|Publication number||USH1518 H|
|Application number||US 08/304,974|
|Publication date||Feb 6, 1996|
|Filing date||Sep 13, 1994|
|Priority date||Nov 3, 1993|
|Publication number||08304974, 304974, US H1518 H, US H1518H, US-H-H1518, USH1518 H, USH1518H|
|Inventors||Lie K. Djiauw, Michael J. Modic, Richard Gelles, Glenn R. Himes|
|Original Assignee||Shell Oil Company|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (11), Referenced by (1), Classifications (7), Legal Events (5)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This is a continuation of application Ser. No. 08/150,654, filed Nov. 3, 1993, now abandoned.
The invention relates to compositions that contain polyolefin resins and elastomeric block copolymers. More specifically, the invention relates to polypropylene molding compositions that have improved impact resistance.
Polypropylene molding compositions containing low or medium flow polypropylene have good impact resistance when the composition includes a high molecular weight styrenic block copolymer having the structure polystyrene-hydrogenated polybutadiene-polystyrene, e.g. KRATON® G1650 thermoplastic elastomer. The impact strengths are suitable for use of the molding compositions in large automotive parts. However, research has established that polypropylene molding compositions for large automotive parts must also have improvements in rigidity, heat deformation resistance, low temperature impact resistance, and surface appearance.
High flow polypropylene molding compositions that are suitable for large automotive parts except for inferior low temperature impact strength and inferior high temperature heat deformation are produced by blending low molecular weight polystyrene with low molecular weight diblock copolymers of polystyrene-hydrogenated butadiene. A blend of the triblock and diblock copolymers is commercially available as KRATON® G1657 elastomer which is available from Shell.
U.S. Pat. No. 5,045,589 describes much improved polypropylene molding compositions comprising a crystalline ethylene/propylene block copolymer, an amorphous polypropylene copolymer, and a thermoplastic elastomer which can be a polystyrene-hydrogenated polybutadiene-polystyrene elastomer, e.g. KRATON® G1650 elastomer, or a polystyrene-hydrogenated polyisoprene-polystyrene elastomer.
The present invention provides a high flow polypropylene molding composition that is excellent for large automobile parts, the polypropylene composition containing a low molecular weight polystyrene-hydrogenated polyisoprene-polystyrene elastomer which is superior to butadiene based elastomers for improving low temperature impact strength and high temperature heat distortion. The isoprene based triblock polymers are also excellent modifiers for blends containing ethylene/propylene block polymers.
Polypropylene molding compositions comprising 60-95%, preferably 80-95%, by weight of the polymer components of a high flow polypropylene homopolymer or copolymer and 40-5%, preferably 20-5%, by weight of the polymer components of a low molecular weight polystyrene-hydrogenated polyisoprene-polystyrene block copolymer have excellent physical and appearance properties including superior low temperature impact strength and superior high temperature heat deformation. The peak molecular weight of the block copolymers ranges from 58,000 to 82,000 with a polystyrene content from 13% to 20%.
The high flow propylene polymer can be (i) a homopolymer of propylene, (ii) a random copolymer of propylene and an olefin selected from ethylene and C4 -C10 alpha-olefins, or (iii) a random terpolymer of propylene with two alpha-olefins selected from the group consisting of ethylene and C4 -C10 alpha olefin, provided that the propylene polymer has a melt flow higher than 30 dg/min as measured by ASTM Method D 1238-82 (230° C./5 kg). Preferably, the polypropylene has a melt flow from 50 to 80 dg/min. The C4 -C10 alpha-olefins include linear and branched C4 -C10 alpha-olefins such as 1-butene, 1-pentene, 4-methyl-pentene-1, 3-methyl-1-butene, 1-hexene, 3-4-dimethyl-1-butene, 1-heptene, 3-methyl-1-hexene, 1-octene and the like.
The elastomeric block copolymers employed in the molding compositions of the present invention have two polystyrene endblocks and one hydrogenated isoprene midblock in a linear arrangement (S-EP-S). The polystyrene endblocks each preferably have a peak molecular weight from 4,500 to 8,000, most preferably from 5,000 to 5,500, which results in formation of weak polystyrene domains and low melt viscosity.
The hydrogenated isoprene blocks have a residual unsaturation less that 5%, preferably less than 2%, and may have from 30% to 100% 1,4-addition of the isoprene. The block copolymers are readily prepared by anionic polymerization and selective hydrogenation processes known in the art to give polymers having low polydispersity.
The polypropylene molding compositions could further contain polyethylene-polypropylene block copolymers as described in U.S. Pat. No. 5,045,589 which is incorporated by reference herein.
Fillers and reinforcing agents, e.g. carbon black and glass fibers, as well as inorganic powders such as calcium carbonate, talc, mica, and glass, may be included in the composition of the invention at concentration levels up to about 80 parts by weight per 100 parts by weight of the total polymer components. In addition to the economic benefit such fillers afford, greater stiffness and a higher heat distortion temperature can be attained.
The components of the composition can be blended or admixed in any conventional mixing apparatus, such as an extruder or a Banbury mixer.
The following examples, presented for illustrative purposes, describe various embodiments of the polypropylene molding composition of the invention.
