell (%) 8 5 4% Tensile Retained 66 62 79% Elong. Retained 80 57 69% 100% Mod. Ret. 86 99 91ASTM Oil 3,250.degree. F./70 HoursVolume Swell (%) 24 20 19% Tensile Retained 54 57 61% Elong. Retained 66 64 70% 100% Mod. Ret. 62 74 77______________________________________ *Average of two test samples
The data presented in Table II demonstrate that similar results are obtained by the single step and multi-step processes. The data also demonstrate that satisfactory results are obtained with two different levels of trioctyl trimellitate. Similar results are expected with other compositions and process variations which fall within the scope of the present invention.
EXAMPLE 4 AND COMPARATIVE EXAMPLES A-B
Cure System Comparison
Using the Single Load Banbury Mix Procedure (Procedure B), sample sheets are prepared from compositions similar to that shown in Table I. In Example 4 and Comparative Examples A and B, the amount of trioctyl trimellitate is 100 parts and the amount of polypropylene is 59.9 parts. In Example 4, the amount of accelerator is increased to 1.0 part. In Comparative Example A, no cure package is used and in Comparative Example B, curing is accomplished with a peroxide cure package. The peroxide cure package includes 6.0 parts of .alpha.-.alpha.'-bis(t-butylperoxy)diisopropylbenzene on Burgess KE Clay, commercially available from Hercules Inc. under the trade designation Vul-Cup.TM. 40KE and 2.0 parts of triallyl trimellitate (commercially available from C. P. Hall). Physical property test values obtaained from said sample sheets are summarized in Table III.
TABLE III______________________________________Cure System ComparisonProcess/Physical Property Physical Property Measured Value(Unit of Measure) Ex. 4 Comp Ex. A Comp Ex. B______________________________________Process B B BSpecific Gravity 1.11 1.10 1.12Hardness, Shore A 80 78 75Ultimate Tensile 1137/ 937/ 471/(psi/MPa) 7.8 6.5 3.2Elongation (%) 257 533 197100% Modulus (psi/MPa) 665/4.6 518/3.6 372/2.6200% Modulus (psi/MPa) 963/6.6 601/4.1 --Tension Set @ 100% 16 28 22Elong.Compression Set 56 87 90212.degree. F./70 HoursASTM Oil 2,250.degree. F./70 HoursVolume Swell (%) 5 13 21% Tensile Retained 69 51 51% Elong. Retained 65 24 21% 100% Mod. Ret. 96 84 --ASTM Oil 3,250.degree. F./70 HoursVolume Swell (%) 20 47 42% Tensile Retained 60 34 18% Elong. Retained 60 18 17% 100% Mod. Ret. 81 -- --______________________________________ -- not measured
The data presented in Table III demonstrate that physical properties are improved when the CPE/PP blends are cured with a thiadiazole cure. The data also demonstrate that physical properties are degraded when the blends are cured with a conventional peroxide cure package. Similar results are obtained with other compositions within the scope of the present invention.
COMPARISON EXAMPLES C-F
Commercial Thermoplastic Elastomer Physical Properties
In order to evaluate the potential suitability of the thermoplastic elastomers of the present invention, four commercially available thermoplastic elastomers are subjected to the same tests as Examples 1 and 2. Comparative Example C is Santoprene.TM. 201(73), commercially available from Monsanto Co. Comparative Example D is Santoprene.TM. 201(80), commercially available from Monsanto Co. Comparative Example E is Alcryn.TM. 1201B, an oil resistant thermoplastic elastomer commercial available from E. I. DuPont de Nemours & Co. Comparative Example F is Geolast.TM. 701, an oil resistant thermoplastic elastomer commercially available from Monsanto Co. The test results are presented in Table IV which follows. Example 1 is included in Table IV for ease of comparison.
