CA2470180A1 - Polyethylene melt blends for high density polyethylene applications - Google Patents
Polyethylene melt blends for high density polyethylene applications Download PDFInfo
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- CA2470180A1 CA2470180A1 CA002470180A CA2470180A CA2470180A1 CA 2470180 A1 CA2470180 A1 CA 2470180A1 CA 002470180 A CA002470180 A CA 002470180A CA 2470180 A CA2470180 A CA 2470180A CA 2470180 A1 CA2470180 A1 CA 2470180A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31938—Polymer of monoethylenically unsaturated hydrocarbon
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- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
Abstract
A polyethylene composition is provided that has a density of about 0.945 to about 0.960 g/cm3 and a melt flow index of about 0.1 to about 0.4. The composition is a melt blend of a linear low density polyethylene resin and/or a linear medium low density polyethylene resin, and a high density polyethylene resin. A feature of the composition is that the resins can independently be virgin, recycled, scrap and/or wide specification resins, and mixtures of these. Methods of producing the compositions and extruded, molded and formed plastic articles manufactured from the compositions are presented.
Description
POLYETHYLENE MELT BLENDS FOR HIGH DENSITY
POLYETHYLENE APPLICATIONS
BACKGROUND OF THE INVENTION
Plastic pipe, especially for use in drainage, irrigation, storm sewer and sanitary sewer applications, is produced from high density polyethylene (HDPE).
A typical pipe composition contains a high density polyethylene copolymer having a melt flow rate of approximately 0.15 to 0.4 grams per I O minutes that is blended with carbon black to minimize the effect of ultraviolet light. The Departments of Transportation (DOT) of many states of the United States require plastic pipe used for DOT projects to meet American Association of State Highway Transportation Officials (AASHTO) standards, that include American Society of Testing Materials (ASTM) standards. Current AASHTO standards for corrugated and profile HDPE pipe require the composition of the pipe to have the following properties: a minimum carbon black content of 2 percent by weight; a density of 0.945 to 0.955 grains per cubic centimeter (g/cm3); a melt flow index (MFI) maximum of 0.4; a minimum flexural modulus of 110,000 pounds per square inch (psi); a minimum tensile strength of 3,000 psi; and a minimum stress crack resistance of 24 hours determined by a notched constant tensile load test (NCTL) performed according to ASTM D5397. As used herein, the melt flow index is intended as an equivalent expression to the melt flow rate expressed as grams per 10 minutes at 190°C.
Many commercially available HDPE resins meeting the standards for density, MFI, flexural modulus and tensile strength, fail the NCTL test due to their characteristic broad molecular weight distribution (MWD) that includes the presence of a low molecular weight fraction that contributes to failure of the NCTL test.
To address this problem, specialized narrow MWD, stress crack resistant grades of HDPE have been produced by multistage polymerization to produce a bimodal or multimodal HDPE that when mixed with, for example, about 2 to about 6 percent by weight of carbon black, satisfies AASHTO requirements for corrugated and profile pipe. However, the reactor yield of the specialized HDPE
during polymerization typically varies directly with the breadth of the molecular weight distribution. As a result, HDPE resins with narrow MWD are usually sold at a premium.
In another approach, blending of polyethylene resins has been used to address the problem of stress crack resistance. For example, medium density polyethylene pipe blends with improved low temperature brittleness properties and gloss have been obtained, that are composed of HDPE and a concentrate mixture of linear low density polyethylene (LLDPE) and a carbon blaclc, where the LLDPE is a carrier for the carbon blaclc. This approach has the disadvantage that the resulting medium density polyethylene pipe blends have densities (e.g., 0.926 to 0.940 g/cm3) that are too low to meet the AASHTO requirements for corrugated and profile HDPE pipe. Other approaches employ two-stage HDPE
polymerization processes to produce bimodal HDPE that is used as a blending component for a resulting medium density polyethylene having a density of 0.930 to 0.940 g/cm3. Similarly, triblends containing a major portion of LLDPE and minor amounts of HDPEs of low molecular weight or high molecular weight have also been reported. However, none of the above methods results in an HDPE having a density of 0.945 to 0.955 g/cm3 and a MFI maximum of 0.4, required by AASHTO for corrugated and profile pipe.
SUMMARY OF THE INVENTION
The invention provides a melt-blended polyethylene composition that, when used in the manufacture of profile and corrugated pipe, pipe fittings, and the life, results in products that meet or exceed AASHTO standards for density, MFI, flexural modulus, tensile strength and stress crack resistance. An advantage of using a melt blended polyethylene composition in accordance with the invention is that, instead of the need for specially polymerized, premium cost HDPE for pipe, commodity grade resins, including virgin, recycled, scrap and wide specification resins, and the life, can be employed, resulting in significant cost savings. Moreover, by taking advantage of the properties of polyethylenes, especially density and melt flow index, molecular weight distribution, modality (i.e., unimodal, bimodal, or multimodal), and the like, HDPE can be selectively combined with LLDPE and/or linear medium density polyethylene (LMDPE) in a melt blend to result in compositions having the desired properties.
Thus, regardless of the combination of resins employed, the resulting melt blended polyethylene composition has a density of about 0.945 to about 0.960 g/cm3, preferably about 0.945 to about 0.955 g/cm3 and, especially, 0.945 to 0.955 g/cm3, a melt flow index of about 0.1 to about 0.4, preferably about 0.1 to 0.4, and a stress crack resistance of at least 24 hours. As used herein, (i) the density of the composition refers to the density prior to compounding of the composition with other materials, such as carbon black, and the like, and (ii) the term "polyethylene" shall admit of (though not require) the presence of small amounts of propylene, butene, hexene, octene and/or metallacene, and the lilce, as is lmown to those skilled in the art.
In one embodiment of the invention, the polyethylene composition comprises a melt blend of HDPE and at least one resin selected from the group consisting of LLDPE, LMDPE, and mixtures of these, the resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress craclc resistance of at least 24 hours. In a preferred embodiment, the HDPE can be present in an amount of about 50 to about 95 percent by weight. Correspondingly, the LLDPE and/or LMDPE can be present in an amount of about 5 to about 50 percent by weight.
The LLDPE and/or LMDPE preferably have a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3. The HDPE
preferably has a melt flow index of about 0.01 to about 1.5 and a density of about 0.941 to about 0.970 g/cm3.
In an embodiment of the invention, the HDPE can be selected from the group consisting of a high molecular weight high density polyethylene resin (HMW-HDPE) having a melt flow index of about 0.01 to about 0.2, a homopolymer high density polyethylene resin (H-HDPE) having a melt flow index of about 0.1 to about 1.5, and mixtures of these. The HMW-HDPE can have a density of about 0.941 to about 0.958 g/cm3, preferably about 0.945 to about 0.955 g/cm3. The H-HDPE can have a density of about 0.957 to about 0.970 g/cm3, preferably about 0.959 to about 0.965 g/cm3.
In the foregoing embodiments, the resins can be independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
The invention also provides methods for producing the melt blended polyethylene compositions according to embodiments of the invention, and extruded, molded or formed products, especially pipes and/or pipe fittings, comprising the composition.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure I illustrates a molecular weight distribution (MWD) curve for a typical prior art HDPE copolymer pipe resin having a low molecular weight tail.
Figure 2 illustrates a MWD curve for a prior art polymerized bimodal narrow molecular weight distribution HDPE copolymer overlaid with the curve of Figure 1.
Figure 3 illustrates component MWD curves for a blend of linear low density polyethylene (LLDPE) and a homopolymer high density polyethylene (H-HDPE), according to an embodiment of the invention, overlaid with the curve of Figure 1.
Figure 4 illustrates the resulting MWD curve for the melt blend of LLDPE and H- HDPE illustrated in Fig. 3, overlaid with the curve of Figure 1.
Figure 5 illustrates component MWD curves for a blend of LLDPE and a HMW-HDPE, according to an embodiment of the invention, overlaid with the curve of Figure 1.
Figure 6 illustrates the resulting MWD curve for the melt blend of LLDPE and HMW-HDPE illustrated in Fig. 5, overlaid with the curve of Figure 1.
Figure 7 illustrates component MWD curves for a terblend of LLDPE, H-HDPE and HMW-HDPE, according to an embodiment of the invention.
Figure 8 illustrates the resulting MWD curve for the melt blend of LLDPE, H-HDPE and HMW-HDPE illustrated in Fig. 7, overlaid with the curve of Figure 1.
DETAILED DESCRIPTION OF THE INVENTION
POLYETHYLENE APPLICATIONS
BACKGROUND OF THE INVENTION
Plastic pipe, especially for use in drainage, irrigation, storm sewer and sanitary sewer applications, is produced from high density polyethylene (HDPE).
