A wide variety of pressure sensitive adhesive compositions have been available for many years. One particularly useful variety of such pressure sensitive adhesive compositions are those compositions which con¬ tain block copolymer. Such block copolymers generally are of the ABA configuration wherein the A blocks are of a polymer of relatively rigid material and the B blocks are of a polymer of a diene such as butadiene or isoprene. Such block copolymers are well known and are set forth in the following U.S. Patents: U.S. 3,239,478; U.S. 3,592,710; U.S. 3,635,861; U.S. 3,676,202; U.S. 3,723,170; U.S. 3,935,338; U.S. 4,131,709; U.S3 4,136,137; U.S. 4,178,275; U.S.

4,325,770 and German Offenlegunsschrifts 2348923 and 2736952.

Pressure sensitive adhesive compositions employing triblock polymers often are found-lacking in their abiity to withstand heat and such adhesives have a marked tendency to creep.

It would be desirable if there were available an improved pressure sensitive adhesive formulation having a greater resistance to heat and having a greater resistance to creep while providing desired adhesion.

,5 These benefits and other advantages in accor¬ dance with the present invention are achieved in a pressure sensitive adhesive composition comprising (1) a block copolymer of ABA configuration wherein the A block is a copolymer of alpha-methylstyrene and styrene 0 and the B block of the polymer is a diene polymer; and (2) a tackifying resin compatible with block B, in the amount of 10 to 200 parts per hundred parts of the ABA block copolymer.

Triblock copolymers useful in the practice of 5 the present invention are described in U.S. 4,427,837 and EPO Publication 135,168.

ABA block copolymers suitable for use with the practice of the present invention require that the A block have an alpha-methylstyrene to styrene weight 0 ratio of from 2:98 to 98:2; and the preferred range is 1.1:1 to 2.5:1. The B block of the block copolymers is preferably polyisoprene, polybutadiene or isoprene- -butadiene copolymer. The ratio of the A block to the B block is from about 10:90 to 45:55 with a preferred 5 range of 15:85 and 30:70.

The triblock copolymers of the following examples and the method of their preparation are de¬ scribed in U.S. 4,427,837 and copending Patent Appli¬ cation Serial No. 630,906 filed July 13, 1984. In the 0 preparation of the triblock copolymers, conventional

anionic polymerization techniques were employed. Air and moisture were excluded from the reaction vessels and monomers were purified by passing them through alimina columns or by distilling them under nitrogen or 5 vaccuum in the presence of a drying agent. The di- functional organolithium initiator employed is described in U.S. Letters Patent 4,196,154 and U.S. 4,172,190.

The initiator was prepared in toluene solution by reacting secondary butyllithium with l,3-bis(l-phenyl- 10 ethenyl)benzene in a mole ratio of 2 to 1 at room temperature for a period of about 45 to 60 minutes. The concentration of the initiator solutions used in the experiments range from about 0.05 normal to 0.02 normal.

15. Many low molecular weight resins may be employed as tackifiers such as: rosin ester types as are commercially available under the trade designation of Floral 85; polyterpene such as is commercially available under the name Wingtac 95; polyolefin resins, 0 such as Super Sta-Tac 80; polydipentenes such as Zonarez 7085; polypinenes such as Zonarez 5. Stabilizers are generally of the hindered phenol type and are well known and common in the art.

The pressure sensitive adhesive compositions 5 of the present invention can contain up to 5 parts per hundred parts by weight of the ABA block copolymer of such materials as antioxidants and stabilizers. These include stabilizers for protection of both the diene center blocks and the non-elastomeric terminal blocks. 0 Combinations of stabilizers are often more effective, due to the different mechanisms of degradation to which

each of these types of blocks is subject. Certain hindered phenols, organo-metallic compounds, aromatic amines and sulfur compounds are useful for this purpose. Especially effective types of these materials include the following:

(1) Benzothiazoles, such as 2-(dialkyl-hydroxy- benzylthio)benzothiazoles,

(2) Esters of hydroxybenzyl alcohols, such as benzoates, phthalates, stearates, adi- pates or acrylates of 3,5-dialkyl-4-hydroxybenzyl alcohols,

(3) Stannous phenyl catecholates, (4) Zinc dialkyl dithiocarbamates,

(5) Alkyl phenols, e.g., 2,6-di-tert-butyl- -4-methyl phenol.