TABLE IV______________________________________Physical Property ComparisonProcess/Physical Physical Property Measured ValueProperty (Unit Comp Comp Comp Compof Measure) Ex 1 Ex C Ex D Ex E Ex F______________________________________Specific Gravity 1.12 .968 .966 1.23 1.09Hardness, 80 76 80 65 80Shore AUlt. Tens. 1123/ 1451/ 1494/ 1796/ 1339/psi/MPa 7.8* 10.0 10.3 12.4 9.2Elongation % 258* 513 415 280 200 309 294100% Mod, 608/ 472/ 598/ 608/ 548/psi.MPa 4.2* 3.3 4.1 4.2* 3.8*200% Mod, 946/ 607/ 813/ 1162/ 1246/psi.MPa 6.5* 4.2 5.6 8.0* 8.6*Tension Setat 100% Elong. 16 15 10 6 12Compression Set 60 40 40 59 50212.degree. F./70 hoursLow Temp Britt .degree. C. -36 -60** -60** -35 -38ASTM Oil 2, 250.degree.F./70 HrVol Swell % 8 46 40 4 2% Tens Ret 66 68 77 103 97% Elong Ret 80 64 76 93 79% 100% Mod Ret 86 86 101 94 109ASTM Oil 3, 250.degree.F./70 HrVol Swell % 24 65 59 17 13% Tens Ret 54 61 74 82 71% Elong Ret 66 58 74 78 61% 100% Mod Ret 62 75 95 85 90______________________________________ *average of two test samples **reported by manufacturer
The data presented in Table IV demonstrate that the thermoplastic elastomers of the present invention compare favorably with commercially available materials in terms of physical properties such as tension set at 100% elongation, tensile, elongation, oil resistance and low temperature impact resistance.
EXAMPLES 5-9
Effect of Different Polypropylene on Properties
Using the Single Mix Procedure (Procedure B), sample sheets were prepared from a composition similar to that shown in Table I. The type and amount of filler materials, chlorinated polyethylene, curative and curative co-agent are the same. The amount of trioctyltrimellitate is one hundred parts. The following polypropylenes are used in amount of 59.9 parts: PP-A is Pro-fax.TM. 6723, 0.8 g/10 min. melt index; PP-B is Pro-fax.TM. 6524, 4.0 g/10 min. melt index; PP-C is Pro-fax.TM. 6324, 12.0 g/10 min. melt index; PP-D is Pro-fax.TM. 6301, 12.0 g/10 min. melt index--unstabilized; and PP-E is Pro-fax.TM. 6624, 35.0 g/10 min. melt index.
Physical property test values together with the type of polypropylene are shown in Table V.
TABLE V__________________________________________________________________________Effect of Different Types of Polypropylene on PropertiesProcess/Physical Property Physical Property Measured Value(Unit of Measure) Ex. 5 Ex. 6 Ex. 7 Ex. 8 Ex. 9__________________________________________________________________________PP Type A B C D ESpecific Gravity 1.11 1.11 1.11 1.11 1.11Hardness, Shore A 86 86 85 86 86Ultimate Tensile (psi/MPa) 1105/7.6 1107/7.6 978/6.7 926/6.4 657/4.5Elongation (%) 290 225 232 229 189100% Modulus (psi/MPa) 710/4.9 853/5.9 689/4.8 687/4.7 657/4.5200% Modulus (psi/MPa) 989/6.8 1057/7.3 879/6.1 886/6.1 --Tension Set @ 100% Elong. 25 24 27 26 23Compression Set 73 70 85 80 75212.degree. F./70 HrsASTM Oil 2, 250.degree. F./70 HrsVolume Swell (%) 4 4 5 4 3% Tensile Retained 62 49 42 50 46% Elong. Retained 45 36 35 37 34ASTM Oil 3, 250.degree. F./70 HrsVolume Swell (%) 21 21 24 23 19% Tensile Retained 52 44 36 39 39% Elong. Retained 44 36 29 22 24__________________________________________________________________________ -- cannot be measured
The data presented in Table V demonstrate that high molecular weight polypropylenes (e.g. Ex. 5) produce thermoplastic elastomer materials with higher tensile strength and elongation than lower molecular weight polypropylenes (Ex. 9). The higher molecular weight polypropylenes also have greater tensile strength and elongation values after exposure to oils even though percent property retention does not vary significantly. Similar results are obtained when samples are exposed to air oven aging as well as with other polymer blend compositions within the scope of the present invention.
