USH1338H - Oiled polymer and process for the production thereof - Google Patents
Oiled polymer and process for the production thereof Download PDFInfo
- Publication number
- USH1338H USH1338H US07/816,508 US81650891A USH1338H US H1338 H USH1338 H US H1338H US 81650891 A US81650891 A US 81650891A US H1338 H USH1338 H US H1338H
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- US
- United States
- Prior art keywords
- polymer
- oil
- oiled
- styrene
- block copolymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 229920000642 polymer Polymers 0.000 title claims abstract description 59
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title abstract description 19
- 239000000853 adhesive Substances 0.000 claims abstract description 31
- 230000001070 adhesive effect Effects 0.000 claims abstract description 31
- 239000000203 mixture Substances 0.000 claims abstract description 25
- 239000003921 oil Substances 0.000 claims description 45
- 239000002904 solvent Substances 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 13
- 229920005989 resin Polymers 0.000 claims description 13
- 229920001400 block copolymer Polymers 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 239000002480 mineral oil Substances 0.000 claims description 3
- 239000010690 paraffinic oil Substances 0.000 claims description 3
- 238000013329 compounding Methods 0.000 claims description 2
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 claims 8
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 abstract description 5
- 238000006731 degradation reaction Methods 0.000 abstract description 5
- 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 description 25
- 229920002633 Kraton (polymer) Polymers 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 6
- 229920006132 styrene block copolymer Polymers 0.000 description 5
- 239000012943 hotmelt Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 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 description 3
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 229920002725 thermoplastic elastomer Polymers 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000010128 melt processing Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- -1 styrene-ethylene-butylene-styrene Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J153/02—Vinyl aromatic monomers and conjugated dienes
- C09J153/025—Vinyl aromatic monomers and conjugated dienes modified
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
Definitions
- Adhesive compositions are very well known. Generally, these compositions comprise of a thermoplastic elastomer, such as a styrenic block copolymer, a tackifying resin and a processing oil. Adhesives are generally produced either by dissolving all the ingredients in a common solvent capable of dissolving all the ingredients or by a hot melt process where the ingredients are melt processed at an elevated temperature.
- the polymer, tackifying resin and oil can be added as separate ingredients or the polymer and oil can be premixed then added together with the resin.
- the polymer is referred to as a neat or unoiled polymer.
- a common problem is that the neat polymer is difficult to mix, resulting in longer mixing times. Long mixing times is a disadvantage in the production of adhesives whether from solvent or hot melt process. In hot melt mixes in particular, if the mixing time is long the copolymer degrades during melt processing to generate lower molecular weight species. This degradation occurs due to the presence of oxygen, and due to shear degradation of the high viscosity copolymers. If the resulting degradation is severe, the resulting adhesive is no longer useful for the intended application.
- This invention provides an oiled styrene-isoprene-styrene (SIS) based copolymer comprising from about 5 to 50 parts of oil.
- SIS oiled styrene-isoprene-styrene
- This invention further provides processes for producing the inventive oiled styrene-isoprene-styrene (SIS) based copolymer.
- processes include a solvent process, and non-solvent processes wherein oil and neat SIS block copolymer are premixed or are added separately into a batch or continuous mixer.
- the invention also provides an adhesive composition comprising a tackifying resin and an oiled styrene-isoprene-styrene (SIS) based block copolymer comprising from about 5 to 50 parts of oil.
- SIS oiled styrene-isoprene-styrene
- predetermined additional amounts of oil can be added to the adhesive composition.
- the advantages of the inventive processes include a reduction in mixing time which reduces the amount of time the styrenic block copolymer in the adhesive is exposed to the thermo-oxidative environment thereby reducing polymer degradation. Also, the presence of oil in the polymer reduces shear degradation during melt processing.
- the basic materials that are useful in the practice of this invention are a thermoplastic elastomer, an oil, and a tackifying resin.