The tackifying resins employed together with the subject block copolymers and tackifying resin are represented by the following:

Rosin

Dehydrogenated rosin

Rosin + polyterpene resins, e.g., polymerized betapinene. (from 100% rosin to 100% resin) Glycerol esters of hydrogenated rosin

Pentaerythritol esters of hydrogenated rosin

Coumarone-indene resins

Hydrogenated rosin

Glycerol esters of polymerized rosin Maleic anhydride-modified rosin and rosin derivatives

Partial esters of styrene-maleic acid copolymers

Chlorinated biphenyls (S.P. 113-320°F.) Oil-soluble phenol-aldehyde resin

The diblock copolymers of the AB type which can optionally be included in the present pressure sensitive adhesive compositions are well known to those skilled in the art, as are processes for preparation of such diblock copolymers. These can be added in amounts up to 50 parts by weight per hundred parts of the ABA triblock copolymer. If desired, sometimes uninten- tionally, the optional diblock copolymer can be prepared in these amounts in the polymerization reaction that prepares the ABA triblock copolymer.

An extending oil can be used in the pressure sensitive adhesive in amounts up 50 parts by weight per hundred parts of the ABA block copolymer. The extender oils employed together with the tackifying resins and block copolymesrs have the chief advantage of substantially reducing the cost of the composition while improving tack and flexibility without any material degradation in other properties thereof. The oils must be chosen with care to coordinate with the block copolymer rela¬ tive to the compatability with the several polymer blocks present therein. The oil should be one which is substantially compatible with homopolymers of conjugated dienes but which is substantially incompatible with homopolymers of the nonelastic (thermoplastic) terminal blocks. Compatibility can be determined by the following type of test.

An oil to be tested is mixed in several pro¬ portions, e.g., 5, 25, 50 parts oil per hundred parts ABA polymer resin (phr. ) with the type of block copolymer

of interest in a volatile mutual solvent, for example, toluene. A thin film is cast by spreading the solution evenly on a glass surface and allowing the solvent, toluene, to evaporate over a period of 16-24 hours at ambient temperature. Suitability of the oil for use as an extender is judged by the tensile strengths of the oil-containing polymer films determined by an appropriate testing instrument and by the appearance of the film surface. Excessive compatibility with the terminal polymer segments will cause severe loss of tensile strength, greater than that resulting from simple dilution of the polymer. Excessive incompatiblity will be evidenced by diffusion of the oil to the film surface.

It is sometimes desirable to use a reinforcing resin in the present pressure sensitive adhesive composi¬ tions, which reinforcing resins have a higher softening point than the block A in the ABA polymer. Reinforcing resins suitable for the practice of the present invention are thermoplastic resins preferably having a glass transition temperature at least about 10° centigrade above the glass transition temperature of the A block of the ABA block copolymer. Typical of resins useful for reinforcement are poly(alphamethyl styrene), poly (2,6-dimethyl phenylene oxide) resins and a coumarone- -indene resin, an example of which is commercially available under the trade designation Cumar LX-509. Such resins are used in amounts up to 100 parts by weight per hundred parts of the ABA block copolymer, preferably from 2 to 100 parts.

The compositions of the present invention can be designed for a wide variety of uses and applications. They may be applied, for example, to paper, paper

boards, wood, metal foils, polyolefin films, polyvinyl chloride films, cellophane, felts, woven fabrics, non-woven fabrics and glass and for bonding two or more of such materials together. The adhesives are useful in pressure sensitive tapes such as masking tapes, adhesive sheets, primers for other adhesives, adhesive tapes, mending tapes, electrical insulation tape, laminates, hot-melt adhesives, mastics, cements, caulking compounds, binders, sealants, pressure sensitive adhesives otherwise, delayed tack adhesives, adhesive latices, shoe sole adhesives, cloth backings, carpet backings and cements.

Pressure sensitive adhesives of the present invention can be applied to substrates as a hot melt, for example, by extrusion from a sheeting die or slot die. Alternatively the compositions can be deposited from a solution such as 15 weight percent solution in 9:1 by volume toluene-methanol solvent. The invention is further illustrated but not limited by the following experiments.

The initiator solution used in the following experiments was prepared in toluene solution by reacting secondary butyl lithium with l,3-bis(l-phenzlethenyl) benzene in a mole ratio of 2 to 1 at room temperature for a period of about 45 to 60 minutes. The concen¬ tration of the initiator solutions used in the experi¬ ments range from about 0.05 normal to 0.02 normal.

Experiment 1.

