Butadiene-styrene-isoprene

Synthetic rubber), for example, acrylate, acrylate-butadiene, butyl, ethylene-propylene, chloroprene, ethylene-propylene diene, latex, neoprene, nitrile-butadiene, polyisobutylene, polysulfide, silicone, styrene-butadiene, styrene-isoprene rubber thermoset vulcanizable elastomers thiol rubber urethane... 

Styrene-Butadiene-Styrene Block Copolymers. Styrene blocks associate into domains that form hard regions. The midblock, which is normally butadiene, ethylene-butene, or isoprene blocks, forms the soft domains. Polystyrene domains serve as cross-links. 

G-5—G-9 Aromatic Modified Aliphatic Petroleum Resins. Compatibihty with base polymers is an essential aspect of hydrocarbon resins in whatever appHcation they are used. As an example, piperylene—2-methyl-2-butene based resins are substantially inadequate in enhancing the tack of 1,3-butadiene—styrene based random and block copolymers in pressure sensitive adhesive appHcations. The copolymerization of a-methylstyrene with piperylenes effectively enhances the tack properties of styrene—butadiene copolymers and styrene—isoprene copolymers in adhesive appHcations (40,41). Introduction of aromaticity into hydrocarbon resins serves to increase the solubiHty parameter of resins, resulting in improved compatibiHty with base polymers. However, the nature of the aromatic monomer also serves as a handle for molecular weight and softening point control. 

Natural mbber comes generally from southeast Asia. Synthetic mbbers are produced from monomers obtained from the cracking and refining of petroleum (qv). The most common monomers are styrene, butadiene, isobutylene, isoprene, ethylene, propylene, and acrylonitrile. There are numerous others for specialty elastomers which include acryUcs, chlorosulfonated polyethylene, chlorinated polyethylene, epichlorohydrin, ethylene—acryUc, ethylene octene mbber, ethylene—propylene mbber, fluoroelastomers, polynorbomene, polysulftdes, siUcone, thermoplastic elastomers, urethanes, and ethylene—vinyl acetate. 

Ring Additions Catalyzed by Alkali Metals. The addition of tributyltin chloride and olefins such as styrene, isoprene, or butadiene to sulfolane is cataly2ed by alkah metals, including sodium and lithium, and by sodium amide (10—13). The addition of tributyltin chloride to sulfolane in the... 

Commercially, anionic polymerization is limited to three monomers styrene, butadiene, and isoprene [78-79-5], therefore only two useful A—B—A block copolymers, S—B—S and S—I—S, can be produced direcdy. In both cases, the elastomer segments contain double bonds which are reactive and limit the stabhity of the product. To improve stabhity, the polybutadiene mid-segment can be polymerized as a random mixture of two stmctural forms, the 1,4 and 1,2 isomers, by addition of an inert polar material to the polymerization solvent ethers and amines have been suggested for this purpose (46). Upon hydrogenation, these isomers give a copolymer of ethylene and butylene. 

Styrene isoprene block copolymers Styrene butadiene block copolymers Styrene butadiene random copolymers Polyisobutylene Polysiloxanes... 

Block copolymer chemistry and architecture is well described in polymer textbooks and monographs [40]. The block copolymers of PSA interest consist of anionically polymerized styrene-isoprene or styrene-butadiene diblocks usually terminating with a second styrene block to form an SIS or SBS triblock, or terminating at a central nucleus to form a radial or star polymer (SI) . Representative structures are shown in Fig. 5. For most PSA formulations the softer SIS is preferred over SBS. In many respects, SIS may be treated as a thermoplastic, thermoprocessible natural rubber with a somewhat higher modulus due to filler effect of the polystyrene fraction. Two longer reviews [41,42] of styrenic block copolymer PSAs have been published. 

Currently, important TPE s include blends of semicrystalline thermoplastic polyolefins such as propylene copolymers, with ethylene-propylene terepolymer elastomer. Block copolymers of styrene with other monomers such as butadiene, isoprene, and ethylene or ethylene/propy-lene are the most widely used TPE s. Styrene-butadiene-styrene (SBS) accounted for 70% of global styrene block copolymers (SBC). Currently, global capacity of SBC is approximately 1.1 million tons. Polyurethane thermoplastic elastomers are relatively more expensive then other TPE s. However, they are noted for their flexibility, strength, toughness, and abrasion and chemical resistance. Blends of polyvinyl chloride with elastomers such as butyl are widely used in Japan. ... 

Table IV shows the data on rigidity changes of the end-sealing compounds at two dose levels. Rigidity was determined by torsional braid analysis (5). These data indicate that the blend of cured and uncured isobutylene-isoprene copolymer was softened most by the irradiation treatment, the blend of polychloroprene and butadiene-styrene copolymer softened the least, and the blend of polychloroprene and the uncured isobutylene-isoprene copolymer was intermediate. Increasing the irradiation dose from 3-4 Mrad to 6-7.5 Mrad decreased the rigidity of the three end-sealing compounds. The irradiation temperature did not significantly influence rigidity.