- Thermoplastic elastomers useful herein include those based on poly ⁇ -olefins, polyesteramides, polyether, polyurethane, polystyrene, polybutadiene, and polyisoprene.
- block copolymers comprising of homopolymers or copolymers of conjugated dienes or copolymers of one or more conjugated dienes and one or more monoalkenyl aromatic hydrocarbons.
- These block copolymers are manufactured and sold by Shell Chemical Company as KRATON® thermoplastic polymers. A more detailed description of these types of polymers can be found, for example, in U.S. Pat. No. 3,935,338; particularly from col. 2, line 52 to col. 3, line 24. The disclosure of this patent is herein incorporated by reference.
- block copolymers particularly preferred among the block copolymers are the styrenic block copolymers commonly referred to as SBS (styrene-butadiene-styrene), SIS (styrene-isoprene-styrene), and SEBS (styrene-ethylene-butylene-styrene). Most particularly preferred are the SIS copolymers.
- SIS block copolymers comprise an elastomeric center block derived from isoprene, i.e. polymerized from isoprene either alone or in conjunction with a small proportion of other monomers; and thermoplastic A-blocks (end-blocks) derived from styrene, i.e. polymerized from styrene or styrene homologues.
- the individual A-blocks have a number average molecular weight of at least 7,000 preferably in the range of about 10,000 to 30,000 and the A-blocks constitute from about 8 to 40 and preferably about 12 to 30 percent by weight of the block copolymer.
- Commercial products of SIS block copolymers include KRATON® 1107, 1111, AND 1125.
- KRATON® 1107 is well known and is described in U.S. Pat. No. 3,932,328.
- KRATON® D1111 generally comprises about 20 to 24 percent by weight of the A block and has a solution viscosity of about 1300 centipoise at 25% wt solids in toluene at room temperature.
- KRATON® D1125 generally comprises about 28 to 32 percent by weight of the A block and the polymer possesses a solution viscosity of about 300 centipoise at 25% wt. solids in toluene at room temperature.
- compositions comprising oiled SBS and SEBS are known. Because of the aforementioned problems, oiled SIS polymer has not been used to produce adhesive compositions.
- oils are useful in the practice of this invention. More specifically, oils that are particularly useful herein are those that are used as plasticizers in adhesives based on styrenic block copolymers. Such oils have a solubility parameter close to that of the rubber block, in this case isoprene, and have a high molecular weight to minimize compatibility with the polystyrene endblock phase.
- oils are exemplified by aromatic oils, mineral oils, naphthenic oils, paraffinic oils, and low softening point tackifying resins.
- Naphthenic oils are more compatible with SIS polymers than paraffinic oils. More highly refined aromatic-free "white oils” such as Tufflo 6056 a tradename of ARCO and mineral oils such as Kaydol a tradename of Witco are preferred for long term melt and color stability of the adhesive.
- Naphthenic oils with low aromatic content such as SHELLFLEX® 371 (a trademark of Shell Chemical Company) which combine the characteristics of high compatibility, affecting plasticizing and low cost are ideally suited for use with styrenic block copolymers such as SIS polymers.
- compositions of this invention may also contain additional materials including antioxidants, fillers, pigments, and the like.
- Antioxidants useful herein include phenolic and secondary antioxidants. A representative listing of those antioxidants can be found at col. 3, lines 15 to 49 of U.S. Pat. No. 4,728,572 which is herein incorporated by reference. Fillers, pigments, and like materials that are conventionally used and known in the art are likewise useful in the practice of this invention.
- the polymer is made in solvent, then oil is added to the solvent, and the solvent is subsequently removed using art-known conventional devices.
- the oil and polymer can be premixed and then metered into a continuous or batch mixer for compounding.
- the oil and polymer can be added separately into the batch or continuous mixer.
- any of the solvents known in the prior art to be useful in the preparation of adhesives may be used as the solvent in the first embodiment.
- Such a solvent is one that is capable of dissolving all of the ingredients of the adhesive and evaporating after the adhesive is completely formulated.
