GB2262941A - Oiled polymer, process for the production therof and adhesive composition comprising it - Google Patents

Oiled polymer, process for the production therof and adhesive composition comprising it Download PDF

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Publication number
GB2262941A
GB2262941A GB9227066A GB9227066A GB2262941A GB 2262941 A GB2262941 A GB 2262941A GB 9227066 A GB9227066 A GB 9227066A GB 9227066 A GB9227066 A GB 9227066A GB 2262941 A GB2262941 A GB 2262941A
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United Kingdom
Prior art keywords
oil
polymer
oiled
sis
phr
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GB9227066D0 (en
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Steven Soohyun Chin
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Shell Internationale Research Maatschappij BV
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Shell Internationale Research Maatschappij BV
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Publication of GB9227066D0 publication Critical patent/GB9227066D0/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J153/00Adhesives 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
    • C09J153/02Vinyl aromatic monomers and conjugated dienes
    • C09J153/025Vinyl aromatic monomers and conjugated dienes modified
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition 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
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

An oiled polymer composes a styrene-isoprene-styrene block copolymer and up to 50 phr of oil. An adhesive composition comprises the oiled polymer with, as the oil, a mineral oil, napthenic oil, paraffinic oil or low softening point tackifying resin. The compositions are made batch mixing the oil and polymer or by polymerizing neat 515 block copolymer in a solvent, adding the oil, and then removing the solvent.

Description

OILED POLYMER, PROCESS FOR THE PRODUCTION THEREOF AND ADHESIVE COMPOSITION COMPRISING IT Adhesive compositions are very well known. Generally, these compositions comprise 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 either 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 styreneisoprene-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 copolymers 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 up to 50 phr (parts by weight per 100 parts by weight of block copolymer) of oil, preferably 5 to 50 phr.
This invention further provides processes for producing the inventive oiled styrene-isoprene-styrene (SIS) based copolymer.
These processes include a solvent process as well as non-solvent processes, wherein oil and neat SIS block copolymer are pre-mixed 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 up to 50 phr 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 sytrenic 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 a-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 as KRATON or CARIFLEX thermoplastic polymers (KRATON and CARIFLEX are Trade Marks). A more detailed description of these types of polymers can be found, for example, in U.S. Patent No. 3,935,338; particularly from col. 2, line 52 to col. 3, line 24.
Particularly preferred among the block copolymers are the styrenic block copolymers commonly referred to as SBS (styrenebutadiene-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 centre 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 from 10,000 to 30,000 and the A-blocks constitute from 8 to 40 and preferably from 12 to 30 percent by weight of the block copolymer. Commercial products of SIS block copolymers include KRATON D-1107 (or CARIFLEX TR-1107), KRATON D-llll and D-1125. CARIFLEX TR-1107 or KRATON D-1107 is well known and is described in U.S. Patent No. 3,932,328. KRATON D-llll generally comprises 20 to 24 percent by weight of the A block and has a solution viscosity of 1300 centipoise at 25% wt solids in toluene at room temperature. KRATON D-1125 generally comprises 28 to 32 percent by weight of the A block and the polymer possesses a solution viscosity of 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. Patent No. 4,286,077.
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 (Tufflo is a Trade Mark) and mineral oils such as Kaydol (Kaydol is a Trade Mark) are preferred for long term melt and colour stability of the adhesive.
Naphthenic oils with low aromatic content such as SHELLFLEX 371 (SHELLFLEX is a Trade Mark) 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, such as those described in col. 3, lines 15 to 49 of U.S. Patent No. 4,728,572. 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 process comprises the steps of: (a) polymerizing neat SIS block copolymer in a solvent; (b) adding from 5 to 50 parts of oil to said SIS block copolymer and to form the oiled polymer; (c) removing the solvent from the oiled polymer.
In a second embodiment, the process comprises 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.
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 5 to 50 phr. A preferred amount of oil in the polymer is from 10 to 30 phr.
The oiled polymer is then used in the production of an adhesive composition. The adhesive composition can be made using any method known in the art, such as the hot melt or the solvent method. These methods are disclosed in for example, U.S. Patent No. 4,728,572.
The adhesive composition comprises 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 and may be present in amounts varying from O to 50 phr. Generally speaking though, such end-product applications and the necessary adjustments in the amounts of oil, is considered to be within the competence of a person skilled in the art.
In numeric terms, the adhesive composition generally comprises: (a) 105 to 150 pbw (parts by weight) of oiled, SIS block copolymer; (b) O to 50 pbw of oil, preferably from 10 to 60 phr; (c) 50 to 300 pbw of tackifying resin, preferably from 100-250 phr; and (d) 0.05 to 5.0 pbw of antioxidant.
The invention is further described by the following non-limiting examples.
EXAMPLE 1 An SIS polymer (KRATON D-llll) 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.
EXAMPLE 2 An SIS polymer (KRATON D-1107) 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.
EXAMPLE 3 An SIS polymer (KRATON D-1125) 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.
EXAMPLE 4 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 pbw (parts by weight) 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) Total Mix Time (Min) Minimum Maximum KRATON D-1107 22 98 11 11 phr oiled KRATON D-1107 25 99 8 KRATON D-1125 18 46 12 25 phr oiled RP-6405 32 47 8 KRATON D-llll 49 84 25 21 phr oiled KRATON D-llll 37 93 14 33 phr oiled KRATON D-llll 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 (11)

