Styrene-butadiene rubber copolymer anionic polymerization

Butadiene copolymers are mainly prepared to yield mbbers (see Styrene-butadiene rubber). Many commercially significant latex paints are based on styrene—butadiene copolymers (see Coatings Paint). In latex paint the weight ratio S B is usually 60 40 with high conversion. Most of the block copolymers prepared by anionic catalysts, eg, butyUithium, are also elastomers. However, some of these block copolymers are thermoplastic mbbers, which behave like cross-linked mbbers at room temperature but show regular thermoplastic flow at elevated temperatures (45,46). Diblock (styrene—butadiene (SB)) and triblock (styrene—butadiene—styrene (SBS)) copolymers are commercially available. Typically, they are blended with PS to achieve a desirable property, eg, improved clarity/flexibiHty (see Polymerblends) (46). These block copolymers represent a class of new and interesting polymeric materials (47,48). Of particular interest are their morphologies (49—52), solution properties (53,54), and mechanical behavior (55,56). 

The most important hydrocarbon copolymers are styrene-butadiene rubbers (SBR) produced by free-radical emulsion or anionic polymerization. Anionic polymerization allows the manufacture of styrene-butadiene and styrene-isoprene three-block copolymers. 

Styrene-butadiene rubber (SBR) for automobile tires is a random copolymer. It is prepared by two methods, free-radical and anionic polymerization, both of which are carried out on a mixture of styrene and 1,3-butadiene. Free-radical initiation is essentially nonselective and gives the random copolymer. Anionic initiation is carried out under conditions designed to equalize the reactivity of the two monomers so as to ensure randomness. 

A common material made by anionic polymerization is the random copolymer composed of a roughly 1 3 mixture of polystyrene and polybutadiene known as SBR (for styrene butadiene rubber). Both of these monomers are compatible with anionic polymerization, and indeed SBR is made this way as a popular substitute for natural rubber, often used in the automotive industry. Styrene and butadiene are also both compatible with radical polymerization, and SBR can be made under emulsion polymerization conditions using radical initiators. 

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. 

Over 5.5 billion pounds of synthetic rubber is produced annually in the United States. The principle elastomer is the copolymer of butadiene (75%) and styrene (25) (SBR) produced at an annual rate of over 1 million tons by the emulsion polymerization of butadiene and styrene. The copolymer of butadiene and acrylonitrile (Buna-H, NBR) is also produced by the emulsion process at an annual rate of about 200 million pounds. Likewise, neoprene is produced by the emulsion polymerization of chloroprene at an annual rate of over 125,000 t. Butyl rubber is produced by the low-temperature cationic copolymerization of isobutylene (90%) and isoprene (10%) at an annual rate of about 150,000 t. Polybutadiene, polyisoprene, and EPDM are produced by the anionic polymerization of about 600,000, 100,000, and 350,000 t, respectively. Many other elastomers are also produced. 

Most polystyrene products are not homopolystyrene since the latter is relatively brittle with low impact and solvent resistance (Secs. 3-14b, 6-la). Various combinations of copolymerization and blending are used to improve the properties of polystyrene [Moore, 1989]. Copolymerization of styrene with 1,3-butadiene imparts sufficient flexibility to yield elastomeric products [styrene-1,3-butadiene rubbers (SBR)]. Most SBR rubbers (trade names Buna, GR-S, Philprene) are about 25% styrene-75% 1,3-butadiene copolymer produced by emulsion polymerization some are produced by anionic polymerization. About 2 billion pounds per year are produced in the United States. SBR is similar to natural rubber in tensile strength, has somewhat better ozone resistance and weatherability but has poorer resilience and greater heat buildup. SBR can be blended with oil (referred to as oil-extended SBR) to lower raw material costs without excessive loss of physical properties. SBR is also blended with other polymers to combine properties. The major use for SBR is in tires. Other uses include belting, hose, molded and extruded goods, flooring, shoe soles, coated fabrics, and electrical insulation. 

The development of high styrene content styrene-butadiene copolymers (SBCs), such as K-Resin SBC, is best thought of as a branch off the history of anionic polymerization and rubber. A number of excellent reviews cover this aspect of the subject in great detail, and should be obtained for detailed examination of the history of rubber and anionically synthesized rubber polymers [1-3]. What follows is a brief overview to fit the high styrene content SBC into a historical context. 

The most extensively studied block copolymers prepared by anionic polymerization are the styrene-butadiene or styrene-isoprene rubbers. Shell Chemical Company s Kraton thermoplastic elastomers are ABA block copolymers of this type. Their elastomeric properties are excellent, yet they differ from other rubbers in that vulcanization is not required. These elastomers consist of a rubbery polybutadiene matrix with the styrene segments serving as anchors in thermoplastic microdomains. 

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