A 2-liter reactor was charged with 1,225.8 grams of alpha-methylstyrene. A sec-butyllithium solution was slowly added to the alpha-methylstyrene

until a faint straw color appeared titrating the.impur¬ ities in the alphamethylstyrene. When the titration was complete, 177.4 grams of isoprene and 12 grams of styrene were added to the reactor. The reaction mix- ture was heated to 45 degrees centigrade whereupon 1.53 millimoles of the above-described difunctional initiator were added. The reaction mixture was heated to 50 degrees centigrade whereupon the heat of_ polymerization raised the temperature of the reactants to about 75 degrees centigrade in about 30 minutes. As the temper¬ ature of the reaction mixture started to return to 50 degrees, the color of the reaction mixture changed from a pale straw color to a brownish orange indicating that the polymerization of isoprene was complete and that the copolymerization of styrene and alpha-methylstyrene had begun. The temperature of the reaction mixture was maintained above 50 degrees centigrade for an additional 45 minute period and a mixture.of ispropenol and toluene, 10 to 1 by volume, was added slowly to the reaction mixture until the color began to fade. The reaction mixture was then heated to a temperature of 70 degrees for an addition period of 15 minutes and cooled to room temperature. About 130 grams of the reaction mixture was removed for analysis. To the remainder of the reaction mixture 154.7 grams of isoprene, 10.5 grams of styrene were added. The mixture was then heated to 45 degrees centigrade and 1.33 millimoles of the difunc- tional initiator solution was added. The second polymer¬ ization was permitted to proceed similarly for about 2 hours. The reaction mixture was terminated by the addition of 2 milliliters of isopropanol. A hindered phenol stabilizer in an amount of 3.7 grams was added and the excess alpha-methylstyrene monomer was removed by heating in a vacuum oven. The total yield was 333

grams. The polymer was an ABA triblock with polyiso- prene as the center block and alpha-methylstyrene- -styrene copolymer as the end blocks. The composition as determined by proton nuclear magnetic resonance was 81 weight percent isoprene, 12.7 weight percent alpha- -meth 1styrene and 6.3 weight percent styrene. The molecular weight of the polymer as determined by gel permeation chromatography was 176,000 molecular weight units.

The block copolymer was then mixed with an aliphatic hydrocarbon tackifying resin commercially designated as ESCOREZ 1310 commercially available from the Exxon Chemical Company. Varying proportions were employed as set forth in Table I ^" below. Included in the mixture was one part by weight per hundred parts by weight of resin of a solid hindered phenol stabilizer commercially available under the trade designation IRGANOX 1010 and available from Ciba-Geigy Corporation. Formulations were dissolved in toluene and applied to polyester film as toluene solutions; roughly equal parts of toluene and the adhesive formulation were used. Various physical properties were then determined. The peel strength shown in Table I is based on the Pressure Sensitive Tape Council (PSTC) test method PSTC-1. The rolling ball tack test was based on PSTC-6. The quick stick test employed was PSTC-5. The shear holding test was based on test method PSTC-7 and was conducted at 80.6°C (177 degrees Fahrenheit) with a 450 gram weight attached to the specimen; holding time in minutes is set forth in the Table.

TABLE I

ADHESIVE PERFORMANCE OF COMPOSITIONS CONTAINING TRIBLOCK PREPARED IN EXAMPLE 1.

ABA polymer Wt.% 73.5 69.9 66.7 62.5 61.0 58.8 55.0 . 50.0 Escorez 1310 Wt.% 26.5 30.1 33.3 37,5 39.0 41.2 45.0 50.0

Rolling ball tack 4.0 5.0 4.5 4.5 5.0 4.5 12.0 >26 in cm

180° Peel strength 44.4 41.1 48.9 46.4 46.4 53.9 66.0 75. .5 in kg/m(in lb/in) (2.49) (2.3) (2.74) (2.6) (2.6) (3.02) (3.7) (4, .23)

Quick stick in 33,2 23.9 34.6 30.9 22.7 26.1 39.3 48. .9 kg/m(in lb/in) (1.86) (1.34) (1.94) (1.73) (1.27) (1.46) (2.2) (2. .74)

Holding time all >4100 in min

Wt. % = Weight percent cm = centimeter kg/m = kilograms per meter lb/in = pounds per inch min = minute

For purposes of comparison similar formulations were prepared utilizing a commercially available styrene isoprene triblock copolymer available under the trade designation Kraton 1107. The commercially available block copolymer contained 86 percent by weight isoprene and 14 weight percent styrene polymerized therein. Molecular weight as determined by gel permeation chromatography was 169,000 molecular weight units. The results are set forth in Table II.