- Suitable solvents having this characteristic include straight- and branched-chain hydrocarbons such as pentane, hexane, heptane, octane and the like, as well as alkyl-substituted derivatives thereof: cycloaliphatic hydrocarbons such as cyclopentane, cyclohexane, cycloheptane and the like, as well as alkyl-substituted derivatives thereof; aromatic and alkyl-substituted aromatic hydrocarbons such as benzene, toluene, xylene and the like; hydrogenated aromatic hydrocarbons, such as tetralin, decalin and the like.
- Linear and cyclic ethers such as dimethyl ether, methyl ethyl ether, tetrahydrofuran and the like may be used in small amounts.
- the amount of oil that is incorporated into the polymer is generally within the range of from about 5 to 50 parts.
- a preferred amount of oil in the polymer is from about 10 to 30 parts.
- the oiled polymer is then used in the production of an adhesive composition.
- the adhesive composition can be made using any art-known method such as the hot melt or the solvent method. These methods are disclosed in for example, U.S. Pat. No. 4,728,572 which is herein incorporated by reference.
- the adhesive composition comprises of a tackifying resin, an oiled polymer comprising a predetermined amount of oil, and conventional additives such as antioxidants. It is to be noted that for some applications, the adhesive composition may be required to contain more oil than is present in the oiled polymer. In such instances, additional oil will be added during the production of the adhesive composition. Generally speaking though, such end-product applications and the necessary adjustments in the amounts of oil, is considered to be within the competence of one skilled in the art.
- the adhesive composition generally comprises:
- For the oil from about 5 to 100, preferably from 10 to 60 parts;
- tackifying resin from about 50-300, preferably from 100-250 parts;
- For the antioxidant from about 0.05 to 2.0 parts.
- SIS polymer (KRATON® D1111) was anionically polymerized using cyclohexane as solvent. After the completion of anionic polymerization, 33 phr of SHELLFLEX® 371 oil was metered into the solvent/polymer blend and thoroughly mixed. After mixing, the solvent was removed by melt devolatilization to produce dense pellets of SIS oiled polymers.
- An SIS polymer (KRATON® D1107) was polymerized using the method of Example 1.
- the polymer and 11 phr of SHELLFLEX® 371 oil were dry blended together in a Henschel mixer. After 10 minutes of mixing in the Henschel mixer, the dry blend was fed into a twin screw extruder for further mixing and pelletization. The mixing and exit temperatures at the extruder were 180° C. and 200° C., respectively.
- the pellets formed contained SIS oiled polymer.
- An SIS polymer (KRATON® D1125) was polymerized using the method of Example 1. The polymer was fed directly into the throat of a twin screw extruder and 25 phr of SHELLFLEX® 371 oil was injected directly into the extruder. After melt mixing in the twin screw extruder, the oiled polymer was pelletized to form dense pellets.
- Table 1 compares the torque and mixing times of adhesive produced from neat, unoiled polymers to those produced from oiled polymers where the final adhesive composition was 100 phr SIS polymer, 187 phr 105° C. softening point hydrogenated tackifying resin (Escorez 5300), 47 phr oil (SHELLFLEX® 371), and 3 phr phenolic antioxidant (Irganox 1010). Mixing was conducted on a Brabender Prep Mixer with a 250 cc mixing capacity.
- the Prep mixer was equipped with a torque rheometer capable of determining the mixing torque as a function of mix time.
- the total mix time was determined as the time between initial softening of ingredients (fluxing) which is indicated by the minimum torque and the maximum torque when mixing is complete.
- the mixer temperature was set at 195° C. and the adhesive mix temperature ranged from 135° C. at initial softening or "fluxing" of ingredients to a final adhesive mix temperature of 180° C.
- the total mixing time for the adhesives made with the inventive oiled polymers is reduced by as much as 50%.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Oiled SIS polymers and processes for their production are disclosed. These processes result in advantages including reduced mixing time and less shear degradation. An adhesive composition comprising the oiled polymer of the invention is also disclosed.
