WO2007140127A1 - Thermoplastic elastomers for adhesion to polyamide - Google Patents
Thermoplastic elastomers for adhesion to polyamide Download PDFInfo
- Publication number
- WO2007140127A1 WO2007140127A1 PCT/US2007/069097 US2007069097W WO2007140127A1 WO 2007140127 A1 WO2007140127 A1 WO 2007140127A1 US 2007069097 W US2007069097 W US 2007069097W WO 2007140127 A1 WO2007140127 A1 WO 2007140127A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- styrene
- compound
- polyamide
- ethylene
- molecular weight
- Prior art date
Links
- 229920002725 thermoplastic elastomer Polymers 0.000 title claims abstract description 34
- 239000004952 Polyamide Substances 0.000 title claims description 17
- 229920002647 polyamide Polymers 0.000 title claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 32
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 9
- 239000004014 plasticizer Substances 0.000 claims description 8
- -1 styrene-ethylene-butylene-styrene Chemical class 0.000 claims description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 5
- 239000000945 filler Substances 0.000 claims description 4
- 239000003063 flame retardant Substances 0.000 claims description 4
- 239000013032 Hydrocarbon resin Substances 0.000 claims description 3
- 229920006270 hydrocarbon resin Polymers 0.000 claims description 3
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 claims description 2
- UHKPXKGJFOKCGG-UHFFFAOYSA-N 2-methylprop-1-ene;styrene Chemical compound CC(C)=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 UHKPXKGJFOKCGG-UHFFFAOYSA-N 0.000 claims description 2
- 239000004604 Blowing Agent Substances 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 239000004606 Fillers/Extenders Substances 0.000 claims description 2
- 239000004609 Impact Modifier Substances 0.000 claims description 2
- 239000002318 adhesion promoter Substances 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 239000003139 biocide Substances 0.000 claims description 2
- 239000002981 blocking agent Substances 0.000 claims description 2
- 238000007664 blowing Methods 0.000 claims description 2
- 239000007767 bonding agent Substances 0.000 claims description 2
- FACXGONDLDSNOE-UHFFFAOYSA-N buta-1,3-diene;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 FACXGONDLDSNOE-UHFFFAOYSA-N 0.000 claims description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- 239000003999 initiator Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- 239000003921 oil Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 150000004756 silanes Chemical class 0.000 claims description 2
- 239000000779 smoke Substances 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 claims description 2
- 229940124543 ultraviolet light absorber Drugs 0.000 claims description 2
- 239000001993 wax Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 abstract description 18
- 238000007906 compression Methods 0.000 abstract description 7
- 230000006835 compression Effects 0.000 abstract description 7
- 229920002292 Nylon 6 Polymers 0.000 abstract description 4
- 229920002302 Nylon 6,6 Polymers 0.000 abstract description 3
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 17
- 229920002633 Kraton (polymer) Polymers 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 229920001169 thermoplastic Polymers 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 2
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 235000019589 hardness Nutrition 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 229920002397 thermoplastic olefin Polymers 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- 229920006342 thermoplastic vulcanizate Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920002743 polystyrene-poly(ethylene-ethylene/propylene) block-polystyrene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
Definitions
- This invention relates to thermoplastic elastomers, polymer compounds which exhibit elasticity while remaining thermoplastic.
- thermoplastic elastomers combine the benefits of elastomeric properties of thermoset polymers, such as vulcanized rubber, with the processing properties of thermoplastic polymers.
- two-part component extrusion or molding has recently become popular to provide one type of rheology in one part of the component and a second type of rheology in a second part of the component.
- a specific use of two-part component thermoplastic compounds is insulating strips for vehicle doors.
- One part has a relatively rigid rheological structure for securing the component to the door, with the second part being a relative flexible rheological structure to compress and seal the door to the vehicle.
- Polyamide also called nylon, is an excellent polymer for the relatively rigid rheological structure. But nylon is notorious for being difficult to adhere to other types of polymers, particularly thermoplastic elastomers that are useful for the relatively flexible rheological structure of an insulation strip for an automobile door seal.
- thermoplastic elastomer also called "TPE”
- TPE thermoplastic elastomer
- the present invention solves the problem by formulating a TPE that provides excellent adhesion to polyamide (also called "PA").
- thermoplastic elastomer compound comprising (a) high molecular weight maleated styrene-ethylene- butylene-styrene; (b) plasticizer; (c) processing aid; and (d) polyamide, also optionally but preferably further comprising styrene-containing thermoplastic elastomer.