TABLE II

ADHESIVE PERFORMANCE OF COMPOSITIONS CONTAINING A COMMERCIAL STYRENE-ISOPRENE TRIBLOCK POLYMER COMPARATIVE EXPERIMENTS-NOT EXAMPLES OF THE PRESENT INVENTION

ABA polymer Wt.% 75 70 65 62 60 55 50 45 Escorez 1310 Wt.% 25 30 35 38 40 45 50 55

Rolling ball tack 3.0 2.0 3.5 4.0 5.0 4.5 14.0 26.0 in cm

180° Peel strength 43.4 48.2 50.0 55.3 53.6 71.4 85.7 91.0 in kg/m (in lb/in) (2.43) (2.7) (2.8) (3.1) (3.0) (4.0) (4.8) (5.1

Quick stick in kg/m 20.5 24.3 26.2 32.5 31.8 36.1 38.0 40.3 (in lb/in) (1-15) (1.36) (1.47) (1.82) (1.78) (2.02) (2.13) (2.2

Holding time . 2978 2436 1633 1085 984 961 730 310 in min

Wt.% = Weight percent cm = centimeter kg/m = kilograms per meter lb/in - pounds per inch min = minute

The 55/45 compositions of both Tables I and II were used to prepare each a 50 weight percent solution in toluene. A brookfield viscometer rotating at 5 rpm at room temperature indicated the solution viscosity of the composition in accordance with the present invention to be 4.3 pascal seconds. The comparative example composition containing the commercial triblock polymer had a viscosity of 6.6 pascal seconds. The lower solution viscosity provides a material that is easier to apply. However, the holding time at higher temper¬ ature is considerably greater with compositions in accordance with the invention as exemplified by the tables.

A further series of pressure sensitive adhesive compositions were prepared from the ABA copolymer prepared in Experiment 1 and evaluated in the herein¬ before discussed manner. The test results are set forth in Table III. The tackifying resin used was an aliphatic hydrocarbon resin commercially available under the tradename Piccolyte A115 from Hercules.

CONTAINING TRIBLOCK PREPARED IN EXAMPLE 1

ABA polymer Wt.% 73.5 69.9 66.7 62.5 61.0 ' 58.5 55.0 Piccolyte A115 Wt.% 26.5 30.1 33.3 37.5 39.0 41 ^* .2 45.0

Rolling ball tack 3.0 4.β 4.0 5.0 7.0 8.0 17.0 in cm

180° Peel strength 53.6 58.0 56.6 79.8 80.3 82.5 107.1 in kg/m (in lb/in) (3.0) (3.25 (3.17) (4.47) (4.5) (4.62) (6.0)

-J>

Quick stick in kg/m 42.8 44.6 42.1 51.8 53 i6 51.8 55.3 I (in lb/in) (2.4) (2.5) (2.36) (2.9) (3.0) (2.9) (3.1)

Holding time all >4100 in min

Wt.% = Weight percent cm = centimeter kg/m = kilograms per meter lb/in = pounds per inch min = minute

Experi ent 2.

Another triblock copolymer composition was prepared by the method described in Experiment 1 with the exception that a slightly larger amount of initiator was used in each of the two polymerization steps. The resultant block copolymer had an identical composition as to the block copolymer prepared in Experiment 1; howeve the molecular weight as measured by gel permeation chromatography was 155,000 molecular weight units.

Two series of experiments were conducted; one using Escorez 1310 as the tackifier and the other using Piccolyte A115 as the tackifier. The results are set forth in Tables IV and V.

T BLέ IV

ADHESIVE PERFORMANCE OF COMPOSITIONS CONTAINING TRIBLOCK PREPARED IN EXAMPLE

ABA polymer Wt. % 65 60 55 50 45 40 Escorez 1310 Wt.% 35 40 45 50 55 60

Rolling ball tack 3.0 2.0 3.0 6.0 8.0 no tack in cm

180° Peel Strength 59.4 69.1 82.6 93.5 109.2 ON in kg/m (in lb/in) (3.33) (3.87) (4.63) (5.24) (6.12) I

Quick stick in kg/m 32.7 36.4 37 5 39.3 43.4 (in lb/in) (1.83) (2.04) (2 10) (2.20) (2.43)

Holding time all >4100 in min

Wt. % = weight percent cm = centimeter kg/m = kilograms per meter lb/in = pound per inch min = minute