Description
Adhesive compositions are very well known. Generally, these compositions comprise of a thermoplastic elastomer, such as a styrenic block copolymer, a tackifying resin and a processing oil. Adhesives are generally produced either by dissolving all the ingredients in a common solvent capable of dissolving all the ingredients or by a hot melt process where the ingredients are melt processed at an elevated temperature.
During the production of adhesives, the polymer, tackifying resin and oil can be added as separate ingredients or the polymer and oil can be premixed then added together with the resin. When separate addition is utilized, the polymer is referred to as a neat or unoiled polymer. A common problem is that the neat polymer is difficult to mix, resulting in longer mixing times. Long mixing times is a disadvantage in the production of adhesives whether from solvent or hot melt process. In hot melt mixes in particular, if the mixing time is long the copolymer degrades during melt processing to generate lower molecular weight species. This degradation occurs due to the presence of oxygen, and due to shear degradation of the high viscosity copolymers. If the resulting degradation is severe, the resulting adhesive is no longer useful for the intended application.
Presoaking the polymer in oil or premixing the oil and polymer prior to their use in producing adhesives are alternative methods which are known in the art. However, these methods have not been utilized in the production of adhesives based on styrene-isoprene-styrene (SIS) block copolymer. One reason for this is that SIS block copolymers are too soft for handling. Thus, addition of oil prior to processing makes these block copolymer excessively tacky. Another reason is that with presoaking, an extra step is involved or required.
Thus, there continues to exist a need for improved methods of processing oiled SIS polymers in order to facilitate the production of good quality SIS polymer based adhesive compositions.
This invention provides an oiled styrene-isoprene-styrene (SIS) based copolymer comprising from about 5 to 50 parts of oil.
This invention further provides processes for producing the inventive oiled styrene-isoprene-styrene (SIS) based copolymer. These processes include a solvent process, and non-solvent processes wherein oil and neat SIS block copolymer are premixed or are added separately into a batch or continuous mixer.
The invention also provides an adhesive composition comprising a tackifying resin and an oiled styrene-isoprene-styrene (SIS) based block copolymer comprising from about 5 to 50 parts of oil. Optionally, depending on its intended application(s), predetermined additional amounts of oil can be added to the adhesive composition.
The advantages of the inventive processes include a reduction in mixing time which reduces the amount of time the styrenic block copolymer in the adhesive is exposed to the thermo-oxidative environment thereby reducing polymer degradation. Also, the presence of oil in the polymer reduces shear degradation during melt processing.
In very general terms, the basic materials that are useful in the practice of this invention are a thermoplastic elastomer, an oil, and a tackifying resin.
Thermoplastic elastomers useful herein include those based on poly α-olefins, polyesteramides, polyether, polyurethane, polystyrene, polybutadiene, and polyisoprene.
Preferred among this group are block copolymers comprising of homopolymers or copolymers of conjugated dienes or copolymers of one or more conjugated dienes and one or more monoalkenyl aromatic hydrocarbons. These block copolymers are manufactured and sold by Shell Chemical Company as KRATON® thermoplastic polymers. A more detailed description of these types of polymers can be found, for example, in U.S. Pat. No. 3,935,338; particularly from col. 2, line 52 to col. 3, line 24. The disclosure of this patent is herein incorporated by reference.
Particularly preferred among the block copolymers are the styrenic block copolymers commonly referred to as SBS (styrene-butadiene-styrene), SIS (styrene-isoprene-styrene), and SEBS (styrene-ethylene-butylene-styrene). Most particularly preferred are the SIS copolymers.