EXAMPLES 10-15
Effect of Extender Oil Type Upon Physical Properties
Using the Single Load Banbury Mix Procedure (Procedure B) and, with two exceptions, the composition of Example 4, sample sheets are prepared for physical property testing. One exception is that, for Examples 10-15, the magnesium oxide is changed to a magnesium hydroxide commercially available under the trade designation Marinco.TM. H from Calgon. The second exception is in the type of extender oil. The extender oils are as follows: Example 10--TOTM; Example 11--a high boiling aromatic oil commercially available from R. E. Carroll under the trade designation Polyflo.TM. 1172 (hereinafter "AR-1"); Example 12--a high boiling aromatic oil commercially available from R. E. Carroll under the trade designation Sundex.TM. 8600T (hereinafter "AR-2"); Example 13--a high boiling aromatic oil commercially available under the trade designation Sundex.TM. 8125 (hereinafter "AR-3); Example 14--an aromatic oil commercially available from R. E. Carroll under the trade designation Sundex.TM. 790 (hereinafter "AR-4"); and Example 15--dioctyl phthalate (hereinafter "DOP"). Physical property test results are summarized in Table VI.
TABLE VI__________________________________________________________________________Effect of Extender Oil TypeProcess/Physical Property Physical Property Measured Value(Unit of Measure) Ex. 10 Ex. 11 Ex. 12 Ex. 13 Ex. 14 Ex. 15__________________________________________________________________________Type Oil TOTM AR-1 AR-2 AR-3 AR-4 DOPSpecific Gravity 1.11 1.15 1.10 1.12 1.10 1.11Hardness, Shor A 86 85 85 87 79 82Ultimate Tensile (psi/MPa) 1105/7.6 1292/8.9 923/6.4 1053/7.3 891/6.1 1016/7.0Elongation (%) 290 314 216 271 239 245100% Modulus (psi/MPa) 710/4.9 712/4.9 709/4.9 719/5.0 556/3.8 649/4.5200% Modulus (psi/MPa) 989/6.8 1035/7.1 899/6.2 940/6.5 789/5.4 909/6.3Tension Set @ 100% Elong. 25 30 28 28 16 16Compression Set 73 77 80 82 72 68212.degree. F./70 HrsASTM Oil 2, 250.degree. F./70 HrsVolume Swell (%) 2 2 9 5 2 4% Tensile Retained 62 55 51 54 72 59% Elong. Retained 45 41 42 39 53 44% 100% Mod. Ret. 75 84 -- 74 -- 88ASTM Oil 3, 250.degree. F./70 HrsVolume Swell (%) 20 22 27 23 19 21% Tensile Retained 52 43 48 45 58 50% Elong. Retained 44 34 50 38 58 50% 100% Mod. Ret. 67 73 57 64 77 69__________________________________________________________________________ -- not measured
The data presented in Table VI show that physical property values are generally acceptable for all types of extender oils. The aromatic oils are not as compatible as TOTM with the blends. As such, some bleeding to the surface is observed when aromatic oils are used. The aromatic oils also have less resistance to physical property degradation following thermal aging than TOTM. In addition, low temperature properties are poorer when aromatic oils are used rather than TOTM or DOP or other ester plasticizers. DOP suffers from a similar loss of physical properties following thermal aging. The loss of physical properties following thermal aging, while rendering such compounds unsuitable for high temperature applications such as are experienced in an automobile engine compartment, are not important if the compounds are subjected only to comparatively low temperatures. Similar results are expected with other compounds which are representative of the present invention.