In all of the examples and control experiments, the polypropylene and the S-EP-S block copolymer, as well as any other modifier used in comparison, were mixed and extruded in a single pass through a co-rotating twin-screw extruder. A stabilizer composition (0.08 weight%), known as Irganox 1010, was added to all batches before compounding to minimize oxidation. The extruder temperature was in the 200°-245° C. range. The extruded blends were molded into test specimens.
The test methods used to evaluate the molded specimens were ASTM D-256 (notched Izod impact at room temperature), ASTM D-638 (tensile strength), ASTM D-790 (flexural modulus), and ASTM-648 (Heat Distortion Temperature at 1820 kPa).
Two polypropylene molding compositions of the invention were made and tested as described above. In these compositions the block copolymer was a S-EP-S block copolymer. Two control compositions containing known styrene/butadiene block copolymers also were made and tested in the same manner.
The propylene polymer used in the preparation of the molding compositions was a pelletized polypropylene resin, commercially available from UBE (UBE ZT772), a nominal melt flow rate (ASTM Method D 1238-82, 230° C./5 kg) of 66 dg/min.
The block copolymers are further described in Table I and the polypropylene molding compositions and results of the evaluations performed on the Example 1-2 compositions and the two control compositions are shown in Table II.
TABLE I__________________________________________________________________________ Comparison Example No. Example No. A.sup.(a) B.sup.(b) 1 2__________________________________________________________________________Triblock/Diblock in 100% S-EB-S 70% S-EB-S 100% S-EP-S 100% S-EP-SBlock Copolymer (wt %) 30% S-EBMolecular Weight (peak) 71,000 82,000 62,000 59,000Triblock/Diblock 41,000Polystyrene (wt %).sup.(c) 30 13 18 19Melt Flow dg/min.sup.(d) No Flow 20-29 14 29Tensile strength psi 3,100 2,550 3,100 3,125__________________________________________________________________________ .sup.(a) Commercially availableKRATON ® G1650 elastomer from Shell. .sup.(b) Commercially availableKRATON ® G1657 elastomer from Shell. .sup.(c) Measured prior to hydrogenation. .sup.(d) ASTM D1238 (230° C./5 kg).
TABLE II______________________________________ Comparison Example No. Example No.Polypropylene Comp..sup.(a) A B 1 2______________________________________Heat Distortion Temperature 109.0 104.1 105.6 --(°C.)Brittleness Temp. (°C.) -37.6 -40.8 -45.0 --Izod Impact (Kg-cm/cm.sup.2) 15.8 21 38 57Melt Flow dg/min.sup.(b) 40 59 57 60Flex Modulus (Kg/cm.sup.2) 12,450 12,070 12,040 11,410______________________________________ .sup.(a) Contains 90% high flow polypropylene and 10% block copolymer wit 0.08% Irganox 1010. .sup.(b) ASTM 1238 230° C./5 kg.
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|Citing Patent||Filing date||Publication date||Applicant||Title|
|US20150315377 *||Mar 30, 2015||Nov 5, 2015||Exxonmobil Chemical Patents Inc.||Polypropylene Compositions and Methods to Produce the Same|
|International Classification||C08L53/00, C08L53/02, C08L23/10|
|Cooperative Classification||C08L53/02, C08L23/10|
|Jul 17, 1995||AS||Assignment|
Owner name: SHELL OIL COMPANY, TEXAS
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:DJIAUW, LIE KHONG;MODIC, MICHAEL JOHN;GELLES, RICHARD;AND OTHERS;REEL/FRAME:007579/0927
Effective date: 19940103
|Jan 2, 2004||AS||Assignment|
Owner name: UBS AG, STAMFORD BRANCH, CONNECTICUT
Free format text: SECURITY INTEREST;ASSIGNOR:KRATON POLYMERS U.S. LLC;REEL/FRAME:014242/0281
Effective date: 20031223
|Mar 26, 2009||AS||Assignment|
Owner name: KRATON POLYMERS U.S. LLC, TEXAS
Free format text: AFFIDAVIT OF NAME CHANGE;ASSIGNOR:SHELL ELASTOMERS LLC;REEL/FRAME:022452/0984
Effective date: 20090323
Owner name: SHELL ELASTOMERS LLC, TEXAS
Free format text: CHANGE OF NAME;ASSIGNOR:SHELL OIL COMPANY;REEL/FRAME:022452/0851
Effective date: 20010228
|Feb 24, 2011||AS||Assignment|
Owner name: KRATON POLYMERS U.S. LLC, TEXAS
Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:UBS AG, STAMFORD BRANCH;REEL/FRAME:025845/0795
Effective date: 20110211
|Dec 16, 2015||AS||Assignment|
Owner name: KRATON POLYMERS U.S. LLC, TEXAS
Free format text: CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NUMBER 7720798 AND REPLACE WITH PATENT NUMBER7220798 PREVIOUSLY RECORDED ON REEL 025845 FRAME 0795. ASSIGNOR(S) HEREBY CONFIRMS THE RELEASE BY SECURED PARTY;ASSIGNOR:USB AG, STAMFORD BRANCH;REEL/FRAME:037312/0070
Effective date: 20110211