- Another aspect of the invention is a two-component article, comprising the above compound as one component and polyamide as the second component
- TPE styrene
- MAH-g-SEBS low molecular weight maleated styrene- ethylene-butylene- styrene
- a commercial example of low molecular weight maleated SEBS is Kraton FG 190 Ix, having a weight average molecular weight of about 76,900.
- high molecular weight maleated SEBS Kraton MD6684CS
- Kraton MD6684CS has a weight average molecular weight of about 250,000. Therefore, for purposes of this invention, "high molecular weight" for maleated SEBS means a weight average molecular weight of at least about 200,000. Desirably, the "high molecular weight” is at least about 225,000, and preferably at least about 250,000.
- TPE-S are a complex combination of TPE, compatibilizer, plasticizer, processing aid, filler, antioxidant, antiblocking agent, and one or more secondary polymers.
- the present invention replaces the LMW MAH-g-SEBS with a
- HMW MAH-g-SEBS serving as a compatibilizer and introduces a secondary polymer, preferably PA which assists in compatibilization.
- TPE-S include styrene-ethylene- butylene-styrene, styrene-ethylene-propylene-styrene, styrene-ethylene- ethylene/propylene-styrene, styrene-isobutylene-styrene, styrene-butadiene- styrene, styrene-isoprene-styrene, and combinations thereof.
- TPE-S are not maleated but have weight average molecular weights in excess of 100.000 and preferably in excess of 200,000.
- Commercially available grades of these TPE-S compounds are Kraton Gl 651 and Kraton MD 6933 from Kraton Polymers and Septon 4077 and Septon 4099 from Kuraray.
- An example of HMW MAH-g-SEBS is Kraton MD6684CS.
- SEBS is also applicable to other types of TPEs, among them thermoplastic vulcanizates (TPVs), thermoplastic polyurethanes (TPUs), and thermoplastic olefins (TPOs), except that the TPE portion of the high molecular weight compatibilizer will need to be adjusted, as needed, to be compatible with the type of TPE employed.
- TEVs thermoplastic vulcanizates
- TPUs thermoplastic polyurethanes
- TPOs thermoplastic olefins
- Any conventional plasticizer preferably a paraffinic oil, is suitable for use the present invention.
- a preferred processing aid is a hydrocarbon resin, preferably a rosin ester, because it improves process ability of the compound within the mixing vessel, a particular problem with high molecular weight TPEs.
- a preferred secondary polymer for the present invention is polyamide, as mentioned above, because the polyamide promotes adhesion to polyamide-containing other component of the two-part component molded or extruded article.
- the compound of the present invention can include conventional plastics additives in an amount that is sufficient to obtain a desired processing or performance property for the compound.
- the amount should not be wasteful of the additive nor detrimental to the processing or performance of the compound.
- Non-limiting examples of optional additives include adhesion promoters; biocides (antibacterials, fungicides, and mildewcides), anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppresants; impact modifiers; initiators; lubricants; micas; pigments, colorants and dyes; plasticizers; processing aids; release agents; silanes, titanates and zirconates; slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; and combinations of them.
- adhesion promoters include adhesion promoters; biocides (antibacterials, fungicides, and mildewcides), anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppresants; impact modifiers;
- Table 1 shows the acceptable, desirable, and preferable ranges of ingredients for the TPE of the present invention.
- the preparation of compounds of the present invention is uncomplicated.
- the compound of the present can be made in batch or continuous operations.
- Mixing in a continuous process typically occurs in an extruder that is elevated to a temperature that is sufficient to melt the polymer matrix with addition of all additives at the feed-throat, or by injection or side-feeders downstream.
- Extruder speeds can range from about 50 to about 500 revolutions per minute (rpm), and preferably from about 100 to about 300 ipm.
- the output from the extruder is pelletized for later extrusion or molding into polymeric articles.
- Mixing in a batch process typically occurs in a Banbury mixer that is also elevated to a temperature that is sufficient to melt the polymer matrix to permit homogenizat ⁇ on of the compound components.
- the mixing speeds range from 60 to 1000 rpm and temperature of mixing can be ambient. Also, the output from the mixer is chopped into smaller sizes for later extrusion or molding into polymeric articles.
- TPE-S of the present invention is an excellent one part of a two- part component polymer structure because it has excellent adhesion to polyamides including polyamide 6, polyamide 66, polyamide 11, polyamide 12 and others, which is often used as the more rigid part of the structure.