These SIS block copolymers comprise an elastomeric center block derived from isoprene, i.e. polymerized from isoprene either alone or in conjunction with a small proportion of other monomers; and thermoplastic A-blocks (end-blocks) derived from styrene, i.e. polymerized from styrene or styrene homologues. The individual A-blocks have a number average molecular weight of at least 7,000 preferably in the range of about 10,000 to 30,000 and the A-blocks constitute from about 8 to 40 and preferably about 12 to 30 percent by weight of the block copolymer. Commercial products of SIS block copolymers include KRATON® 1107, 1111, AND 1125. KRATON® 1107 is well known and is described in U.S. Pat. No. 3,932,328. KRATON® D1111 generally comprises about 20 to 24 percent by weight of the A block and has a solution viscosity of about 1300 centipoise at 25% wt solids in toluene at room temperature. KRATON® D1125 generally comprises about 28 to 32 percent by weight of the A block and the polymer possesses a solution viscosity of about 300 centipoise at 25% wt. solids in toluene at room temperature.
Commercial compositions comprising oiled SBS and SEBS are known. Because of the aforementioned problems, oiled SIS polymer has not been used to produce adhesive compositions.
Generally speaking, all tackifying resins useful in adhesive compositions are suitable in the practice of this invention. An exemplary listing of such tackifying resins can be found at Col. 4, lines 18-37 of U.S. Pat. No. 4,286,077 which is herein incorporated by reference.
Very broadly speaking, all oils are useful in the practice of this invention. More specifically, oils that are particularly useful herein are those that are used as plasticizers in adhesives based on styrenic block copolymers. Such oils have a solubility parameter close to that of the rubber block, in this case isoprene, and have a high molecular weight to minimize compatibility with the polystyrene endblock phase.
These oils are exemplified by aromatic oils, mineral oils, naphthenic oils, paraffinic oils, and low softening point tackifying resins. Naphthenic oils are more compatible with SIS polymers than paraffinic oils. More highly refined aromatic-free "white oils" such as Tufflo 6056 a tradename of ARCO and mineral oils such as Kaydol a tradename of Witco are preferred for long term melt and color stability of the adhesive. Naphthenic oils with low aromatic content such as SHELLFLEX® 371 (a trademark of Shell Chemical Company) which combine the characteristics of high compatibility, affecting plasticizing and low cost are ideally suited for use with styrenic block copolymers such as SIS polymers.
The compositions of this invention may also contain additional materials including antioxidants, fillers, pigments, and the like. Antioxidants useful herein include phenolic and secondary antioxidants. A representative listing of those antioxidants can be found at col. 3, lines 15 to 49 of U.S. Pat. No. 4,728,572 which is herein incorporated by reference. Fillers, pigments, and like materials that are conventionally used and known in the art are likewise useful in the practice of this invention.
There are, at least, three different embodiments of the process of making the oiled polymer component of this invention. In one embodiment, the polymer is made in solvent, then oil is added to the solvent, and the solvent is subsequently removed using art-known conventional devices. In a second embodiment, the oil and polymer can be premixed and then metered into a continuous or batch mixer for compounding. In a third embodiment, the oil and polymer can be added separately into the batch or continuous mixer.
In general, any of the solvents known in the prior art to be useful in the preparation of adhesives may be used as the solvent in the first embodiment. Such a solvent is one that is capable of dissolving all of the ingredients of the adhesive and evaporating after the adhesive is completely formulated. Suitable solvents having this characteristic include straight- and branched-chain hydrocarbons such as pentane, hexane, heptane, octane and the like, as well as alkyl-substituted derivatives thereof: cycloaliphatic hydrocarbons such as cyclopentane, cyclohexane, cycloheptane and the like, as well as alkyl-substituted derivatives thereof; aromatic and alkyl-substituted aromatic hydrocarbons such as benzene, toluene, xylene and the like; hydrogenated aromatic hydrocarbons, such as tetralin, decalin and the like. Linear and cyclic ethers such as dimethyl ether, methyl ethyl ether, tetrahydrofuran and the like may be used in small amounts.