A typical pipe composition contains a high density polyethylene copolymer having a melt flow rate of approximately 0.15 to 0.4 grams per I O minutes that is blended with carbon black to minimize the effect of ultraviolet light. The Departments of Transportation (DOT) of many states of the United States require plastic pipe used for DOT projects to meet American Association of State Highway Transportation Officials (AASHTO) standards, that include American Society of Testing Materials (ASTM) standards. Current AASHTO standards for corrugated and profile HDPE pipe require the composition of the pipe to have the following properties: a minimum carbon black content of 2 percent by weight; a density of 0.945 to 0.955 grains per cubic centimeter (g/cm3); a melt flow index (MFI) maximum of 0.4; a minimum flexural modulus of 110,000 pounds per square inch (psi); a minimum tensile strength of 3,000 psi; and a minimum stress crack resistance of 24 hours determined by a notched constant tensile load test (NCTL) performed according to ASTM D5397. As used herein, the melt flow index is intended as an equivalent expression to the melt flow rate expressed as grams per 10 minutes at 190°C.
Many commercially available HDPE resins meeting the standards for density, MFI, flexural modulus and tensile strength, fail the NCTL test due to their characteristic broad molecular weight distribution (MWD) that includes the presence of a low molecular weight fraction that contributes to failure of the NCTL test.
To address this problem, specialized narrow MWD, stress crack resistant grades of HDPE have been produced by multistage polymerization to produce a bimodal or multimodal HDPE that when mixed with, for example, about 2 to about 6 percent by weight of carbon black, satisfies AASHTO requirements for corrugated and profile pipe. However, the reactor yield of the specialized HDPE
during polymerization typically varies directly with the breadth of the molecular weight distribution. As a result, HDPE resins with narrow MWD are usually sold at a premium.
In another approach, blending of polyethylene resins has been used to address the problem of stress crack resistance. For example, medium density polyethylene pipe blends with improved low temperature brittleness properties and gloss have been obtained, that are composed of HDPE and a concentrate mixture of linear low density polyethylene (LLDPE) and a carbon blaclc, where the LLDPE is a carrier for the carbon blaclc. This approach has the disadvantage that the resulting medium density polyethylene pipe blends have densities (e.g., 0.926 to 0.940 g/cm3) that are too low to meet the AASHTO requirements for corrugated and profile HDPE pipe. Other approaches employ two-stage HDPE
polymerization processes to produce bimodal HDPE that is used as a blending component for a resulting medium density polyethylene having a density of 0.930 to 0.940 g/cm3. Similarly, triblends containing a major portion of LLDPE and minor amounts of HDPEs of low molecular weight or high molecular weight have also been reported. However, none of the above methods results in an HDPE having a density of 0.945 to 0.955 g/cm3 and a MFI maximum of 0.4, required by AASHTO for corrugated and profile pipe.
SUMMARY OF THE INVENTION
The invention provides a melt-blended polyethylene composition that, when used in the manufacture of profile and corrugated pipe, pipe fittings, and the life, results in products that meet or exceed AASHTO standards for density, MFI, flexural modulus, tensile strength and stress crack resistance. An advantage of using a melt blended polyethylene composition in accordance with the invention is that, instead of the need for specially polymerized, premium cost HDPE for pipe, commodity grade resins, including virgin, recycled, scrap and wide specification resins, and the life, can be employed, resulting in significant cost savings. Moreover, by taking advantage of the properties of polyethylenes, especially density and melt flow index, molecular weight distribution, modality (i.e., unimodal, bimodal, or multimodal), and the like, HDPE can be selectively combined with LLDPE and/or linear medium density polyethylene (LMDPE) in a melt blend to result in compositions having the desired properties.
Thus, regardless of the combination of resins employed, the resulting melt blended polyethylene composition has a density of about 0.945 to about 0.960 g/cm3, preferably about 0.945 to about 0.955 g/cm3 and, especially, 0.945 to 0.955 g/cm3, a melt flow index of about 0.1 to about 0.4, preferably about 0.1 to 0.4, and a stress crack resistance of at least 24 hours. As used herein, (i) the density of the composition refers to the density prior to compounding of the composition with other materials, such as carbon black, and the like, and (ii) the term "polyethylene" shall admit of (though not require) the presence of small amounts of propylene, butene, hexene, octene and/or metallacene, and the lilce, as is lmown to those skilled in the art.
In one embodiment of the invention, the polyethylene composition comprises a melt blend of HDPE and at least one resin selected from the group consisting of LLDPE, LMDPE, and mixtures of these, the resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress craclc resistance of at least 24 hours. In a preferred embodiment, the HDPE can be present in an amount of about 50 to about 95 percent by weight. Correspondingly, the LLDPE and/or LMDPE can be present in an amount of about 5 to about 50 percent by weight.
The LLDPE and/or LMDPE preferably have a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3. The HDPE
preferably has a melt flow index of about 0.01 to about 1.5 and a density of about 0.941 to about 0.970 g/cm3.
In an embodiment of the invention, the HDPE can be selected from the group consisting of a high molecular weight high density polyethylene resin (HMW-HDPE) having a melt flow index of about 0.01 to about 0.2, a homopolymer high density polyethylene resin (H-HDPE) having a melt flow index of about 0.1 to about 1.5, and mixtures of these. The HMW-HDPE can have a density of about 0.941 to about 0.958 g/cm3, preferably about 0.945 to about 0.955 g/cm3. The H-HDPE can have a density of about 0.957 to about 0.970 g/cm3, preferably about 0.959 to about 0.965 g/cm3.
In the foregoing embodiments, the resins can be independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
The invention also provides methods for producing the melt blended polyethylene compositions according to embodiments of the invention, and extruded, molded or formed products, especially pipes and/or pipe fittings, comprising the composition.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure I illustrates a molecular weight distribution (MWD) curve for a typical prior art HDPE copolymer pipe resin having a low molecular weight tail.
Figure 2 illustrates a MWD curve for a prior art polymerized bimodal narrow molecular weight distribution HDPE copolymer overlaid with the curve of Figure 1.
Figure 3 illustrates component MWD curves for a blend of linear low density polyethylene (LLDPE) and a homopolymer high density polyethylene (H-HDPE), according to an embodiment of the invention, overlaid with the curve of Figure 1.
Figure 4 illustrates the resulting MWD curve for the melt blend of LLDPE and H- HDPE illustrated in Fig. 3, overlaid with the curve of Figure 1.
Figure 5 illustrates component MWD curves for a blend of LLDPE and a HMW-HDPE, according to an embodiment of the invention, overlaid with the curve of Figure 1.
Figure 6 illustrates the resulting MWD curve for the melt blend of LLDPE and HMW-HDPE illustrated in Fig. 5, overlaid with the curve of Figure 1.
Figure 7 illustrates component MWD curves for a terblend of LLDPE, H-HDPE and HMW-HDPE, according to an embodiment of the invention.
Figure 8 illustrates the resulting MWD curve for the melt blend of LLDPE, H-HDPE and HMW-HDPE illustrated in Fig. 7, overlaid with the curve of Figure 1.
DETAILED DESCRIPTION OF THE INVENTION
5 A polyethylene composition in accordance with the invention is a melt blend of high density polyethylene resins especially for use in the manufacture of pipe and pipe fittings, such as, but not limited to, those used for drainage, irngation, storm sewer and sanitary sewer applications. The composition is particularly useful for extruded, injection molded and blow molded profile and corrugated pipe and pipe fittings. The composition is also useful in the manufacture of other extruded, molded or formed plastic articles such as, but not limited to, smooth or corrugated conduit pipe for electrical, fiber-optic and telecommunication applications, wire and cable insulation materials, injection molded parts, extruded films and sheets (e.g., geomembranes and environmental films, such as those used for pond liners, landfill liners, and the life), environmental chambers, and the like, especially for applications in which good stress crack resistance is desired.
As referred to herein, density, MFI and stress cracf resistance measurements are obtained according to ASTM D1505, ASTM D1238, and ASTM D5397, respectively. Flexural modulus and tensile strength are measurea according to ASTM D790 and ASTM D638, respectively. Other tests that may be conducted for stress cracf resistance include, but are not limited to, the standard bent strip Environmental Stress Craclc Resistance test (ESCR), according to ASTM D1693, the Notched Constant Ligament Stress Test (ASTM
D5397), and the Bottle ESCR test (ASTM D2561).
Enhancement of the environmental and long term stress cracf resistance of polyethylene molded articles is dependent on increasing the number of tie molecules connecting the crystalline lamellae of the semicrystalline high density polyethylene material. The number of tie molecules is inversely related to the low molecular weight faction of the polyethylene that forms the molded article.
In other words, the low molecular weight polyethylene molecules associated with broad molecular weight distribution HDPE diminish the number of tie molecules between lamellae, with the effect of decreasing the stress crack resistance.
Until the present invention, pipe manufacturers have had to rely on specially polymerized and expensive HDPE to satisfy standards for the physical properties of pipe. Conventional commodity HDPE has been unsatisfactory for use because of its broad molecular weight distribution, which includes a low molecular weight tail that contributes to failure of the NCTL test for stress crack resistance over a 24 hour period.
To address this problem, one embodiment of the invention provides a polyethylene composition in which LLDPE and/or LMDPE, and HDPE are melt blended together, for example in an extruder or other mixer (e.g., Banbury, Henschel, and the Iike), in amounts relative to one another such that the resulting melt-blended, moldable or otherwise formable polyethylene composition has a density of about 0.945 to about 0.960 g/cm3, preferably about 0.945 to about 0.955 g/cm3, a MFI of about 0.1 to about 0.4, preferably about 0.1 to 0.4, and a stress crack resistance of at least 24 hours. Preferably, the HDPE resin is present in the composition in an amount of about 50 to about 95 percent by weight and, correspondingly, the LLDPE and/or the LMDPE is present in an amount of about 5 to about 50 percent by weight.