TABLE V

ADHESIVE PERFORMANCE OF COMPOSITIONS CONTAINING TRIBLOCK

ABA polymer Wt. % 65 60 55 50 45 40 Piccolyte A115 Wt.% 35 40 45 50 55 60

Rolling ball tack 12.0 12.0 13.0 >26 no tack no tack in cm

180° Peel strength 73 .1 73 .0 80 .0 94.8 in kg/m (in lb/in) (4.1 ) (4.09 ) (4.48 ) ( 5.31 )

I

Quick stick in kg/m 35.9 36.1 38.9 40.2 (in lb/in) (2.01) (2.02) (2.18) (2.25)

Holding time all >4100 in min

Wt. % = Weight percent cm = centimeter kg/m = kilograms per meter lb/in = pounds per inch min = minute

Two compositions were prepared. One, Compos¬ ition A contained 50 weight percent of the block copolymer prepared in Experiment 2 and 50 weight percent Escorez 1310. The second, Composition B was 55 weight percent Kraton 1107 and 45 weight percent Escorez 1310 and was a comparative example, not an example of the present invention. These compositions were selected for compar¬ ison because from the data in Table II and Table V they showed comparable tack, peel strength and quick stick. The Brookfield viscosities were determined at various temperatures and are set forth in Table VI in pascal seconds (Pa.s).

TABLE VI

BROOKFIELD VISCOSITIES OF ADHESIVE COMPOSITIONS IN Pa.s

Temperature in °C 168 179 191 204 Degrees Fahrenheit(°F) (335) (355) (375) ^' (400)

Composition A 26.1 17.0 12.0 7.0

Composition B* 26.1 24.5 15.5 10.7 *Comparative example, not an example of the present invention

The data in Table VI clearly discloses that compositions in accordance with the present invention have lower viscosities at higher temperatures than the conven¬ tionally used resins.

Experiment 3♦

A 0.11 cubic meter (30 gallon) nitrogen filled reactor was charged with 61.1 kilograms of alpha-methylstyrene, 6.55 kilograms of butadiene and 1.46 kilograms of styrene. An aliquot amount of the charge was withdrawn from the reactor. To this aliquot a small amount of tetrahydrofuran was added and a sec-butyllithium solution in cyclohexane was added

until color appeared. Based on the titration the amount of impurities in the remaining feed which was 59.42 kilograms of alpha-methylstyrene, 6.37 kilograms of butadiene, and 1.42 kilograms of styrene was deter- mined to be equivalent to 41.6 milliequivalents of sec- butyllithium. The content of the reactor was heated to 40 degrees centigrade and 163.8 millimoles of the above-described difunctional lithium initiator was added. Polymerization started shortly after the initi- ator addition and was completed in about two and one-half hours during which time the temperature of the reactor rose to a maximum of 87 degrees centigrade. The resul¬ tant product was a triblock copolymer having the ABA configuration in which block A was an alpha-methyl- styrene and styrene copo.lymer and the B block was a polybutadiene. The product was soluble in the alpha- methylstyrene monomer used as solvent in the polymer¬ ization. A solution of 13.4 milliliters of isopropanol in 20 milliliters of toluene was added to terminate a majority of ^' the active chain ends. The resultant solution was then maintained at 75 degrees centigrade for 30 minutes to insure all reactive chain ends were terminated. After the reaction mixtue had cooled to room temperature, a small sample was withdrawn for analysis. To the remaining solution 1.384 kilograms of styrene and 6.94 kilograms of butadiene was added. The solution was heated to 46 degrees centigrade and a second addition of 152 millimoles of the difunctional initiator was added. The second polymerization lasted for about one and one-half hours and the product was similar to that of the first polymerization. The reaction was terminated by the addition of 51.2 mil- lilters of isopropanol. A hindered phenol stabilizer commercially available under the trade designation of

Isonox 129 from Schenectady Chemicals was added in a quantity bf 42.2 grams and the reactor left undisturbed overnight. Additional stabilizers were added the following day before the product was recovered from the excess alpha-methylstyrene by drying in a heated vacuum oven. Final yield was 19.5 kilograms of ABA block copolymer containing 64.1 weight percent butadiene,

13.3 weight percent styrene and 22.6 weight percent alphamethy1styrene. The molecular weight was deter- mined to be 78,000 molecular weight units by gel permea¬ tion chromatography. The resultant ABA block copolymer was mixed with a hydrogenated hydrocarbon resin tackifier commercially available under the trade designation of Escorez 5380 from Exxon Chemical Company and a stabilizer commercially available under the trade designation of IRGANOX 1010. The materials were combined in a weight ratio of 60, 40 and 1 respectively.