Regardless of the method of making the oiled polymer, the amount of oil that is incorporated into the polymer is generally within the range of from about 5 to 50 parts. A preferred amount of oil in the polymer is from about 10 to 30 parts.
The oiled polymer is then used in the production of an adhesive composition. The adhesive composition can be made using any art-known method such as the hot melt or the solvent method. These methods are disclosed in for example, U.S. Pat. No. 4,728,572 which is herein incorporated by reference.
The adhesive composition comprises of a tackifying resin, an oiled polymer comprising a predetermined amount of oil, and conventional additives such as antioxidants. It is to be noted that for some applications, the adhesive composition may be required to contain more oil than is present in the oiled polymer. In such instances, additional oil will be added during the production of the adhesive composition. Generally speaking though, such end-product applications and the necessary adjustments in the amounts of oil, is considered to be within the competence of one skilled in the art.
In numeric terms, the adhesive composition generally comprises:
For the polymer about 100 parts;
For the oil, from about 5 to 100, preferably from 10 to 60 parts;
For the tackifying resin, from about 50-300, preferably from 100-250 parts; and
For the antioxidant from about 0.05 to 2.0 parts.
The invention is further described by the following non-limiting examples.
An SIS polymer (KRATON® D1111) was anionically polymerized using cyclohexane as solvent. After the completion of anionic polymerization, 33 phr of SHELLFLEX® 371 oil was metered into the solvent/polymer blend and thoroughly mixed. After mixing, the solvent was removed by melt devolatilization to produce dense pellets of SIS oiled polymers.
An SIS polymer (KRATON® D1107) was polymerized using the method of Example 1. The polymer and 11 phr of SHELLFLEX® 371 oil were dry blended together in a Henschel mixer. After 10 minutes of mixing in the Henschel mixer, the dry blend was fed into a twin screw extruder for further mixing and pelletization. The mixing and exit temperatures at the extruder were 180° C. and 200° C., respectively. The pellets formed contained SIS oiled polymer.
An SIS polymer (KRATON® D1125) was polymerized using the method of Example 1. The polymer was fed directly into the throat of a twin screw extruder and 25 phr of SHELLFLEX® 371 oil was injected directly into the extruder. After melt mixing in the twin screw extruder, the oiled polymer was pelletized to form dense pellets.
The usefulness of oiled SIS-type polymers in melt mixing is demonstrated in the reduction in total mixing time when compared to the mixing of neat, unoiled polymers. Table 1 compares the torque and mixing times of adhesive produced from neat, unoiled polymers to those produced from oiled polymers where the final adhesive composition was 100 phr SIS polymer, 187 phr 105° C. softening point hydrogenated tackifying resin (Escorez 5300), 47 phr oil (SHELLFLEX® 371), and 3 phr phenolic antioxidant (Irganox 1010). Mixing was conducted on a Brabender Prep Mixer with a 250 cc mixing capacity. The Prep mixer was equipped with a torque rheometer capable of determining the mixing torque as a function of mix time. The total mix time was determined as the time between initial softening of ingredients (fluxing) which is indicated by the minimum torque and the maximum torque when mixing is complete. The mixer temperature was set at 195° C. and the adhesive mix temperature ranged from 135° C. at initial softening or "fluxing" of ingredients to a final adhesive mix temperature of 180° C. As illustrated in Table 1, the total mixing time for the adhesives made with the inventive oiled polymers is reduced by as much as 50%.
TABLE 1
______________________________________
Mixing Time Reduction
Torque (N-m)
Maxi- Total Mix
Minimum
mum Time (Min)
______________________________________
KRATON ® D1107
22 98 11
11 phr oiled KRATON ® D1107
25 99 8
KRATON ® D1125
18 46 12
25 phr oiled RP-6405
32 47 8
KRATON ® D1111
49 84 25
21 phr oiled KRATON ® D1111
37 93 14
33 phr oiled KRATON ® D1111
43 93 12
______________________________________
While this invention has been described in detail for the purpose of illustration, it is not to be construed as limited thereby but is intended to cover all changes and modifications within the spirit and scope thereof.