EXAMPLES 16-34
Cure Program Variability
Using the composition of Example 4 except that the amount of polypropylene is 60 parts, a variety of cure programs using only dynamic curing (in the Banbury mixer) or a combination of dynamic curing and static curing (in a heated oven) are evaluated. Results of the evaluation are shown in Table VII.
TABLE VII__________________________________________________________________________Cure Program Variability, Examples 16-21 Example No. 16 17 18 19 20 21__________________________________________________________________________CURE PROGRAM (MINUTES)Mix Rubber Component 3 3 3 3 3 3Add PP then Mix 4 4 4 4 4 4Dynamic (Mixer) Cure Time 1 1 1 3 3 3Roll Mill Time 1 1 1 1 1 1Static (Oven) Cure Time 0 4 6 0 2 4Roll Mill Time 2 2 2 2 2 2Total Mixer Time 8 8 8 10 10 10Total Cure Time 1 5 7 3 5 7PHYSICAL PROPERTIESUltimate Tensile (psi/mPa) 1270/8.8 1293/8.9 1300/9.0 1224/8.4 1225/8.7 1312/9.0Elongation (%) 326 307 325 310 317 324100% Modulus (psi/mPa) 718/5.0 737/5.1 725/5.0 712/4.9 703/4.8 716/4.9200% Modulus (psi/mPa) 1014/7.0 1061/7.3 1031/7.1 980/6.8 988/6.8 1002/6.9Tension Set @ 100% Elong. 25 23 25 28 25 25Compression Set 69 69 68 73 83 78(212.degree. F./70 hrs)ASTM OIL #2, 250.degree. F./70 HrsVolume Swell % 5 4 5 6 7 6% Tensile Retained 58 64 51 52 46 57% Elongation Retained 33 44 28 33 27 41ASTM OIL #3, 250.degree. F./70 HrsVolume Swell % 22 22 23 24 25 24% Tensile Retained 49 51 50 43 43 48% Elongation Retained 36 44 40 36 34 44__________________________________________________________________________Cure Program Variability, Examples 22-27 Example No. 22 23 24 25 26 27__________________________________________________________________________CURE PROGRAM (MINUTES)Mix Rubber Component 3 3 3 3 0 0Add PP then Mix 4 4 4 4 4 4Dynamic (Mixer) Cure Time 5 5 5 7 1 1Roll Mill Time 1 1 1 1 1 1Static (Oven) Cure Time 0 2 4 0 0 2Roll Mill Time 2 2 2 2 0 0Total Mixer Time 12 12 12 14 5 5Total Cure Time 5 7 9 7 1 3PHYSICAL PROPERTIESUltimate Tensile (psi/mPa) 1211/8.3 1274/8.8 1206/8.3 1290/8.9 1197/8.3 1218/8.4Elongation (%) 292 318 296 300 276 290100% Modulus (psi/mPa) 703/4.8 723/5.0 692/4.8 764/5.3 750/5.2 722/5.0200% Modulus (psi/mPa) 986/6.8 999/6.9 966/6.7 1033/7.1 1032/7.1 1003/6.9Tension Set @ 100% Elong. 28 28 25 23 25 25Compression Set 69 74 74 74 83 86(212.degree. F./70 hrs)ASTM OIL #2, 250.degree. F./70 HrsVolume Swell % 6 6 5 7 6 7% Tensile Retained 52 58 55 59 52 46% Elongation Retained 36 38 41 45 34 28ASTM OIL #3, 250.degree. F./70 HrsVolume Swell % 24 25 24 24 24 25% Tensile Retained 44 47 47 44 41 37% Elongation Retained 38 40 41 36 32 28__________________________________________________________________________Cure Program Variability, Examples 28-34 Example No. 28 29 30 31 32 33 34__________________________________________________________________________CURE PROGRAM (MINUTES)Mix Rubber Component 0 0 0 0 0 0 0Add PP then Mix 4 4 4 4 4 4 4Dynamic (Mixer) Cure Time 1 3 3 3 5 5 5Roll Mill Time 1 1 1 1 1 1 1Static (Oven) Cure Time 4 0 2 4 0 2 4Roll Mill Time 0 0 0 0 0 0 0Total Mixer Time 5 7 7 7 9 9 9Total Cure Time 5 3 5 7 5 7 9PHYSICAL PROPERTIESUltimate Tensile (psi/mPa) 1131/7.8 1246/8.6 1265/8.7 1236/8.5 1266/8.7 1300/9.0 1300/9.0Elongation (%) 266 261 260 244 268 284 281100% Modulus (psi/mPa) 705/4.9 784/5.4 765/5.3 790/5.4 760/5.2 776/5.3 793/5.5200% Modulus (psi/mPa) 983/6.8 1097/7.6 1085/7.5 1105/7.6 1084/7.5 1087/7.5 1084/7.5Tension Set @ 100% Elong. 25 25 25 23 25 25 25Compression Set (212.degree. F./70 hrs) 77 71 73 69 73 73 70ASTM Oil #2, 250.degree. F./70 HrsVolume Swell % 7 7 6 6 6 7 7% Tensile Retained 50 56 47 60 53 52 54% Elongation Retained 29 38 31 47 40 37 39ASTM Oil #3, 250.degree. F./70 HrsVolume Swell % 24 25 24 23 23 24 25% Tensile Retained 44 48 49 49 38 46 47% Elongation Retained 39 46 48 49 32 44 42__________________________________________________________________________ -- not measured