Figure 1 illustrates the broad shape of the MWD of a conventional HDPE
copolymer pipe resin (10) including the low molecular weight tail. A MWD
curve for a specially polymerized bimodal narrow MWD HDPE copolymer (20) having a MFI in the same range as that of HDPE (10) is illustrated in Figure 2, with the curve of Figure 1 (dotted line) superimposed for comparison. The specialty HDPE (20) has superior stress crack resistance because it does not contain the low molecular weight tail present in conventional HDPE (10). The specialty HDPE (20) also has good processing characteristics based on its bimodal MWD.
A narrow MWD (i.e., the absence of a low molecular weight tail) is also characteristic of polymerized LLDPE and LMDPE resins. Because of this narrow MWD, LLDPE and LMDPE have a high stress crack resistance.
However LLDPE and LMDPE have a high melt flow rate (MFI), which can malce processing difficult during extrusion and molding applications. The invention takes advantage of the high stress crack resistance characteristic of LLDPE
and/or LMDPE, by melt blending LLDPE and/or LMDPE having a density of about 0.920 to about 0.940 g/cm3 with a higher density conventional homopolymer HDPE (H-HDPE) or high molecular weight HDPE (HMW-HDPE) to increase processability. As the average molecular weight of the HDPE
employed in the composition is increased, the more the MWD of the composition shifts to higher molecular weight. For example, an LLDPE and/or LMDPE
having a density of about 0.920 to about 0.940 g/cm3 can be melt blended with a H-HDPE having a density greater than 0.959 g/cm3, to lift the blended density into the preferred density range of about 0.945 to about 0.960 g/cm3. The MWD
curves of the individual blend components of LLDPE (30) and a unimodal H-HDPE (40), of a composition according to the invention are illustrated in Figure 3. The resulting bimodal MWD curve (50) of the melt blend containing these components is illustrated in Figure 4. The curve of the conventional HDPE
resin (10) (dotted line) from Figure 1 is superimposed on each of the curves, for comparison. As illustrated in Figure 4, the low molecular weight tail of the resulting melt blend compositions is greatly reduced compared to the low molecular weight tail of the conventional HDPE resin.
Figure 5 illustrates the individual MWD curves of a melt blend composition according to the invention containing LLDPE (30) and a unimodal HMW-HDPE (60). As used in the context of the melt blended polyethylene compositions according to the invention, a HMW-HDPE is one that has a sufficiently high molecular weight that it, by itself, has a NCTL stress crack resistance that exceeds 24 hours. The HMW-HDPE (60) employed in the compositions also has a molecular weight that is sufficiently high that it does not contribute molecules of lower molecular weight than those of the LLDPE (30).
Figure 6 illustrates the bimodal MWD curve (70) of the resulting polyethylene melt blend, with the curve of the conventional HDPE resin (10) (dotted line) from Figure 1 superimposed for comparison. In comparison with the conventional HDPE resin, the low molecular weight tail in this embodiment of the invention melt blend has disappeared.
As referred to herein, density, MFI and stress cracf resistance measurements are obtained according to ASTM D1505, ASTM D1238, and ASTM D5397, respectively. Flexural modulus and tensile strength are measurea according to ASTM D790 and ASTM D638, respectively. Other tests that may be conducted for stress cracf resistance include, but are not limited to, the standard bent strip Environmental Stress Craclc Resistance test (ESCR), according to ASTM D1693, the Notched Constant Ligament Stress Test (ASTM
D5397), and the Bottle ESCR test (ASTM D2561).
Enhancement of the environmental and long term stress cracf resistance of polyethylene molded articles is dependent on increasing the number of tie molecules connecting the crystalline lamellae of the semicrystalline high density polyethylene material. The number of tie molecules is inversely related to the low molecular weight faction of the polyethylene that forms the molded article.
In other words, the low molecular weight polyethylene molecules associated with broad molecular weight distribution HDPE diminish the number of tie molecules between lamellae, with the effect of decreasing the stress crack resistance.
Until the present invention, pipe manufacturers have had to rely on specially polymerized and expensive HDPE to satisfy standards for the physical properties of pipe. Conventional commodity HDPE has been unsatisfactory for use because of its broad molecular weight distribution, which includes a low molecular weight tail that contributes to failure of the NCTL test for stress crack resistance over a 24 hour period.
To address this problem, one embodiment of the invention provides a polyethylene composition in which LLDPE and/or LMDPE, and HDPE are melt blended together, for example in an extruder or other mixer (e.g., Banbury, Henschel, and the Iike), in amounts relative to one another such that the resulting melt-blended, moldable or otherwise formable polyethylene composition has a density of about 0.945 to about 0.960 g/cm3, preferably about 0.945 to about 0.955 g/cm3, a MFI of about 0.1 to about 0.4, preferably about 0.1 to 0.4, and a stress crack resistance of at least 24 hours. Preferably, the HDPE resin is present in the composition in an amount of about 50 to about 95 percent by weight and, correspondingly, the LLDPE and/or the LMDPE is present in an amount of about 5 to about 50 percent by weight.
Figure 1 illustrates the broad shape of the MWD of a conventional HDPE
copolymer pipe resin (10) including the low molecular weight tail. A MWD
curve for a specially polymerized bimodal narrow MWD HDPE copolymer (20) having a MFI in the same range as that of HDPE (10) is illustrated in Figure 2, with the curve of Figure 1 (dotted line) superimposed for comparison. The specialty HDPE (20) has superior stress crack resistance because it does not contain the low molecular weight tail present in conventional HDPE (10). The specialty HDPE (20) also has good processing characteristics based on its bimodal MWD.
A narrow MWD (i.e., the absence of a low molecular weight tail) is also characteristic of polymerized LLDPE and LMDPE resins. Because of this narrow MWD, LLDPE and LMDPE have a high stress crack resistance.
However LLDPE and LMDPE have a high melt flow rate (MFI), which can malce processing difficult during extrusion and molding applications. The invention takes advantage of the high stress crack resistance characteristic of LLDPE
and/or LMDPE, by melt blending LLDPE and/or LMDPE having a density of about 0.920 to about 0.940 g/cm3 with a higher density conventional homopolymer HDPE (H-HDPE) or high molecular weight HDPE (HMW-HDPE) to increase processability. As the average molecular weight of the HDPE
employed in the composition is increased, the more the MWD of the composition shifts to higher molecular weight. For example, an LLDPE and/or LMDPE
having a density of about 0.920 to about 0.940 g/cm3 can be melt blended with a H-HDPE having a density greater than 0.959 g/cm3, to lift the blended density into the preferred density range of about 0.945 to about 0.960 g/cm3. The MWD
curves of the individual blend components of LLDPE (30) and a unimodal H-HDPE (40), of a composition according to the invention are illustrated in Figure 3. The resulting bimodal MWD curve (50) of the melt blend containing these components is illustrated in Figure 4. The curve of the conventional HDPE
resin (10) (dotted line) from Figure 1 is superimposed on each of the curves, for comparison. As illustrated in Figure 4, the low molecular weight tail of the resulting melt blend compositions is greatly reduced compared to the low molecular weight tail of the conventional HDPE resin.
Figure 5 illustrates the individual MWD curves of a melt blend composition according to the invention containing LLDPE (30) and a unimodal HMW-HDPE (60). As used in the context of the melt blended polyethylene compositions according to the invention, a HMW-HDPE is one that has a sufficiently high molecular weight that it, by itself, has a NCTL stress crack resistance that exceeds 24 hours. The HMW-HDPE (60) employed in the compositions also has a molecular weight that is sufficiently high that it does not contribute molecules of lower molecular weight than those of the LLDPE (30).
Figure 6 illustrates the bimodal MWD curve (70) of the resulting polyethylene melt blend, with the curve of the conventional HDPE resin (10) (dotted line) from Figure 1 superimposed for comparison. In comparison with the conventional HDPE resin, the low molecular weight tail in this embodiment of the invention melt blend has disappeared.
In a preferred embodiment of the invention illustrated in Figure 7, the LLDPE (30) is melt blended with both a unimodal H-HDPE (40) and a HMW-HDPE (60) to produce the trimodal MWD curve illustrated in Figure 8. In comparison with the conventional HDPE resin, the low molecular weight tail in this embodiment of the melt blend is greatly reduced.
Another property that contributes to the selection of resins for the melt blend compositions according to the invention is the melt flow index, which is a measure of the viscosity of the component and affects the processability of the melt blend. For example, LLDPE having a high MFI can be melt blended with a HDPE having a lower MFI to achieve the desired stiffness and, therefore, the desired processability. The melt flow index is a general indicator of the weight average molecular weight of the resins.