- two-part component polymer structures are used in the following industrial and consumer products: power tool grips, integrated seals and gaskets, anti- vibration mounts, automotive interior trim, sound deadening parts, glazing gaskets, flexible membranes, and other articles now or hereafter known.
- Table 2 shows five examples of the present invention, in comparison with a control (Comparative Example A) representing a traditional TPE-S that is commercially available.
- LMW MAH-g-SEBS is attributed to a desire to the improved performance at elevated temperatures of HMW MAH-g-SEBS.
- polyamide was injected first into a custom designed tool with a moving core, after which the TPE compound was injected directly onto the polyamide.
- the two-component (“2K") test bars were ejected and conditioned at room temperature for 24 hours. After conditioning, an attempt was made by hand to remove the TPE strip from the polyamide substrate, and the difficulty noted. Additionally it was noted whether the bond failed by adhesive failure (where the TPE is cleanly removed from the substrate) or by cohesive failure (where a layer of TPE remains on the substrate, the interfacial strength is higher than the cohesive strength of the TPE, the optimal case).
- Examples 1-5 exhibit a variety of hardnesses as well as excellent adhesion to both polyamide 6 and polyamide 6,6, two of the most popular grades of polyamide. Comparative Example A only adheres well to polyamide 6.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyamides (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
A thermoplastic elastomer (TPE) is disclosed which has excellent compression set and adhesion to both polyamide 6 and polyamide 6,6 for use in two-part component polymer structures.
Description
THERMOPLASTIC ELASTOMERS FOR ADHESION TO POLYAMIDE
CLAIM OF PRIORITY
[0001] This application claims priority from U.S. Provisional Patent
Application Serial Number 60/803,449 bearing Attorney Docket Number 12006008 and filed on May 30, 2006, which is incorporated by reference.
FIELD OF THE INVENTION
[0002] This invention relates to thermoplastic elastomers, polymer compounds which exhibit elasticity while remaining thermoplastic.
BACKGROUND OF THE INVENTION
[0003] TIi e world of polymers has progressed rapidly to transform material science from wood and metals of the 19th Century to the use of thermoset polymers of the mid-20th Century to the use of thermoplastic polymers of later 20lh Century.
[0004] Thermoplastic elastomers combine the benefits of elastomeric properties of thermoset polymers, such as vulcanized rubber, with the processing properties of thermoplastic polymers.
[0005] Different types of polymers can serve different purposes when combined into a single construction. For example, "two-part component" extrusion or molding has recently become popular to provide one type of rheology in one part of the component and a second type of rheology in a second part of the component. A specific use of two-part component thermoplastic compounds is insulating strips for vehicle doors. One part has a relatively rigid rheological structure for securing the component to the door, with the second part being a relative flexible rheological structure to compress and seal the door to the vehicle.
[OΘ06J Polyamide, also called nylon, is an excellent polymer for the relatively rigid rheological structure. But nylon is notorious for being difficult to adhere to other types of polymers, particularly thermoplastic elastomers that are useful for the relatively flexible rheological structure of an insulation strip for an automobile door seal.
SUMMARY OF THE INVENTION
[0007] What the art needs is a new formulation of thermoplastic elastomer (also called "TPE") that can adhere to polyamide-containing compounds, in order to form excellent two-part component extruded or molded parts.
[0008] The present invention solves the problem by formulating a TPE that provides excellent adhesion to polyamide (also called "PA").
[0009] One aspect of the invention is a thermoplastic elastomer compound, comprising (a) high molecular weight maleated styrene-ethylene- butylene-styrene; (b) plasticizer; (c) processing aid; and (d) polyamide, also optionally but preferably further comprising styrene-containing thermoplastic elastomer.
[00010] Another aspect of the invention is a two-component article, comprising the above compound as one component and polyamide as the second component
[00011] Features of the invention will become apparent with reference to the following embodiments.
EMBODIMENTS OF THE INVENTION
[00012] TPE and Compatibilizer
[00013] One type of TPE is based on styrene (also called "TPE-S"). In traditional TPE formulations, use of a low molecular weight maleated styrene- ethylene-butylene- styrene ("MAH-g-SEBS") as a corapatibilizer resulted in a poor compression set at elevated temperatures (typically >80% at 700C, and
>90% at 1000C). A commercial example of low molecular weight maleated SEBS ("LMW MAH-g-SEBS") is Kraton FG 190 Ix, having a weight average molecular weight of about 76,900.