Claims (14)
1. An oiled polymer comprising a styrene-isoprene-styrene block copolymer and from about 5 to 50 parts of oil.
2. A polymer as in claim 1 wherein said oil is selected from the group consisting of mineral oils, naphthenic oils, paraffinic oils, and low softening point tackifying resins.
3. A polymer as in claim 1 wherein said oil is a naphthenic oil.
4. A polymer as in claim 3 wherein said naphthenic oil is one with a low aromatic content.
5. A polymer as in claim 1 wherein said oil is present in an amount of from 10 to 30 parts.
6. A process for preparing the oiled polymer of claim 1 comprising the steps of:
(a) polymerizing neat SIS block copolymer in a solvent;
(b) adding from about 5 to 50 parts of oil to (a) and to form the oiled polymer;
(c) removing the solvent from the oiled polymer.
7. A process for preparing the oiled polymer of claim 1 comprising the steps of:
(a) premixing oil and neat SIS copolymer to form a premixed oiled polymer; and
(b) metering the product of (a) into a continuous or batch mixer for compounding.
8. A process for preparing the oiled polymer of claim 1 comprising separately adding oil and neat SIS copolymer into a batch or continuous mixer.
9. An adhesive composition comprising the oiled polymer of claim 1 and at least one tackifying resin.
10. A composition as in claim 9 further comprising predetermined additional amounts of oil.
11. A polymer as in claim 1 wherein said styrene-isoprene block copolymer is present in an amount of from about 14-32 wt %.
12. A polymer as in claim 11 wherein said styrene-isoprene block copolymer is about 15 wt %.
13. A polymer as in claim 11 wherein said styrene-isoprene block copolymer is about 21 wt %.
14. A polymer as in claim 11 wherein said styrene-isoprene block copolymer is about 30 wt %.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/816,508 USH1338H (en) | 1991-12-31 | 1991-12-31 | Oiled polymer and process for the production thereof |
| GB9227066A GB2262941A (en) | 1991-12-31 | 1992-12-29 | Oiled polymer, process for the production therof and adhesive composition comprising it |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/816,508 USH1338H (en) | 1991-12-31 | 1991-12-31 | Oiled polymer and process for the production thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH1338H true USH1338H (en) | 1994-07-05 |
Family
ID=25220827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/816,508 Abandoned USH1338H (en) | 1991-12-31 | 1991-12-31 | Oiled polymer and process for the production thereof |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | USH1338H (en) |
| GB (1) | GB2262941A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060135924A1 (en) * | 2004-12-16 | 2006-06-22 | Luizzi Joseph M | Absorbent article having a skin contactable hot melt pressure sensitive adhesive |
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|---|---|---|---|---|
| US3870676A (en) | 1973-04-23 | 1975-03-11 | Shell Oil Co | Stabilized block copolymer compositions |
| US3932328A (en) | 1971-11-02 | 1976-01-13 | Johnson & Johnson | Hot melt adhesive composition and tape |
| US3935338A (en) | 1973-04-23 | 1976-01-27 | Shell Oil Company | Process for the preparation of pressure-sensitive adhesive articles |
| US3954692A (en) | 1969-03-17 | 1976-05-04 | The Goodyear Tire & Rubber Company | Adhesive composition |
| US3992339A (en) | 1975-05-15 | 1976-11-16 | Shell Oil Company | Primers for use between metal substrates and block copolymers |
| BE850131A (en) | 1976-01-07 | 1977-05-02 | Ford Motor Co | CONSUMABLE BINDERS FOR MOLDING SOLIDS IN PARTICLES |
| US4286077A (en) | 1980-04-21 | 1981-08-25 | Shell Oil Company | Weather resistant adhesive composition |