Yet another property that contributes to the selection of resins for the melt blend compositions of the invention is the Flow Rate Ratio (FRR), such as that defined in ASTM D1238, which is a good indicator of the weight average molecular weight and a generally accepted test method for the polydispersity of polyethylene resin grades. Polydispersity is the ratio of the weight average molecular weight to the number average molecular weight, and the lower the polydispersity (and the FRR), the narrower is the MWD. Polydispersity can be measured by gel permeation chromatography (GPC), although this is not generally recommended for polyethylene resins, which have poor solubility unless special solvents are employed. GPC is also difficult to conduct as a quality control test on, for example, recycled and/or scrap resin products for use in the invention compositions. For example, such recycled or scrap products may include, but are not limited to, such usuable resins obtained as "mills jugs"
produced from H-HDPE, "T-shirt bags" constructed from bimodal HMW-HDPE, recycled 55 gallon drums constructed from HMW-HDPE, plastic dry cleaning bag material made of LLDPE, and the lilce. Because it is a simple test to conduct, the FRR is, therefore, preferred to GPC for estimating the polydispersity of the resins, where the polydispersity is not specified, prior to their use in the melt blend compositions.
Another property that contributes to the selection of resins for the melt blend compositions according to the invention is the melt flow index, which is a measure of the viscosity of the component and affects the processability of the melt blend. For example, LLDPE having a high MFI can be melt blended with a HDPE having a lower MFI to achieve the desired stiffness and, therefore, the desired processability. The melt flow index is a general indicator of the weight average molecular weight of the resins.
Yet another property that contributes to the selection of resins for the melt blend compositions of the invention is the Flow Rate Ratio (FRR), such as that defined in ASTM D1238, which is a good indicator of the weight average molecular weight and a generally accepted test method for the polydispersity of polyethylene resin grades. Polydispersity is the ratio of the weight average molecular weight to the number average molecular weight, and the lower the polydispersity (and the FRR), the narrower is the MWD. Polydispersity can be measured by gel permeation chromatography (GPC), although this is not generally recommended for polyethylene resins, which have poor solubility unless special solvents are employed. GPC is also difficult to conduct as a quality control test on, for example, recycled and/or scrap resin products for use in the invention compositions. For example, such recycled or scrap products may include, but are not limited to, such usuable resins obtained as "mills jugs"
produced from H-HDPE, "T-shirt bags" constructed from bimodal HMW-HDPE, recycled 55 gallon drums constructed from HMW-HDPE, plastic dry cleaning bag material made of LLDPE, and the lilce. Because it is a simple test to conduct, the FRR is, therefore, preferred to GPC for estimating the polydispersity of the resins, where the polydispersity is not specified, prior to their use in the melt blend compositions.
The FRR is the ratio of the high load melt index (HLMI, condition F at 21.6 lcg at 190°C) to the melt index (MI, condition E at 2.16 kg and 190°C). For example, an LLDPE or a LMDPE with a nominal MI of 0.7 and a HLMI of 21.0 would have an FRR (HLMI/MI = 21.0/0.7) of about 30. HMW-HDPE having an HLMI of 4.5 and an MI of 0.05 would have an FRR of about 90. Both of these materials would be considered to have a nanow molecular weight distribution and low polydispersity. Polyethylene resins suitable for use in the invention compositions can have a FRR of about 20 to about 200, preferably about 90 to about 130. The LLDPE and LMDPE resins suitable for use in the compositions according to the invention have a very narrow MWD and an FRR of about 20 to about 60.
The FRR is also a good indicator of the processability at higher shear rates of the final melt blended compound. Therefore, an advantage of the methods of the invention, is that the FRR of a final composition can be predetermined by selecting resins having FRR values that will achieve desired processing and final product considerations, such as processability, melt strength, die swell ratio, forming, wall thickness, and the like. It is preferred that the final melt-blended composition have an FRR of about 80 to about 130, with about 90 to about 110 being more preferred. It has been found that melt-blended compositions with FRR greater than 150 risk failing the 24 hour stress crack resistance test (NCTL) and may be difficult to process.
The LLDPE, LMDPE and HDPE resins used in the composition, methods, and articles according to the invention, can be unimodal, bimodal, multimodal, or mixtures of these types. By the "modality" of the resins, is meant the number of peaks in a molecular weight distribution curve.
In one embodiment of the invention, a polyethylene composition comprises a melt blend of HDPE and at least one resin selected from the group consisting of LLDPE, LMDPE, and mixtures thereof, the resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours. The resins axe independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
The LLDPE and/or the LMDPE can be present in the composition in an amount of about 5 to about 50 percent by weight, preferably about 15 to about 45 percent by weight and, more preferably, about 20 to about 35 percent by weight. The 5 LLDPE and/or the LMDPE resin can have a melt flow index of about 0.1 to about 1.5, preferably about 0.4 to about 1Ø The density of the linear resins can range from about 0.920 to about 0.940 g/cm3, preferably about 0.925 to about 0.935 g/cm3. As lcnov~m to those spilled in the art, the density of LLDPE is about 0.910 to 0.925 g/cm3, and the density of LMDPE is about 0.926 to about 0.940 10 glcm3. However, suitable LLDPE for use in the compositions according to the invention has a density of about 0.920 to about 0.925 g/cm3.
The HDPE resin can be selected from the group consisting of HMW-HDPE resin having a melt flow index of about 0.01 to about 0.2, preferably about 0.05 to about 0.15, and H-HDPE having a melt flow index of about 0.1 to about 1.5, preferably about 0.3 to about 1.0, and mixtures thereof. The HMW-HDPE
can have a density of about 0.941 to about 0.958 g/cm3, preferably about 0.945 to about 0.955 g/cm3 and the H-HDPE can have a density of about 0.957 to about 0.970 g/cm3, preferably about 0.959 to about 0.965 g/cm3. The HDPE
component can be present in the composition in an amount of about 50 to about 95 percent by weight, preferably about 55 to about 85 percent by weight. The H-HDPE can be present in an amount of about 50 to about 95 percent by weight.
More preferably, the H-HDPE is present in an amount of about 55 to about 85 percent by weight.
A suitable HMW-HDPE for use in the melt blends according to the invention has a weight average molecular weight of about 100,000 to about 1,000,000 daltons. As is lmown to those slcilled in the art, the melt flow index of the polymer varies inversely with the molecular weight. According to the invention, the HMW-HDPE is preferably selected based on its melt flow index and density, rather than its particular molecular weight.
Any or all of the LLDPE and/or the LMDPE and the HDPE resins in the embodiments of the invention melt blended compositions can be recycled, wide specification, scrap and/or virgin resin, with mixtures of these source resins being typical. In particular, the use of recycled, wide specification and/or scrap resins is very economical in comparison to the use of virgin resins. Suitable virgin, scrap, recycled and wide specification LLDPE, H-HDPE, and HMW-HDPE are l~nown in the art. Virgin resins are commercially available from, for example, Exxon Mobil Corporation (Irving, TX), Chevron Phillips Chemical Company LP
(Houston, TX), Dow Chemical Company (Midland, MI), Ipiranga Quimica (Porto Alegre, Brazil), Samsung General Chemicals Co., Ltd. (Seosan, Korea), and SABIC Plastic Products (Riyadh, Saudi Arabia).
Exemplary recycled and/or scrap LLDPE and LMDPE can be, but are not limited to, for example, printed plastic dry cleaning bag material, off color plastic bags and the lilce. The visual characteristics of the printed or off color plastic bags are not apparent when used in compositions for applications, including pipe and pipe fittings, where the addition of carbon black or another colorant masl~s the off color material and/or the printing dye. Exemplary recycled and/or scrap HMW-HDPE film used to make plastic bags, such as grocery bags or "T-shirt bags" for the retail clothing industry, and the life, rnay be recycled for use in the melt blends in accordance with the invention. For example, such plastic bags can be constructed of bimodal HMW-HDPE. Other examples of recyclable materials constructed of HMW-HDPE include, but are not limited to, 55 gallon plastic drums. H-HDPE used to male mills jugs or other such containers, for example, may be recycled for use in the melt blends in accordance with the invention.
Wide specification resins differ from on-specification resins in that a wide specification resin is out of the desired specification range for at least one physical property including, but not limited to, density, melt flow index and FRR.
Because on-specification resins are desirable and sometimes necessary for particular applications, they can command a premium price. Therefore, by using wide specification resins in the melt blends of the embodiments of the invention composition, it is possible to achieve a cost savings in comparison to using resins having specified properties. As a non-limiting example, when wide specification LLDPE and/or LMDPE resin is employed, the physical properties of the melt blend compositions are obtained by compensating for the out-of range specification characteristic with a formulation change that can include one or more HDPEs having a corresponding off setting characteristic. For example, to compensate for LLDPE having a melt flow index in a range of 0.4 to 1.0, HDPE
having a low melt flow index of, for example, 0.01 to 0.1 can be employed, or the proportion of HDPE with a melt flow index range of, for example, 0.05 to 0.1 can be increased in the composition. As another example, to compensate for LLDPE
having a density of, for example, 0.920 g/cm3, a 50:50 mixture of the LLDPE
and an H-HDPE having a density of 0.965 g/cm3 can be employed, to bring the density of the final product to 0.945 g/cm3. However, because LLDPE has good stress crack resistance, it is desirable to use a only small amount of, for example, H-HDPE which has a low stress cracl~ resistance. In general, as the density of the HDPE increases, the less is the amount of the HDPE required in the composition to achieve the desired density, melt flow index and other physical properties.