[00014] However, the recent commercialization of a high molecular weight maleated SEBS (Kraton MD6684CS) has made it possible to overcome these problems and create TPE compounds with improved compression set values at the same elevated temperatures (typically <40% at 700C and <65% at 1000C). A commercial example of a high molecular weight maleated SEBS ("HMW MAH-g-SEBS"), Kraton MD6684CS, has a weight average molecular weight of about 250,000. Therefore, for purposes of this invention, "high molecular weight" for maleated SEBS means a weight average molecular weight of at least about 200,000. Desirably, the "high molecular weight" is at least about 225,000, and preferably at least about 250,000. [00015] Typically, commercial grades of TPE-S are a complex combination of TPE, compatibilizer, plasticizer, processing aid, filler, antioxidant, antiblocking agent, and one or more secondary polymers. IΘ0016] The present invention replaces the LMW MAH-g-SEBS with a
HMW MAH-g-SEBS serving as a compatibilizer and introduces a secondary polymer, preferably PA which assists in compatibilization. [00017J Non-limiting examples of TPE-S include styrene-ethylene- butylene-styrene, styrene-ethylene-propylene-styrene, styrene-ethylene- ethylene/propylene-styrene, styrene-isobutylene-styrene, styrene-butadiene- styrene, styrene-isoprene-styrene, and combinations thereof. These examples of TPE-S are not maleated but have weight average molecular weights in excess of 100.000 and preferably in excess of 200,000. Commercially available grades of these TPE-S compounds are Kraton Gl 651 and Kraton MD 6933 from Kraton Polymers and Septon 4077 and Septon 4099 from Kuraray. [00018] An example of HMW MAH-g-SEBS is Kraton MD6684CS.
[00019] The replacement of LMW MAH-g-SEBS with HMW MAH-g-
SEBS is also applicable to other types of TPEs, among them thermoplastic
vulcanizates (TPVs), thermoplastic polyurethanes (TPUs), and thermoplastic olefins (TPOs), except that the TPE portion of the high molecular weight compatibilizer will need to be adjusted, as needed, to be compatible with the type of TPE employed.
[00020] Other Ingredients
[00Θ21] Any conventional plasticizer, preferably a paraffinic oil, is suitable for use the present invention.
[0ΘΘ22] A preferred processing aid is a hydrocarbon resin, preferably a rosin ester, because it improves process ability of the compound within the mixing vessel, a particular problem with high molecular weight TPEs.
[00023] A preferred secondary polymer for the present invention is polyamide, as mentioned above, because the polyamide promotes adhesion to polyamide-containing other component of the two-part component molded or extruded article.
[00024] Optional Additives
[00025] The compound of the present invention can include conventional plastics additives in an amount that is sufficient to obtain a desired processing or performance property for the compound. The amount should not be wasteful of the additive nor detrimental to the processing or performance of the compound. Those skilled in the art of thermoplastics compounding, without undue experimentation but with reference to such treatises as Plastics Additives
Database (2004) from Plastics Design Library (www.williamandrew.com), can select from many different types of additives for inclusion into the compounds of the present invention.
[00026] Non-limiting examples of optional additives include adhesion promoters; biocides (antibacterials, fungicides, and mildewcides), anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppresants; impact modifiers; initiators; lubricants; micas; pigments, colorants and dyes; plasticizers; processing aids; release agents; silanes, titanates and zirconates;
slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; and combinations of them.
[00027] Table 1 shows the acceptable, desirable, and preferable ranges of ingredients for the TPE of the present invention.
"•Though not necessarily cost-effective, one can use the HMW MAH-g-SEBS as the TPE of the present invention.
[00028] Processing
[00029] The preparation of compounds of the present invention is uncomplicated. The compound of the present can be made in batch or continuous operations.
[00030] Mixing in a continuous process typically occurs in an extruder that is elevated to a temperature that is sufficient to melt the polymer matrix with addition of all additives at the feed-throat, or by injection or side-feeders downstream. Extruder speeds can range from about 50 to about 500 revolutions per minute (rpm), and preferably from about 100 to about 300 ipm.
Typically, the output from the extruder is pelletized for later extrusion or molding into polymeric articles.
|00031] Mixing in a batch process typically occurs in a Banbury mixer that is also elevated to a temperature that is sufficient to melt the polymer matrix to permit homogenizatϊon of the compound components. The mixing speeds range from 60 to 1000 rpm and temperature of mixing can be ambient. Also, the output from the mixer is chopped into smaller sizes for later extrusion or molding into polymeric articles.