The data presented in Table VII demonstrate that a combination of dynamic curing and static curing provides results in terms of physical properties which are generally equivalent to those obtained with dynamic curing, e.g. Example 18 versus Example 25. The reduction in mixer time corresponds to a reduction in cost of the resulting cured blend.
EXAMPLES 35-38
Effect of CPE Feedstock Melt Index Upon Physical Properties
By duplicating the composition of Example 5 save for the type of CPE, samples are prepared for physical property testing. All of the CPE's have a chemically combined chlorine content of 36 percent by weight of polymer and a heat of fusion of 0.2 calories per gram. They differ primarily in terms of the melt index of the feedstock from which they are prepared. Melt index is determined in accordance with ASTM D-1238, condition 190/2.16. In Example 35, the CPE is prepared from a 0.1 decigram per minute feedstock and is commercially available from The Dow Chemical Company under the trade designation TYRIN.TM. 3615. In Example 36, the CPE is prepared from a 0.3 decigram per minute feedstock and is commercially available from The Dow Chemical Company under the trade designation TYRIN.TM. CM0136. In Example 37, the CPE is prepared from a 1.0 decigram per minute feedstock and is commercially available from The Dow Chemical Company under the trade designation TYRIN.TM. CM552. In Example 38, the CPE is prepared from a 6.0 decigram per minute feedstock and is commercially available from The Dow Chemical Company under the trade designation TYRIN.TM. CM0636. The physical property data are summarized in Table VIII.
TABLE VIII______________________________________CPE FEEDSTOCK MELT INDEX VARIATIONProcess/PhysicalProperty Physical Property Measured Value(Unit of Measure) Ex. 35 Ex. 36 Ex. 37 Ex. 38______________________________________Specific Gravity 1.11 1.11 1.11 1.11Hardness, Shore A 83 86 85 87Ultimate Tensile 1330/9.2 1105/7.6 1015/7.0 812/5.6(psi/MPa)Elongation (%) 292 290 266 167100% Modulus 689/4.8 710/4.9 695/4.8 720/5.0(psi/MPa)200% Modulus 1002/6.9 989/6.8 904/6.2 --(psi/MPa)Tension Set @ 100% 25 25 29 30Elong.Compression Set 69 73 80 77212.degree. F./70 HoursLow Temperature -37 -32 -33 -35Brittleness .degree.C.ASTM Oil 2, 250.degree. F./70HrsVolume Swell (%) 7 4 16 11% Tensile Retained 53 62 46 46% Elong. Retained 49 45 45 44ASTM Oil 3, 250.degree. F./70HrsVolume Swell (%) 27 21 38 24% Tensile Retained 43 52 35 46% Elong. Retained 42 44 33 44______________________________________ -- not measured
The data presented in Table VIII highlight three benefits from decreasing the feedstock melt index. First, the tensile strength of the vulcanized blend increases. Second, the tensile set and compression set of the vulcanized blend decrease. Finally, the resistance to oils increases. Similar results are obtained with other compounds which are representative of the present invention.