A feature of the invention compositions is that more than one LLDPE, LMDPE, H-HDPE, and/or HMW-HDPE, each b.aving individual ranges of density, MFI and/or FRR and/or modalities, can be employed to increase the flexibility by which components can be melt-blended together in order to achieve the desired physical characteristics of the resulting composition. For example, it is possible to use combinations of resins that include, for example but not limited to, one to about 6 or more individual LLDPEs, LMDPEs, H-HDPEs, and/or HMW-HDPEs.
Once in possession of the teachings herein, including the examples below, of cornponents which can be utilized to achieve the desired physical properties of the melt blend compositions, the selection of suitable components, not limited to those expressly disclosed, will be within the ordinary shill in the art. The invention practitioner will be able to adjust the components of the composition for specification variations without undue experimentation.
The melt-blended compositions of the invention can be used to produce an extruded, molded or formed plastic article having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress cracl~
resistance of at least 24 hours. Exemplary articles include, but are not limited to, pipe, including conduit pipe, pipe fittings, wire insulation material, cable insulation materials, films, sheets, and environmental chambers, especially for applications described above.
The melt-blended compositions of the invention are particularly useful to produce profile or corrugated pipe and/or pipe fittings, having physical properties that conform to applicable standards. As a non-limiting example of pipe and pipe fitting applications, the compositions can be used to produce profile and corrugated pipe having a density of 0.945 to 0.955, a MFI of about 0.1 to 0.4, a minimum flexural modulus of 110,000 psi, a minimum tensile strength of 3,000 psi and a minimum stress crack resistance of at least 24 hours, as required by current AASHTO standards.
Generally, a small diameter extruded pipe (e.g., about 2 inches to about 12 inches) is easier to extrude and form. Thus, a small diameter pipe, for example, can be formed from a melt blend composition of the invention having a MFI of about 0.3 to less than 0.4; whereas a large diameter extruded pipe (e.g., about 36 inches to about 72 inches) should be stiffer for extrusion and forming.
Therefore a large diameter pipe can be formed from a melt blend composition having a MFI of about 0.15 to about 0.2, for example. Medium diameter pipes (e.g., about 15 inches to about 30 inches) can be formed from a melt blend composition having a moderate MFI of about 0.2 to about 0.3, for example.
Similarly, it is generally understood that the processability of corrugated pipe is improved by an increased stiffness of the melt blend, in comparison to the stiffness of the melt blend used to produce profile pipe. Accordingly, one of ordinary slcill in the art could produce pipe according to the invention by varying the proportions of the melt blend components in the melt blend until the desired melt flow index and density of the composition was achieved, without undue experimentation.
Natural ethylene polymers have a detrimental property in that they slowly degrade in the presence of oxygen (air), and the degradation is l~nown to be accelerated by the presence of heat and/or ultraviolet radiation. Preferably, pipes or pipe fittings comprising the melt blended composition are compounded with small amounts of carbon blacl~, or other photo- and thermal-oxidation retarders to minimize the effects of heat and ultra violet light. For example, the composition can comprise carbon black (about 1 percent to about 5 percent, preferably about 2 percent to about 3 percent by weight). The carbon blacks can include any of the commonly available, commercially-produced carbon blacks including, but not limited to, furnace blacks, acetylene blacks, channel blacks and lamp blacks.
The compositions according to the invention may also comprise other additives customary for use in resin-based compositions, according to the application for which they are being used. Such additives include, but are not limited to, antioxidants, antiozonants, lubricants, stabilizers, processing aids, water-proofing fillers, inorganic fillers, colorants, curatives, and the like.
These additives are used in amounts designed to provide their intended effect in the resulting composition. The total amount of such additives can range from zero to about 10 percent by weight based on the total weight of the composition.
In one embodiment, a method for producing a polyethylene composition according to the invention comprises melt blending together a sufficient amount of a HDPE resin and a sufficient amount of at least one additional resin selected from the group consisting of LLDPE resins, LMDPE resins, and mixtures thereof, to produce a melt-blended composition having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours. The HDPE resin can be present in an amount of about 50 to about 95 percent by weight.
In another embodiment, a method for producing a polyethylene composition according to the invention comprises melt blending together a sufficient amount of a HDPE resin selected from the group consisting of a HMW-HDPE resin having a density of about 0.941 to about 0.958 g/cm3 and a melt flow index of about 0.01 to about 0.2, a H-HDPE resin having a density of about 0.957 to about 0.970 g/cm3 and a melt flow index of about 0.1 to about 1.5, and mixtures thereof; and a sufficient amount of at least one additional polyethylene resin having a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3, to produce a melt-blended composition having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress craclc resistance of at least 24 hours. The HDPE resin can be present in an amount of about 50 to about 95 percent by weight.
The LLDPE, LMDPE and HDPE resins can be in pellet, powdered, flake or regrind form, or the like. The methods are not intended to be limited to any one method of melt blending the components. For example, mixing or melt blending of components, including any additives if used, can be by batch 5 compounding, such as in a Banbury or Henschel type mixer, or can be continuous compounding in an extruder. For example, in one embodiment of the method, the components of the composition can be dry-blended prior to melt blending by single screw or twin screw extrusion. In another embodiment, the dry components can be separately fed through separate ports into an extruder for melt 10 blending. In yet another embodiment, the two or more components can be pre-combined in a mixer, such as a Banbury or Henschel mixer, preferably under high intensity blending, to form a hot melt which then can be combined with a third component (e.g., a let down resin) in an extruder. For example, a sufficient amount of LLDPE and H-HDPE can be preblended in a Banbury mixer, and the 15 resulting composition blended with a sufficient amount of HMW-HDPE in an extruder to produce the desired percentages of each of the three types of components in the final composition. Moreover, any of the components can be mixed with, for example, carbon black or other colorants and/or other additives, as a master batch, which is then added to a let down resin comprising one or more of the remaining components, to produce the desired percentages of the components in the final composition. As a non-limiting example, 25% of a master batch composition comprising 90% LLDPE and 10% carbon blaclc can be combined with 75% HDPE let down resin to provide the desired amount of LLDPE, HDPE and carbon black in the final composition to provide the desired properties of density and melt flow index. The temperatures and other variables required for dry blending, hot melts, and melt blending are well known to those skilled in the art.
Following melt blending of the components, the composition can be inj ection molded, blow molded, rolled, milled, sheet extruded, film extruded, pipe extruded, or formed or fabricated in any manner whatsoever to form the desired product by known methods. Once the teachings herein are in hand, the skilled practitioner of this invention will be able to adapt conventional methods of forming material, such as inj ection molding and other techniques mentioned above, to the production of desired articles of manufacture using the polyethylene composition of the invention. This adaptation can be implemented on an empirical basis, without undue experimentation.
S EXAMPLES
The following examples illustrate methods of preparation of melt blended polyethylene compositions of the invention. However, the examples are not intended to be limiting, as other methods for preparing these compounds and different compounding formulations may be determined by those spilled in the art. Further, the blend components are not limited to the specific polyethylenes shown. Thus, it is believed that any of the variables disclosed herein can readily be determined and controlled without departing from the scope of the invention herein disclosed and described.
Below are three examples of preferred embodiments in which the mix 1S ratios of LLDPE, H-HDPE and HMW-HDPE components differ with respect to each other. In each of the following examples, the exemplary polyethylene was _ prepared under industry standard conditions using melt blending techniques as known in the art. Dry mixtures of pelletized LLDPE and HDPEs were introduced directly into a profile extruder to produce HDPE pipe.
The H-HDPE used in all of the following examples was Grade GD 4960, supplied by Ipiranga Quimica (1'orto Alegre, Brazil), having a melt flow index of 0.80 and a density of 0.962 g/cm3. The HMW-HDPE used in all of the examples was grade F120A, supplied by Samsung General Chemicals Co., Ltd. (Seosan, Korea), having a melt flow index of 0.044 and a density of 0.956 g/cm3. The 2S LLDPE used in all of the examples was Grade 726N, supplied by SABIC Plastic Products (a division of Saudi Arabia Basic Industries Corporation, Riyadh, Saudi Arabia), having a melt flow index of 0.70 and a density of 0.926 g/cm3.
Example 1 The percentages by weight of the polyethylene components used to produce a melt-blended polyethylene composition suitable for a producing a pipe having a diameter of about 24 to about 30 inches are listed below. The physical properties of the resulting melt-blended polyethylene composition are illustrated in Table 1.
35% H-HDPE
20% HMW-HDPE
45% LLDPE
Example 2 The percentages by weight of the polyethylene components used to produce a melt-blended polyethylene composition suitable for a producing a pipe having a diameter of about 12 to about 1S inches are listed below. The physical properties of the resulting melt-blended polyethylene composition are illustrated in Table 1.
40% H-HDPE
40% HMW-HDPE
20% LLDPE
Example 3 The percentages by weight of the polyethylene components used to produce a melt-blended polyethylene composition suitable for a producing a pipe having a diameter of about 36 to about 72 inches are listed below. The physical properties of the resulting melt-blended polyethylene composition are illustrated in Table 1.