Experimentally, the stretching of block copolymer chains has been addressed in two ways by measuring L as a function of N, and by measuring the components of Rg of the block chains both parallel and perpendicular to the interface. The domain dimensions have been studied most extensively for styrene-isoprene and styrene-butadiene block copolymers X-ray and neutron scattering are the methods of choice. The predicted SSL scaling of L N2/3 has been reported for spheres, cylinders and lamellae [99,102-106], but not in all cases. For example, Bates et al. found N0 37 for styrene-butadiene spheres [100], and Hadziioannou and Skoulios observed N0 79 for styrene-isoprene lamellae [107], In the sphere case, kinetic limitations to equilibration were felt to be an important factor [100],... 

Emulsion polymerization is the most important process for production of elastic polymers based on butadiene. Copolymers of butadiene with styrene and acrylonitrile have attained particular significance. Polymerized 2-chlorobutadiene is known as chloroprene rubber. Emulsion polymerization provides the advantage of running a low viscosity during the entire time of polymerization. Hence the temperature can easily be controlled. The polymerizate is formed as a latex similar to natural rubber latex. In this way the production of mixed lattices is relieved. The temperature of polymerization is usually 50°C. Low-temperature polymerization is carried out by the help of redox systems at a temperature of 5°C. This kind of polymerization leads to a higher amount of desired trans-1,4 structures instead of cis-1,4 structures. Chloroprene rubber from poly-2-chlorbutadiene is equally formed by emulsion polymerization. Chloroprene polymerizes considerably more rapidly than butadiene and isoprene. Especially in low-temperature polymerization emulsifiers must show good solubility and... 

Linear triblock copolymers of the type styrene-butadiene-styrene (SBS) and styrene-isoprene-styrene (SIS) are produced commercially by anionic polymerization through sequential addition of monomers in the reaction chamber [10] as shown below ... 

The isoprene units in the copolymer impart the ability to crosslink the product. Polystyrene is far too rigid to be used as an elastomer but styrene copolymers with 1,3-butadiene (SBR rubber) are quite flexible and rubbery. Polyethylene is a crystalline plastic while ethylene-propylene copolymers and terpolymers of ethylene, propylene and diene (e.g., dicyclopentadiene, hexa-1,4-diene, 2-ethylidenenorborn-5-ene) are elastomers (EPR and EPDM rubbers). Nitrile or NBR rubber is a copolymer of acrylonitrile and 1,3-butadiene. Vinylidene fluoride-chlorotrifluoroethylene and olefin-acrylic ester copolymers and 1,3-butadiene-styrene-vinyl pyridine terpolymer are examples of specialty elastomers. 

Butadiene and isoprene have two double bonds, and they polymerize to polymers with one double bond per monomeric unit. Hence, these polymers have a high degree of unsaturation. Natural rubber is a linear cis-polyisoprene from 1,4-addition. The corresponding trans structure is that of gutta-percha. Synthetic polybutadienes and polyisoprenes and their copolymers usually contain numerous short-chain side branches, resulting from 1,2-additions during the polymerization. Polymers and copolymers of butadiene and isoprene as well as copolymers of butadiene with styrene (GR-S or Buna-S) and copolymers of butadiene with acrylonitrile (GR-N, Buna-N or Perbunan) have been found to cross-link under irradiation. 

Diene polymers refer to polymers synthesized from monomers that contain two carbon-carbon double bonds (i.e., diene monomers). Butadiene and isoprene are typical diene monomers (see Scheme 19.1). Butadiene monomers can link to each other in three ways to produce ds-1,4-polybutadiene, trans-l,4-polybutadi-ene and 1,2-polybutadiene, while isoprene monomers can link to each other in four ways. These dienes are the fundamental monomers which are used to synthesize most synthetic rubbers. Typical diene polymers include polyisoprene, polybutadiene and polychloroprene. Diene-based polymers usually refer to diene polymers as well as to those copolymers of which at least one monomer is a diene. They include various copolymers of diene monomers with other monomers, such as poly(butadiene-styrene) and nitrile butadiene rubbers. Except for natural polyisoprene, which is derived from the sap of the rubber tree, Hevea brasiliensis, all other diene-based polymers are prepared synthetically by polymerization methods. 

Titanocene (Cp2TiR2) /alkyllithium (LiR) Styrene, butadiene or isoprene copolymers PB in cyclohexane and toluene (5 wt.%) Catalyst (bis(cyclopentadienyl) titanium dichloride) 0.4 mmol per 100 g PB PH2 0.49 MPa T 40 °C t 2 h Conversion 97% Asahi Kasei Kogyo Kabushiki Kaisha (Osaka, Japan) 62 (1985)... 

Now again, a state of inhomogeneity in polymers, so especially interesting in films and interfaces, occur when discontinuities are built into the main valence chains and networks. Block polymers are the classic embodiments of this. Many periodic distances separating domains in such alternating or rhymthic copolymers have been reported. These indicate existence of phases in laminar domains and, in other cases, of spherical domains.(51) Cases are shown experimentally for styrene/isoprene copolymers and also for styrene/butadiene.(52,53,54)... 

The fairly broad most probable distribution for the rays may be considered as an undesirable imperfection of regular stars. Corresponding measurements with much narrower arm length distributions were made later, mainly by the research groups of Fetters [20, 30, 31] and Roovers [25, 26] which were obtained by living anionic polymerization of styrene, isoprene and butadiene respective-... 

Several studies have been published which utilize size exclusion chromatography (SEC) for characterization of the molecular weight distribution of multi-arm structures of polystyrene, polyisoprene, and block copolymers of styrene/ butadiene and styrene/isoprene (1, 2, 8, 17, 25-26). An... 

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