EXAMPLES 39-42 AND COMPARATIVE EXAMPLE G
Effect of Thermoplastic Polymer Amount Upon Physical Properties
Using the composition of Example 5, save for the amount of polypropylene, samples are prepared for physical property testing. Table IX includes the amount of polypropylene in parts per hundred parts of chlorinated polyethylene as well as in terms of percent by weight of composition. Table IX also displays data from the physical property testing.
TABLE IX__________________________________________________________________________Effect of Varying the Amount of Thermoplastic Polymer AmountProcess/Physical Property Physical Property Measured Value(Unit of Measure) Ex. 39 Ex. 40 Ex. 41 Ex. 42 Comp Ex. g__________________________________________________________________________Polypropylene FractionParts/100 parts CPE 12 41 78 126 191% of Composition Wt. 4.8 14.4 24.2 34.0 43.9PHYSICAL PROPERTY:Specific Gravity 1.16 1.13 1.09 1.06 1.04Hardness, Shore A 43 72 89 94 98Elongation (%) 303 310 272 247 293Tension Set @ 100% Elong. 10 20 35 45 50Ultimate Tensile (psi/MPa) 786/5.4 965/6.6 1248/8.6 1451/10.0 1796/12.4100% Modulus (psi/MPa) 227/1.6 442/3.0 823/5.7 1132/7.8 1496/10.3ASTM Oil 2, 250.degree. F./70 HrsVolume Swell (%) 4 6 6 7 7% Tensile Retained 77 61 64 83 96% Elong. Retained 63 39 37 53 53__________________________________________________________________________
A review of the data presented in Table IX show that thermoplastic elastomer materials result when polypropylene comprises from about five to about thirty-five percent of the composition weight (twelve to 126 parts per hundred parts of chlorinated polyethylene). When the polypropylene fraction increases to about forty-four percent of the composition weight (191 parts per hundred parts of chlorinated polyethylene), the tension set at 100% elongation reaches 50. As noted herein, a value of 50 or greater generally indicates a material unsuitable for use as an elastomer. As such, an upper limit on the amount of this type of polypropylene falls within the range of 126 to 191 parts per hundred parts of chlorinated polyethylene. When the polypropylene fraction falls below about five percent (about twelve parts per hundred parts of chlorinated polyethylene), the dynamically vulcanized composition exhibits characteristics of a thermoplastic elastomer notwithstanding some mold shrinkage when compression molded samples are prepared.
Similar results are expected from other compositions representative of the present invention. Although upper and lower limits on the amount of thermoplastic polymer may vary with the type of polymer, satisfactory results are readily attainable without undue experimentation.

Number	Name	Date
3758643	Fischer	Sep 1973
3806558	Fischer	Apr 1974
3835201	Fischer	Sep 1974
4104210	Coran et al.	Aug 1978
4128510	Richwine	Dec 1978
4130535	Coran et al.	Dec 1978
4141878	Coran et al.	Feb 1979
4207404	Coran et al.	Jun 1980
4288576	Richwine	Sep 1981
4480074	Wang	Oct 1984
4503192	McShane et al.	Mar 1985
4594390	Abdou-Sabet et al.	Jun 1986
4694042	McKee et al.	Sep 1987
4694049	Morita et al.	Sep 1987
4707519	Forti et al.	Nov 1987

Thermoplastic elastomers based upon chlorinated polyethylene and a crystalline olefin polymer

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