3 5 % H-HDPE
5 5 % HMW-HDPE
10% LLDPE
The FRR is also a good indicator of the processability at higher shear rates of the final melt blended compound. Therefore, an advantage of the methods of the invention, is that the FRR of a final composition can be predetermined by selecting resins having FRR values that will achieve desired processing and final product considerations, such as processability, melt strength, die swell ratio, forming, wall thickness, and the like. It is preferred that the final melt-blended composition have an FRR of about 80 to about 130, with about 90 to about 110 being more preferred. It has been found that melt-blended compositions with FRR greater than 150 risk failing the 24 hour stress crack resistance test (NCTL) and may be difficult to process.
The LLDPE, LMDPE and HDPE resins used in the composition, methods, and articles according to the invention, can be unimodal, bimodal, multimodal, or mixtures of these types. By the "modality" of the resins, is meant the number of peaks in a molecular weight distribution curve.
In one embodiment of the invention, a polyethylene composition comprises a melt blend of HDPE and at least one resin selected from the group consisting of LLDPE, LMDPE, and mixtures thereof, the resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours. The resins axe independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
The LLDPE and/or the LMDPE can be present in the composition in an amount of about 5 to about 50 percent by weight, preferably about 15 to about 45 percent by weight and, more preferably, about 20 to about 35 percent by weight. The 5 LLDPE and/or the LMDPE resin can have a melt flow index of about 0.1 to about 1.5, preferably about 0.4 to about 1Ø The density of the linear resins can range from about 0.920 to about 0.940 g/cm3, preferably about 0.925 to about 0.935 g/cm3. As lcnov~m to those spilled in the art, the density of LLDPE is about 0.910 to 0.925 g/cm3, and the density of LMDPE is about 0.926 to about 0.940 10 glcm3. However, suitable LLDPE for use in the compositions according to the invention has a density of about 0.920 to about 0.925 g/cm3.
The HDPE resin can be selected from the group consisting of HMW-HDPE resin having a melt flow index of about 0.01 to about 0.2, preferably about 0.05 to about 0.15, and H-HDPE having a melt flow index of about 0.1 to about 1.5, preferably about 0.3 to about 1.0, and mixtures thereof. The HMW-HDPE
can have a density of about 0.941 to about 0.958 g/cm3, preferably about 0.945 to about 0.955 g/cm3 and the H-HDPE can have a density of about 0.957 to about 0.970 g/cm3, preferably about 0.959 to about 0.965 g/cm3. The HDPE
component can be present in the composition in an amount of about 50 to about 95 percent by weight, preferably about 55 to about 85 percent by weight. The H-HDPE can be present in an amount of about 50 to about 95 percent by weight.
More preferably, the H-HDPE is present in an amount of about 55 to about 85 percent by weight.
A suitable HMW-HDPE for use in the melt blends according to the invention has a weight average molecular weight of about 100,000 to about 1,000,000 daltons. As is lmown to those slcilled in the art, the melt flow index of the polymer varies inversely with the molecular weight. According to the invention, the HMW-HDPE is preferably selected based on its melt flow index and density, rather than its particular molecular weight.
Any or all of the LLDPE and/or the LMDPE and the HDPE resins in the embodiments of the invention melt blended compositions can be recycled, wide specification, scrap and/or virgin resin, with mixtures of these source resins being typical. In particular, the use of recycled, wide specification and/or scrap resins is very economical in comparison to the use of virgin resins. Suitable virgin, scrap, recycled and wide specification LLDPE, H-HDPE, and HMW-HDPE are l~nown in the art. Virgin resins are commercially available from, for example, Exxon Mobil Corporation (Irving, TX), Chevron Phillips Chemical Company LP
(Houston, TX), Dow Chemical Company (Midland, MI), Ipiranga Quimica (Porto Alegre, Brazil), Samsung General Chemicals Co., Ltd. (Seosan, Korea), and SABIC Plastic Products (Riyadh, Saudi Arabia).
Exemplary recycled and/or scrap LLDPE and LMDPE can be, but are not limited to, for example, printed plastic dry cleaning bag material, off color plastic bags and the lilce. The visual characteristics of the printed or off color plastic bags are not apparent when used in compositions for applications, including pipe and pipe fittings, where the addition of carbon black or another colorant masl~s the off color material and/or the printing dye. Exemplary recycled and/or scrap HMW-HDPE film used to make plastic bags, such as grocery bags or "T-shirt bags" for the retail clothing industry, and the life, rnay be recycled for use in the melt blends in accordance with the invention. For example, such plastic bags can be constructed of bimodal HMW-HDPE. Other examples of recyclable materials constructed of HMW-HDPE include, but are not limited to, 55 gallon plastic drums. H-HDPE used to male mills jugs or other such containers, for example, may be recycled for use in the melt blends in accordance with the invention.
Wide specification resins differ from on-specification resins in that a wide specification resin is out of the desired specification range for at least one physical property including, but not limited to, density, melt flow index and FRR.
Because on-specification resins are desirable and sometimes necessary for particular applications, they can command a premium price. Therefore, by using wide specification resins in the melt blends of the embodiments of the invention composition, it is possible to achieve a cost savings in comparison to using resins having specified properties. As a non-limiting example, when wide specification LLDPE and/or LMDPE resin is employed, the physical properties of the melt blend compositions are obtained by compensating for the out-of range specification characteristic with a formulation change that can include one or more HDPEs having a corresponding off setting characteristic. For example, to compensate for LLDPE having a melt flow index in a range of 0.4 to 1.0, HDPE
having a low melt flow index of, for example, 0.01 to 0.1 can be employed, or the proportion of HDPE with a melt flow index range of, for example, 0.05 to 0.1 can be increased in the composition. As another example, to compensate for LLDPE
having a density of, for example, 0.920 g/cm3, a 50:50 mixture of the LLDPE
and an H-HDPE having a density of 0.965 g/cm3 can be employed, to bring the density of the final product to 0.945 g/cm3. However, because LLDPE has good stress crack resistance, it is desirable to use a only small amount of, for example, H-HDPE which has a low stress cracl~ resistance. In general, as the density of the HDPE increases, the less is the amount of the HDPE required in the composition to achieve the desired density, melt flow index and other physical properties.
A feature of the invention compositions is that more than one LLDPE, LMDPE, H-HDPE, and/or HMW-HDPE, each b.aving individual ranges of density, MFI and/or FRR and/or modalities, can be employed to increase the flexibility by which components can be melt-blended together in order to achieve the desired physical characteristics of the resulting composition. For example, it is possible to use combinations of resins that include, for example but not limited to, one to about 6 or more individual LLDPEs, LMDPEs, H-HDPEs, and/or HMW-HDPEs.
Once in possession of the teachings herein, including the examples below, of cornponents which can be utilized to achieve the desired physical properties of the melt blend compositions, the selection of suitable components, not limited to those expressly disclosed, will be within the ordinary shill in the art. The invention practitioner will be able to adjust the components of the composition for specification variations without undue experimentation.
The melt-blended compositions of the invention can be used to produce an extruded, molded or formed plastic article having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress cracl~
resistance of at least 24 hours. Exemplary articles include, but are not limited to, pipe, including conduit pipe, pipe fittings, wire insulation material, cable insulation materials, films, sheets, and environmental chambers, especially for applications described above.
The melt-blended compositions of the invention are particularly useful to produce profile or corrugated pipe and/or pipe fittings, having physical properties that conform to applicable standards. As a non-limiting example of pipe and pipe fitting applications, the compositions can be used to produce profile and corrugated pipe having a density of 0.945 to 0.955, a MFI of about 0.1 to 0.4, a minimum flexural modulus of 110,000 psi, a minimum tensile strength of 3,000 psi and a minimum stress crack resistance of at least 24 hours, as required by current AASHTO standards.
Generally, a small diameter extruded pipe (e.g., about 2 inches to about 12 inches) is easier to extrude and form. Thus, a small diameter pipe, for example, can be formed from a melt blend composition of the invention having a MFI of about 0.3 to less than 0.4; whereas a large diameter extruded pipe (e.g., about 36 inches to about 72 inches) should be stiffer for extrusion and forming.
Therefore a large diameter pipe can be formed from a melt blend composition having a MFI of about 0.15 to about 0.2, for example. Medium diameter pipes (e.g., about 15 inches to about 30 inches) can be formed from a melt blend composition having a moderate MFI of about 0.2 to about 0.3, for example.
Similarly, it is generally understood that the processability of corrugated pipe is improved by an increased stiffness of the melt blend, in comparison to the stiffness of the melt blend used to produce profile pipe. Accordingly, one of ordinary slcill in the art could produce pipe according to the invention by varying the proportions of the melt blend components in the melt blend until the desired melt flow index and density of the composition was achieved, without undue experimentation.