1. An oiled polymer comprising a styrene-isoprene-styrene block copolymer and up to 50 phr of oil.
2. An oiled polymer according to claim 1 comprising 5 to 50 phr of oil.
3. A polymer as in claim 2 wherein said oil is present in an amount of from 10 to 30 phr.
4. A polymer as in claims 1-3 wherein said oil is selected from the group consisting of mineral oils, naphthenic oils, paraffinic oils, and low softening point tackifying resins.
5. A polymer as in claim 4 wherein said oil is a naphthenic oil.
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 5 to 50 parts of oil to said SIS block copolymer 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 any one of claims 1 to 5 and at least one tackifying resin.
10. A composition as in claim 9 further comprising predetermined additional amounts of oil.
11. An adhesive composition according to claim 9 or 10 comprising in numeric term: (a) 105 to 150 pbw of an oiled SIS block copolymer; (b) O to 50 pbw of oil; (c) 50 to 300 pbw of tackifying resin; and (d) 0.05 to 5.0 pbw of antioxidant.
GB9227066A 1991-12-31 1992-12-29 Oiled polymer, process for the production therof and adhesive composition comprising it Withdrawn GB2262941A (en)

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US07/816,508 USH1338H (en) 1991-12-31 1991-12-31 Oiled polymer and process for the production thereof

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* Cited by examiner, † Cited by third party
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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US3954692A (en) * 1969-03-17 1976-05-04 The Goodyear Tire & Rubber Company Adhesive composition
US4097434A (en) * 1976-04-05 1978-06-27 Shell Oil Company Adhesive composition
US4587289A (en) * 1982-09-27 1986-05-06 Ahmet Comert Adhesive thermoplastic compositions
US4728572A (en) * 1986-04-14 1988-03-01 National Starch And Chemical Corp. Removable hot melt pressure sensitive adhesive
US5019071A (en) * 1989-12-12 1991-05-28 Minnesota Mining And Manufacturing Company Adhesive fastening tab
EP0443263A2 (en) * 1990-02-22 1991-08-28 Minnesota Mining And Manufacturing Company Repositionable adhesive tape

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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
US3992339A (en) 1975-05-15 1976-11-16 Shell Oil Company Primers for use between metal substrates and block copolymers
CA1066830A (en) 1976-01-07 1979-11-20 Ronald J. Tabar Sacrificial binders for molding particulate solids and the molding thereof
US4286077A (en) 1980-04-21 1981-08-25 Shell Oil Company Weather resistant adhesive composition
US4500021A (en) 1980-12-24 1985-02-19 Eschem, Inc. Resealable articles and process
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US4419494A (en) 1982-03-16 1983-12-06 National Starch And Chemical Corporation Heat resistant hot melt adhesives
US4551490A (en) 1983-06-27 1985-11-05 E. R. Squibb & Sons, Inc. Adhesive composition resistant to biological fluids
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EP0234615A1 (en) 1986-02-28 1987-09-02 Shell Internationale Researchmaatschappij B.V. Process for the preparation of bituminous compositions contaning block copolymers
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Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3954692A (en) * 1969-03-17 1976-05-04 The Goodyear Tire & Rubber Company Adhesive composition
US3935338A (en) * 1973-04-23 1976-01-27 Shell Oil Company Process for the preparation of pressure-sensitive adhesive articles
US4097434A (en) * 1976-04-05 1978-06-27 Shell Oil Company Adhesive composition
US4587289A (en) * 1982-09-27 1986-05-06 Ahmet Comert Adhesive thermoplastic compositions
US4728572A (en) * 1986-04-14 1988-03-01 National Starch And Chemical Corp. Removable hot melt pressure sensitive adhesive
US5019071A (en) * 1989-12-12 1991-05-28 Minnesota Mining And Manufacturing Company Adhesive fastening tab
EP0443263A2 (en) * 1990-02-22 1991-08-28 Minnesota Mining And Manufacturing Company Repositionable adhesive tape

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USH1338H (en) 1994-07-05
GB9227066D0 (en) 1993-02-24

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