[00032] Subsequent extrusion or molding techniques are well known to those skilled in the art of thermoplastics polymer engineering. Without undue experimentation but with such references as "Extrusion, The Definitive Processing Guide and Handbook"; "Handbook of Molded Part Shrinkage and Warpage"; "Specialized Molding Techniques"; "Rotational Molding Technology"; and "Handbook of Mold, Tool and Die Repair Welding", all published by Plastics Design Library (www.williamandrew.com), one can make articles of any conceivable shape and appearance using compounds of the present invention.
USEFULNESS OF THE INVENTION
[00033] TPE-S of the present invention is an excellent one part of a two- part component polymer structure because it has excellent adhesion to polyamides including polyamide 6, polyamide 66, polyamide 11, polyamide 12 and others, which is often used as the more rigid part of the structure. In addition to door seals for automobiles, two-part component polymer structures are used in the following industrial and consumer products: power tool grips, integrated seals and gaskets, anti- vibration mounts, automotive interior trim, sound deadening parts, glazing gaskets, flexible membranes, and other articles now or hereafter known.
EXAMPLES
[00034] Table 2 shows five examples of the present invention, in comparison with a control (Comparative Example A) representing a traditional TPE-S that is commercially available.
[00035} Table 3 shows the commercial sources for the ingredients of
Table 1, with weight average molecular weight values, as applicable.
[00037] The interchangeability between types of TPE (SEEPS vs. SEBS) is attributable to their similar molecular weights.
[00038] The difference between processing aids (hydrocarbon resin vs. alpha-m ethyl styrene) is attributed to the desire to the higher melting point and therefore higher service temperature, the greater effect on viscosity and the reduced odor imparted upon the compound.
[ΘΘ039] The addition of MAH-g-PP is attributed to a desire to modify the hardness of the compound without impairing the adhesive nature (which would be affected by non-grafted PP).
[00040] The difference in compatibilizer (HMW MAH-g-SEBS vs.
LMW MAH-g-SEBS) is attributed to a desire to the improved performance at elevated temperatures of HMW MAH-g-SEBS.
[00041] All of Examples 1-5 and Comparative Example A were made using a Werner and Pfleiderer twin-screw extruder set at 2500C in all zones, rotating at 250 rpm. All ingredients were added at Zone 1 , except for the oil which was added at the injection port. The melt-mixed compound was pelletized for further handling.
[00042] Pellets of all Examples 1-5 and Comparative Example A were molded into tensile test bars using a Demag injection molding machine, operating at 180-2Q0°C temperature and medium-high pressure. [0Θ043] Table 4 shows the experimental results.
[00Θ44] For the adhesion tests, the following test method was used.
Using the Demag injection moulding machine with dual barrels, polyamide was
injected first into a custom designed tool with a moving core, after which the TPE compound was injected directly onto the polyamide. The two-component ("2K") test bars were ejected and conditioned at room temperature for 24 hours. After conditioning, an attempt was made by hand to remove the TPE strip from the polyamide substrate, and the difficulty noted. Additionally it was noted whether the bond failed by adhesive failure (where the TPE is cleanly removed from the substrate) or by cohesive failure (where a layer of TPE remains on the substrate, the interfacial strength is higher than the cohesive strength of the TPE, the optimal case).
[00045] Examples 1-5 exhibit a variety of hardnesses as well as excellent adhesion to both polyamide 6 and polyamide 6,6, two of the most popular grades of polyamide. Comparative Example A only adheres well to polyamide 6.
[00046] Even more significant is the vast improvement in compression set, seen by reviewing percent improvement of each of Examples 1-5 to Comparative Example A. At 700C, there was at least a 50% improvement in compression set. At 1000C, there was at least a 30% improvement in compression set. In practical polymer science and engineering, these improvements in compression set mean that these compounds can maintain a better seal at elevated temperatures than their predecessors, and it indicates a better performance in general at elevated temperatures. [00047] The invention is not limited to the above embodiments. The claims follow.
Claims
1. A thermoplastic elastomer compound, comprising:
(a) high molecular weight maleated styrene-ethylene-butylene-styrene;
(b) plasticizer;
(c) processing aid; and
(d) polyamide.
2. The compound of Claim 1 , further comprising styrene- containing thermoplastic elastomer.
3. The compound of Claim 1 or Claim 2, wherein the high molecular weight maleated styrene-ethylene-butylene-styrene has a weight average molecular weight of at least 200,000.