Natural ethylene polymers have a detrimental property in that they slowly degrade in the presence of oxygen (air), and the degradation is l~nown to be accelerated by the presence of heat and/or ultraviolet radiation. Preferably, pipes or pipe fittings comprising the melt blended composition are compounded with small amounts of carbon blacl~, or other photo- and thermal-oxidation retarders to minimize the effects of heat and ultra violet light. For example, the composition can comprise carbon black (about 1 percent to about 5 percent, preferably about 2 percent to about 3 percent by weight). The carbon blacks can include any of the commonly available, commercially-produced carbon blacks including, but not limited to, furnace blacks, acetylene blacks, channel blacks and lamp blacks.
The compositions according to the invention may also comprise other additives customary for use in resin-based compositions, according to the application for which they are being used. Such additives include, but are not limited to, antioxidants, antiozonants, lubricants, stabilizers, processing aids, water-proofing fillers, inorganic fillers, colorants, curatives, and the like.
These additives are used in amounts designed to provide their intended effect in the resulting composition. The total amount of such additives can range from zero to about 10 percent by weight based on the total weight of the composition.
In one embodiment, a method for producing a polyethylene composition according to the invention comprises melt blending together a sufficient amount of a HDPE resin and a sufficient amount of at least one additional resin selected from the group consisting of LLDPE resins, LMDPE resins, and mixtures thereof, to produce a melt-blended composition having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours. The HDPE resin can be present in an amount of about 50 to about 95 percent by weight.
In another embodiment, a method for producing a polyethylene composition according to the invention comprises melt blending together a sufficient amount of a HDPE resin selected from the group consisting of a HMW-HDPE resin having a density of about 0.941 to about 0.958 g/cm3 and a melt flow index of about 0.01 to about 0.2, a H-HDPE resin having a density of about 0.957 to about 0.970 g/cm3 and a melt flow index of about 0.1 to about 1.5, and mixtures thereof; and a sufficient amount of at least one additional polyethylene resin having a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3, to produce a melt-blended composition having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress craclc resistance of at least 24 hours. The HDPE resin can be present in an amount of about 50 to about 95 percent by weight.
The LLDPE, LMDPE and HDPE resins can be in pellet, powdered, flake or regrind form, or the like. The methods are not intended to be limited to any one method of melt blending the components. For example, mixing or melt blending of components, including any additives if used, can be by batch 5 compounding, such as in a Banbury or Henschel type mixer, or can be continuous compounding in an extruder. For example, in one embodiment of the method, the components of the composition can be dry-blended prior to melt blending by single screw or twin screw extrusion. In another embodiment, the dry components can be separately fed through separate ports into an extruder for melt 10 blending. In yet another embodiment, the two or more components can be pre-combined in a mixer, such as a Banbury or Henschel mixer, preferably under high intensity blending, to form a hot melt which then can be combined with a third component (e.g., a let down resin) in an extruder. For example, a sufficient amount of LLDPE and H-HDPE can be preblended in a Banbury mixer, and the 15 resulting composition blended with a sufficient amount of HMW-HDPE in an extruder to produce the desired percentages of each of the three types of components in the final composition. Moreover, any of the components can be mixed with, for example, carbon black or other colorants and/or other additives, as a master batch, which is then added to a let down resin comprising one or more of the remaining components, to produce the desired percentages of the components in the final composition. As a non-limiting example, 25% of a master batch composition comprising 90% LLDPE and 10% carbon blaclc can be combined with 75% HDPE let down resin to provide the desired amount of LLDPE, HDPE and carbon black in the final composition to provide the desired properties of density and melt flow index. The temperatures and other variables required for dry blending, hot melts, and melt blending are well known to those skilled in the art.
Following melt blending of the components, the composition can be inj ection molded, blow molded, rolled, milled, sheet extruded, film extruded, pipe extruded, or formed or fabricated in any manner whatsoever to form the desired product by known methods. Once the teachings herein are in hand, the skilled practitioner of this invention will be able to adapt conventional methods of forming material, such as inj ection molding and other techniques mentioned above, to the production of desired articles of manufacture using the polyethylene composition of the invention. This adaptation can be implemented on an empirical basis, without undue experimentation.
S EXAMPLES
The following examples illustrate methods of preparation of melt blended polyethylene compositions of the invention. However, the examples are not intended to be limiting, as other methods for preparing these compounds and different compounding formulations may be determined by those spilled in the art. Further, the blend components are not limited to the specific polyethylenes shown. Thus, it is believed that any of the variables disclosed herein can readily be determined and controlled without departing from the scope of the invention herein disclosed and described.
Below are three examples of preferred embodiments in which the mix 1S ratios of LLDPE, H-HDPE and HMW-HDPE components differ with respect to each other. In each of the following examples, the exemplary polyethylene was _ prepared under industry standard conditions using melt blending techniques as known in the art. Dry mixtures of pelletized LLDPE and HDPEs were introduced directly into a profile extruder to produce HDPE pipe.
The H-HDPE used in all of the following examples was Grade GD 4960, supplied by Ipiranga Quimica (1'orto Alegre, Brazil), having a melt flow index of 0.80 and a density of 0.962 g/cm3. The HMW-HDPE used in all of the examples was grade F120A, supplied by Samsung General Chemicals Co., Ltd. (Seosan, Korea), having a melt flow index of 0.044 and a density of 0.956 g/cm3. The 2S LLDPE used in all of the examples was Grade 726N, supplied by SABIC Plastic Products (a division of Saudi Arabia Basic Industries Corporation, Riyadh, Saudi Arabia), having a melt flow index of 0.70 and a density of 0.926 g/cm3.
Example 1 The percentages by weight of the polyethylene components used to produce a melt-blended polyethylene composition suitable for a producing a pipe having a diameter of about 24 to about 30 inches are listed below. The physical properties of the resulting melt-blended polyethylene composition are illustrated in Table 1.
35% H-HDPE
20% HMW-HDPE
45% LLDPE
Example 2 The percentages by weight of the polyethylene components used to produce a melt-blended polyethylene composition suitable for a producing a pipe having a diameter of about 12 to about 1S inches are listed below. The physical properties of the resulting melt-blended polyethylene composition are illustrated in Table 1.
40% H-HDPE
40% HMW-HDPE
20% LLDPE
Example 3 The percentages by weight of the polyethylene components used to produce a melt-blended polyethylene composition suitable for a producing a pipe having a diameter of about 36 to about 72 inches are listed below. The physical properties of the resulting melt-blended polyethylene composition are illustrated in Table 1.
3 5 % H-HDPE
5 5 % HMW-HDPE
10% LLDPE
Physical properties of the melt-blended polyethylene compositions Test Property Units Method Example Example Example -(ASTM) Density g/cm3 D1505 0.945 0.952 0.955 MFR (190 C) g/10 D1238 0.4 0.25 0.15 min NCTL hours D5397 >24 >24 >24 Tensile Strengthpsi D 638 3000 3200 3500 Flexural Moduluspsi D 790 110,000 135,000 160,000 Notched Izod ft-lb/inD 256 5 4 3 Cell Classificationn/a D3350 335400 335400 335400 Flow Rate Ration/a D1238 80 90 110 This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to male and use the invention. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art.
Such other examples are intended to be within the scope of the claims if they have elements that do not differ from the literal language of the claims, or if they include equivalent elements with insubstantial differences from the literal language of the claims.
Such other examples are intended to be within the scope of the claims if they have elements that do not differ from the literal language of the claims, or if they include equivalent elements with insubstantial differences from the literal language of the claims.
Claims (46)
1. A polyethylene composition comprising a melt blend of a high density polyethylene resin and at least one resin selected from the group consisting of linear low density polyethylene resins, linear medium density polyeth-ylene resins, and mixtures thereof, said resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
2. The composition of claim 1, wherein the resins are independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
3. The composition of claim 1, wherein the at least one resin has a melt flow index of about 0.1 to about 1.5.
4. The composition of claim 1, wherein the at least one resin has a density of about 0.920 to about 0.940.
5. The composition of claim 1, wherein the high density polyethylene resin has a melt flow index of about 0.01 to about 1.5.
6. The composition of claim 1, wherein the high density polyethylene resin is selected from the group consisting of a unimodal resin, a bimodal resin, a multimodal resin, and mixtures thereof.
7. The composition of claim 1, wherein the high density polyethylene resin is present in an amount of about 50 to about 95 percent by weight.
8. The composition of claim 1, wherein the flow rate ratio of the melt-blended composition is about 80 to about 130.
9. The composition of claim 1, wherein the flow rate ratio of the resins is about 20 to about 200.
10. The composition of claim 9, wherein the flow rate ratio of the resins is about 90 to about 130.
11. The composition of claim 1, wherein the flow rate ratio of the linear low density polyethylene and the linear medium density polyethylene is about 20 to about 60.
12. The composition of claim 1, wherein the melt flow index of the melt-blended composition is about 0.15 to about 0.35.
13. The composition of claim 12, wherein the melt flow index of the melt-blended composition is about 0.2 to about 0.3.
14. The composition of claim 1, wherein the density of the melt-blended com-position is 0.945 to 0.955 and the melt flow index is about 0.1 to 0.4.
15. The composition of claim 1, wherein the high density polyethylene resin is selected from the group consisting of a high molecular weight high density polyethylene resin having a melt flow index of about 0.01 to about 0.2, a homopolymer high density polyethylene resin having a melt flow index of about 0.1 to about 1.5, and mixtures thereof.