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| US4399249A (en) | 1980-12-24 | 1983-08-16 | Eschem Inc. | Resealable pressure sensitive adhesives and products |
| US4419494A (en) | 1982-03-16 | 1983-12-06 | National Starch And Chemical Corporation | Heat resistant hot melt adhesives |
| US4500021A (en) | 1980-12-24 | 1985-02-19 | Eschem, Inc. | Resealable articles and process |
| US4551490A (en) | 1983-06-27 | 1985-11-05 | E. R. Squibb & Sons, Inc. | Adhesive composition resistant to biological fluids |
| US4619851A (en) | 1983-07-21 | 1986-10-28 | Avery International Corporation | Adhesive compositions |
| EP0234615A1 (en) | 1986-02-28 | 1987-09-02 | Shell Internationale Researchmaatschappij B.V. | Process for the preparation of bituminous compositions contaning block copolymers |
| US4728572A (en) | 1986-04-14 | 1988-03-01 | National Starch And Chemical Corp. | Removable hot melt pressure sensitive adhesive |
| US4743497A (en) | 1985-08-08 | 1988-05-10 | Phillips Petroleum Company | Laminated puncture sealing composite and preparation thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4097434A (en) * | 1976-04-05 | 1978-06-27 | Shell Oil Company | Adhesive composition |
| FR2533577B1 (en) * | 1982-09-27 | 1986-02-28 | Norton Sa | ADHESIVE THERMOPLASTIC COMPOSITIONS |
| US5019071A (en) * | 1989-12-12 | 1991-05-28 | Minnesota Mining And Manufacturing Company | Adhesive fastening tab |
| CA2032125A1 (en) * | 1990-02-22 | 1991-08-23 | John A. Miller | Repositionable adhesive tape |
-
1991
- 1991-12-31 US US07/816,508 patent/USH1338H/en not_active Abandoned
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1992
- 1992-12-29 GB GB9227066A patent/GB2262941A/en not_active Withdrawn
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|---|---|---|---|---|
| US3954692A (en) | 1969-03-17 | 1976-05-04 | The Goodyear Tire & Rubber Company | Adhesive composition |
| US3932328A (en) | 1971-11-02 | 1976-01-13 | Johnson & Johnson | Hot melt adhesive composition and tape |
| US3870676A (en) | 1973-04-23 | 1975-03-11 | Shell Oil Co | Stabilized block copolymer compositions |
| US3935338A (en) | 1973-04-23 | 1976-01-27 | Shell Oil Company | Process for the preparation of pressure-sensitive adhesive articles |
| US3992339A (en) | 1975-05-15 | 1976-11-16 | Shell Oil Company | Primers for use between metal substrates and block copolymers |
| BE850131A (en) | 1976-01-07 | 1977-05-02 | Ford Motor Co | CONSUMABLE BINDERS FOR MOLDING SOLIDS IN PARTICLES |
| US4286077A (en) | 1980-04-21 | 1981-08-25 | Shell Oil Company | Weather resistant adhesive composition |
| US4399249A (en) | 1980-12-24 | 1983-08-16 | Eschem Inc. | Resealable pressure sensitive adhesives and products |
| US4500021A (en) | 1980-12-24 | 1985-02-19 | Eschem, Inc. | Resealable articles and process |
| US4377647A (en) | 1981-11-16 | 1983-03-22 | Shell Oil Company | Polymer blend composition |
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| US4743497A (en) | 1985-08-08 | 1988-05-10 | Phillips Petroleum Company | Laminated puncture sealing composite and preparation thereof |
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| KRATON® Thermoplastic Rubber in Asphalt Products, Technical Bulletin, Shell Chem. Co., SC:57-84, Feb. 1985. |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060135924A1 (en) * | 2004-12-16 | 2006-06-22 | Luizzi Joseph M | Absorbent article having a skin contactable hot melt pressure sensitive adhesive |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2262941A (en) | 1993-07-07 |
| GB9227066D0 (en) | 1993-02-24 |
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| AS | Assignment |
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