4. The compound of Claim 2 or Claim 3, wherein the stymie-containing thermoplastic elastomer is selected from the group consisting of styrene- ethylene-butylene-styrcne, styrene-ethylene-propylene-styrene, styrene- ethyϊene-ethylene/propylene-styrene, styrene-isobutylene-styrene, styrene- butadiene-styrene, styrene-isoprene-styrene, and combinations thereof.
5. The compound of any of Claims 2-4, wherein the styrene-containing thermoplastic elastomer is not maleated but has a weight average molecular weight in excess of 100,000.
6. The compound of any of Claims 1-5, wherein the plasticizer is a paraffmic oil.
7. The compound of any of Claims 1 -6, wherein the processing aid is a hydrocarbon resin.
8. The compound of any of Claims 1-8, further comprising adhesion promoters; biocides; anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers and extenders; fire and flame retardants and smoke suppressants; impact modifiers; initiators; lubricants; micas; pigments, colorants and dyes; plasticizers; additional processing aids; release agents; silanes, titanates and zirconates; slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; and combinations of them.
9. The compound of any of Claims 1-8, wherein the weight percents of the ingredients comprise:
10. A two-component article, comprising the compound of any of Claims 2- 9 as one component and polyamide as the second component.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07783855A EP2021410B1 (en) | 2006-05-30 | 2007-05-17 | Thermoplastic elastomers for adhesion to polyamide |
| AT07783855T ATE530602T1 (en) | 2006-05-30 | 2007-05-17 | THERMOPLASTIC ELASTOMERS FOR ADHESION TO A POLYAMIDE |
| US12/301,998 US8193273B2 (en) | 2006-05-30 | 2007-05-17 | Thermoplastic elastomers for adhesion to polyamide |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80344906P | 2006-05-30 | 2006-05-30 | |
| US60/803,449 | 2006-05-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2007140127A1 true WO2007140127A1 (en) | 2007-12-06 |
Family
ID=38778990
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2007/069097 WO2007140127A1 (en) | 2006-05-30 | 2007-05-17 | Thermoplastic elastomers for adhesion to polyamide |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US8193273B2 (en) |
| EP (1) | EP2021410B1 (en) |
| AT (1) | ATE530602T1 (en) |
| WO (1) | WO2007140127A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010099056A3 (en) * | 2009-02-27 | 2011-01-27 | Polyone Corporation | Biorenewable thermoplastic elastomers |
| US11827787B2 (en) | 2018-12-20 | 2023-11-28 | Actega Ds Gmbh | Thermoplastic elastomer composition |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8981003B2 (en) | 2010-03-17 | 2015-03-17 | Polyone Corporation | Biorenewable copolyester thermoplastic elastomers |
| CN103748173B (en) * | 2011-05-31 | 2017-09-22 | 普立万公司 | By thermomechanically acting on the thermoplastic elastomer compound with shape memory |
| DE102014007211A1 (en) | 2014-05-19 | 2015-11-19 | Kraiburg Tpe Gmbh & Co. Kg | Thermoplastic elastomer compositions with adhesion to metallic surfaces |
| DE102015007200A1 (en) | 2015-05-26 | 2016-12-01 | Kraiburg Tpe Gmbh & Co. Kg | Hardness adjustment of thermoplastic elastomer compositions by combination of thermoplastics and thermoplastic elastomers |
| WO2017088168A1 (en) | 2015-11-27 | 2017-06-01 | Dow Global Technologies Llc | Adhesive formulations for fabric/poe adhesion |
| WO2018234377A1 (en) | 2017-06-21 | 2018-12-27 | Basf Se | Thermoplastic polyurethane elastomer for adhesion to polyamide |
| CN108034239A (en) * | 2017-12-06 | 2018-05-15 | 常州鼎众冷暖设备工程有限公司 | One kind prevents old type heat insulating strip |
| EP3670591B1 (en) * | 2018-12-06 | 2024-10-02 | TSRC Corporation | Polymer composition, foam and method thereof |
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- 2007-05-17 WO PCT/US2007/069097 patent/WO2007140127A1/en active Application Filing
- 2007-05-17 EP EP07783855A patent/EP2021410B1/en active Active
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| US11827787B2 (en) | 2018-12-20 | 2023-11-28 | Actega Ds Gmbh | Thermoplastic elastomer composition |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2021410B1 (en) | 2011-10-26 |
| US8193273B2 (en) | 2012-06-05 |
| EP2021410A1 (en) | 2009-02-11 |
| ATE530602T1 (en) | 2011-11-15 |
| US20100227967A1 (en) | 2010-09-09 |
| EP2021410A4 (en) | 2010-06-23 |
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