16. The composition of claim 15, wherein the high molecular weight high density polyethylene resin has a density of about 0.941 to about 0.958 g/cm3.
17. The composition of claim 15, wherein the homopolymer high density polyethylene resin has a density of about 0.957 to about 0.970 g/cm3.
18. The composition of claim 15, wherein the high density polyethylene resins are independently selected from the group consisting of a unimodal resin, a bimodal resin, a multimodal resin, and mixtures thereof.
19. The composition of claim 15, wherein the high density polyethylene resins are independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
20. A polyethylene composition comprising a melt blend of (a) a high density polyethylene resin selected from the group consist-ing of a high molecular weight high density polyethylene resin having a density of about 0.941 to about 0.958 g/cm3 and a melt flow index of about 0.01 to about 0.2, a homopolymer high density polyethylene resin having a density of about 0.957 to about 0.970 g/cm3 and a melt flow index of about 0.1 to about 1.5, and mixtures thereof; and (b) at least one additional polyethylene resin having a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3, said polyethylene resins being present in the melt-blended composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
21. The composition of claim 20, wherein the high density polyethylene resin is present in an amount of about 50 to about 95 percent by weight.
22. The composition of claim 20, wherein the resins are independently se-lected from the group consisting of virgin, recycled, scrap and wide speci-fication resins, and mixtures thereof.
23. An extruded, molded or formed plastic article comprising a melt blended polyethylene composition that comprises a melt blend of a high density polyethylene resin and at least one resin selected from the group consisting of linear low density polyethylene resins, linear medium density polyeth-ylene resins, and mixtures thereof, said resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
24. The article of claim 23, wherein the article is selected from the group con-sisting of pipe, pipe fittings, wire insulation material, cable insulation ma-terials, films, sheets, and environmental chambers.
25. The article of claim 23, wherein the resins are independently selected from the group consisting of virgin, scrap, recycled, and wide specification res-ins, and mixtures thereof.
26. An extruded, molded or formed plastic article comprising a melt blended polyethylene composition that comprises a high density polyethylene resin selected from the group consisting of a high molecular weight high density polyethylene resin having a density of about 0.941 to about 0.958 g/cm3 and a melt flow index of about 0.01 to about 0.2, a homopolymer high density polyethylene resin having a density of about 0.957 to about 0.970 g/cm3 and a melt flow index of about 0.1 to about 1.5, and mixtures thereof; and at least one additional polyethylene resin having a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3, said polyethylene resins being present in the melt-blended compo-sition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
27. The article of claim 26, wherein the article is selected from the group con-sisting of pipe, pipe fittings, wire insulation material, cable insulation ma-terials, films, sheets, and environmental chambers.
28. The article of claim 26, wherein the resins are independently selected from the group consisting of virgin, scrap, recycled, and wide specification res-ins, and mixtures thereof.
29. An extruded, molded or formed pipe and/or pipe fitting comprising a melt blended polyethylene composition that comprises a melt blend of a high density polyethylene resin and at least one resin selected from the group consisting of linear low density polyethylene resins, linear medium density polyethylene resins, and mixtures thereof, said resins being present in the melt-blended polyethylene composition in amounts relative to one another such that the composition has a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack re-sistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
30. The pipe and/or pipe fitting of claim 29, wherein the resins are independ-ently selected from the group consisting of virgin, scrap, recycled, and wide specification resins, and mixtures thereof.
31. The pipe and/or pipe fitting of claim 29, wherein the composition further comprises about 1 to about 5 percent by weight carbon black.
32. The pipe and/or pipe fitting of claim 29, wherein the pipe is selected from the group consisting of profile pipe, corrugated pipe, and combinations thereof.
33. The pipe and/or pipe fitting of claim 29, having a density of 0.945 to 0.955, a melt flow index of about 0.1 to 0.4, a minimum flexural modulus of 110,000 psi and a minimum tensile strength of 3,000 psi.
34. The pipe and/or pipe fitting of claim 33, wherein the pipe is selected from the group consisting of profile pipe, corrugated pipe, and combinations thereof.
35. An extruded, molded or formed pipe and/or pipe fitting comprising a melt blended polyethylene composition that comprises a high density polyeth-ylene resin selected from the group consisting of a high molecular weight high density polyethylene resin having a density of about 0.941 to about 0.958 g/cm3 and a melt flow index of about 0.01 to about 0.2, a homo-polymer high density polyethylene resin having a density of about 0.957 to about 0.970 g/cm3 and a melt flow index of about 0.1 to about 1.5, and mixtures thereof; and at least one additional polyethylene resin having a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3, said polyethylene resins being present in the melt-blended composition in amounts relative to one another such that the com-position has a density of about 0.945 to about 0.960 g/cm3, a melt flow in-dex of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
36. The pipe and/or pipe fitting of claim 35, wherein the resins are independ-ently selected from the group consisting of virgin, scrap, recycled, and wide specification resins, and mixtures thereof.
37. The pipe and/or pipe fitting of claim 35, wherein the composition further comprises about 1 to about 5 percent by weight carbon black.
38. The pipe and/or pipe fitting of claim 35, wherein the pipe is selected from the group consisting of profile pipe, corrugated pipe, and combinations thereof.
39. The pipe and/or pipe fitting of claim 35, having a density of 0.945 to 0.955, a melt flow index of about 0.1 to 0.4, a minimum flexural modulus of 110,000 psi and a minimum tensile strength of 3,000 psi.
40. The pipe and/or pipe fitting of claim 39, wherein the pipe is selected from the group consisting of profile pipe, corrugated pipe, and combinations thereof.
41. A method for producing a polyethylene composition, comprising melt blending together a sufficient amount of a high density polyethylene resin and a sufficient amount of at least one additional resin selected from the group consisting of linear low density polyethylene resins, linear medium density polyethylene resins, and mixtures thereof, to produce a melt-blended composition having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
42. The method of claim 41, wherein the resins are independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
43. The method of claim 41, wherein the high density polyethylene resin is present in an amount of about 50 to about 95 percent by weight.
44. A method for producing a polyethylene composition, comprising melt blending together a sufficient amount of a high density polyethylene resin selected from the group consisting of a high molecular weight high density polyethylene resin having a density of about 0.941 to about 0.958 g/cm3 and a melt flow index of about 0.01 to about 0.2, a homopolymer high density polyethylene resin having a density of about 0.957 to about 0.970 g/cm3 and a melt flow index of about 0.1 to about 1.5, and mixtures thereof; and a sufficient amount of at least one additional polyethylene resin having a melt flow index of about 0.1 to about 1.5 and a density of about 0.920 to about 0.940 g/cm3, to produce a melt-blended composition having a density of about 0.945 to about 0.960 g/cm3, a melt flow index of about 0.1 to about 0.4, and a stress crack resistance of at least 24 hours wherein the melt flow index is measured according to ASTM D1238 and the stress crack resistance is measured according to ASTM D1693, ASTM D5397, or ASTM D2561.
45. The method of claim 44, wherein the resins are independently selected from the group consisting of virgin, recycled, scrap and wide specification resins, and mixtures thereof.
46. The method of claim 44, wherein the high density polyethylene resin is present in an amount of about 50 to about 95 percent by weight.
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| US10/022,706 US20030113496A1 (en) | 2001-12-17 | 2001-12-17 | Polyethylene melt blends for high density polyethylene applications |
| US10/022,706 | 2001-12-17 | ||
| PCT/US2002/031652 WO2004016688A2 (en) | 2001-12-17 | 2002-10-03 | Polyethylene melt blends for high density polyethylene applications |
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| CA2470180A1 true CA2470180A1 (en) | 2004-02-26 |
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-
2001
- 2001-12-17 US US10/022,706 patent/US20030113496A1/en not_active Abandoned
-
2002
- 2002-10-03 AU AU2002368161A patent/AU2002368161A1/en not_active Abandoned
- 2002-10-03 CA CA002470180A patent/CA2470180A1/en not_active Abandoned
- 2002-10-03 BR BR0215056-5A patent/BR0215056A/en not_active IP Right Cessation
- 2002-10-03 MX MXPA04006011A patent/MXPA04006011A/en not_active Application Discontinuation
- 2002-10-03 WO PCT/US2002/031652 patent/WO2004016688A2/en not_active Application Discontinuation
- 2002-10-03 CN CN02828138.1A patent/CN1620476A/en active Pending
- 2002-10-03 EP EP02807661A patent/EP1458807A2/en not_active Withdrawn
-
2007
- 2007-05-22 US US11/802,426 patent/US7867588B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US20080114131A1 (en) | 2008-05-15 |
| WO2004016688A3 (en) | 2004-07-01 |
| MXPA04006011A (en) | 2005-02-24 |
| AU2002368161A1 (en) | 2004-03-03 |
| EP1458807A2 (en) | 2004-09-22 |
| CN1620476A (en) | 2005-05-25 |
| BR0215056A (en) | 2004-12-14 |
| US7867588B2 (en) | 2011-01-11 |
| WO2004016688A2 (en) | 2004-02-26 |
| US20030113496A1 (en) | 2003-06-19 |
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| EEER | Examination request | ||
| FZDE | Discontinued |