For purposes of evaluation samples were pre¬ pared by the solution method as delineated in Experiment 1. The rolling ball tack value was 15 centimeters; the peel strength was 32.1 kilograms per meter (1.8 pounds per inch) and the quick stick as tested by test method PSTC-5 was 25.0 kilograms per meter (1.4 pounds per inch).

A second combination was prepared containing

50 parts by weight of the block copolymer prepared above and 40 parts by weight of Zonatac 105 and 10 parts by weight Zonarez A25. Evaluation indicating its tack was 16 centimeters, peel strength was 39.3 kilograms per meter (2.2 pounds per inch) and quick stick was

21.4 kilograms per meter (1.2 pounds per inch). Zonatac and Zonarez A25 are polyterpene tackifiers obtained from Arizona Chemical Company.

Experi ent 4.

A one-liter glass reactor was nitrogen purged and charged with 400 milliliters of alpha-methylstyrene. A small amount of sec-butyllithium solution was added slowly until a faint straw color appeared. The reactor was then charged with 49 grams of isoprene and 3.8 grams of styrene. The reaction mixture was heated to 45 degrees centigrade and 0.45 millimole of the above- -described difunctional initiator solution was added. The reaction mixture was heated to 50 degrees centigrade and maintained at or above 50 degrees centigrade for about two hours. During the two-hour period, the temperature had risen to a maximum of 95 degrees centigrade and the color had changed to a brownish orange. To terminate the reaction, 0.5 milliliter of acetic acid was added. The polymer was recovered from the excess alpha-methylstyrene by precipitating with methanol from the reaction mixture and again from a methylene chloride solution. The resultant polymer was an ABA triblock with polyisoprene as the center block and alpha-methyl¬ styrene styrene copolymer as the end blocks. About 50 grams of product was obtained, having a composition of 81.2 weight percent isoprene, 12.5 weight percent alpha-methylstyrene and 6.3 weight percent styrene. The molecular weight as determined by gel permeation chromatography was 212,000.

A solution of 60 parts of the triblock copolymer with 40 parts by weight of Escorez 1310 was dissolved in toluene and applied to polyester film for further evaluation. The peel strength was determined to be 50 kilograms per meter (2.8 pounds per inch), the rolling ball tack was 15 centimeters and quick stick was 28.6 kilograms per meter (1.6 pounds per inch).

Experiment 5.

The polymerization procedure of Experiment 4 was repeated with the exception that 1 millimeter of isoprene was added to the difunctional initiator solution and the initiator solution was then heated to 70 degrees centigrade for a period of 7 minutes before use. The reactor was fed only alpha-methylstyrene and isoprene. The required amount of styrene was added when the temperature of the reaction mixture rose to its maximum. The resulting triblock copolymer had the same composition as the copolymer of Experiment 4 except that the structure was less tapered. The molecular weight as determined by gel permeation chromatography was 196,000 molecular weight units. 60 parts of the resultant ABA copolymer were mixed with 40 parts by weight of Escorez 1310 dissolved in toluene and applied to a polyester film for evaluation. The peel strength was determined to be 62.5 kilograms per meter (3.5 pounds per inch); the rolling ball tack was 9 centimeters; and the quick stick value was 37.5 kilograms per meter (2.1 pounds per inch) .

Experiment 6.

The polymerization procedure of Experiment 4 was repeated with the following exceptions: 10.9 grams of butadiene was used, and 31.3 grams of isoprene. The initiator was .73 millimoles of the hereinbefore described difunctional initiator. The quantity of styrene used was 4.5 grams and was withheld from the feed until the polymerization temperature of the diene monomer reached its maximum value. The polymer recovered was an ABA . triblock polymer with an isoprene/butadiene copolymer as the center block and an alpha-methylstyrene/styrene copolymer as the end blocks. The composition was 19.7

percent by weight butadiene, 56.6 percent by weight isoprene, 15.5 percent by weight alpha-methylstryene and 8.2 percent by weight styrene. The molecular weight as determined by gel permeation chromatography was 123,000 molecular weight units.

Its value in a pressure sensitive adhesive formulation was determined by admixing 60 parts of the block copolymer with 40 parts of Escorez 1310 in toluene and applying to polyester film, as in Experiment 1. The peel strength was 58.9 kilograms per meter (3.3 pounds per inch); the rolling ball tack just exceeded 26 centimeters and the quick stick value was 42.8 kilograms per meter (2.4 pounds per inch).