Polybutadienes properties

Acrylonitrile—Butadiene—Styrene. ABS is an important commercial polymer, with numerous apphcations. In the late 1950s, ABS was produced by emulsion grafting of styrene-acrylonitrile copolymers onto polybutadiene latex particles. This method continues to be the basis for a considerable volume of ABS manufacture. More recently, ABS has also been produced by continuous mass and mass-suspension processes (237). The various products may be mechanically blended for optimizing properties and cost. Brittle SAN, toughened by SAN-grafted ethylene—propylene and acrylate mbbets, is used in outdoor apphcations. Flame retardancy of ABS is improved by chlorinated PE and other flame-retarding additives (237). 

Carbon Cha.in Backbone Polymers. These polymers may be represented by (4) and considered derivatives of polyethylene, where n is the degree of polymeriza tion and R is (an alkyl group or) a functional group hydrogen (polyethylene), methyl (polypropylene), carboxyl (poly(acryhc acid)), chlorine (poly(vinyl chloride)), phenyl (polystyrene) hydroxyl (poly(vinyl alcohol)), ester (poly(vinyl acetate)), nitrile (polyacrylonitrile), vinyl (polybutadiene), etc. The functional groups and the molecular weight of the polymers, control thek properties which vary in hydrophobicity, solubiUty characteristics, glass-transition temperature, and crystallinity. 

Triisopropan olamine is used in natural mbber cross-linking and as a color stabilizer for polyethylene formulations. Chain termination of polybutadiene with triisopropan olamine gives improved cold-flow properties. 

The property of polybutadiene of most interest to the mbber compounder is excellent abrasion resistance coupled with excellent resilience. The polymer has very high rebound and low heat generation. With a few exceptions, such as the core of soHd golf balls, the polymer is blended with other polymers to take advantage of its excellent abrasion and rebound. Uses in North America are as follows tires, 500,000 t (74%) plastic modification,... 

Among the techniques employed to estimate the average molecular weight distribution of polymers are end-group analysis, dilute solution viscosity, reduction in vapor pressure, ebuUiometry, cryoscopy, vapor pressure osmometry, fractionation, hplc, phase distribution chromatography, field flow fractionation, and gel-permeation chromatography (gpc). For routine analysis of SBR polymers, gpc is widely accepted. Table 1 lists a number of physical properties of SBR (random) compared to natural mbber, solution polybutadiene, and SB block copolymer. 

Very high 4-addition (>80%) imparts more desirable properties for appHcations like heavy-duty tires (200). Stmctural properties of some typical polybutadienes are Hsted in Table 3 (200—202). 

Processings and Properties. Polybutadiene is compounded similarly to SBR and vulcanised with sulfur. The high cis-1,4 type crystallizes poorly on stretching so it is not suitable as a "gum" stock but requires carbon black reinforcement. It is generally used for automotive tires in mixtures with SBR and natural mbber. Its low T (—OS " C) makes it an excellent choice for low temperature tire traction, and also leads to a high resilience (better than natural mbber) which ia turn results ia a lower heat build-up. Furthermore, the high i j -polybutadiene also has a high abrasion resistance, a plus for better tire tread wear. 

This combination of monomers is unique in that the two are very different chemically, and in thek character in a polymer. Polybutadiene homopolymer has a low glass-transition temperature, remaining mbbery as low as —85° C, and is a very nonpolar substance with Htde resistance to hydrocarbon fluids such as oil or gasoline. Polyacrylonitrile, on the other hand, has a glass temperature of about 110°C, and is very polar and resistant to hydrocarbon fluids (see Acrylonitrile polymers). As a result, copolymerization of the two monomers at different ratios provides a wide choice of combinations of properties. In addition to providing the mbbery nature to the copolymer, butadiene also provides residual unsaturation, both in the main chain in the case of 1,4, or in a side chain in the case of 1,2 polymerization. This residual unsaturation is useful as a cure site for vulcanization by sulfur or by peroxides, but is also a weak point for chemical attack, such as oxidation, especially at elevated temperatures. As a result, all commercial NBR products contain small amounts ( 0.5-2.5%) of antioxidant to protect the polymer during its manufacture, storage, and use. 

Between the 1920s when the initial commercial development of mbbery elastomers based on 1,3-dienes began (5—7), and 1955 when transition metal catalysts were fkst used to prepare synthetic polyisoprene, researchers in the U.S. and Europe developed emulsion polybutadiene and styrene—butadiene copolymers as substitutes for natural mbber. However, the tire properties of these polymers were inferior to natural mbber compounds. In seeking to improve the synthetic material properties, research was conducted in many laboratories worldwide, especially in the U.S. under the Rubber Reserve Program. 

The Ekestone group also polymerized 1,3-butadiene to give an extremely high mol wt polybutadiene of 70% cis-1 4 stmcture. In thek research, they purposefully avoided the preparation of vinyl stmctures in both polyisoprene and polybutadiene since it was beheved that vinyl groups adversely affected tke performance. Since natural mbber was 99.9% cis-1 4 stmcture and had superior properties, they beheved that a 1,4 stmcture was necessary for acceptable physical properties. The addition of polar compounds to the hthium-catalyzed polymerization of butadiene changes the microstmcture from the 90% tij -l,4 stmcture to a mixed cis-1 4 and trans-1 4 microstmcture. 

Syndiotactic Polybutadiene. Syndiotactic polybutadiene is a unique material that combines the properties of plastic and mbber. It melts at high (150—220°C) temperatures, depending on the degree of crystallinity in the sample, and it can be molded into thin films that are flexible and have high elongation. The unique feature of this plastic-like material is that it can be blended with natural mbber. 1,4-Polybutadiene and the resulting blends exhibit a compatible formulation that combines the properties of plastic and mbber. 

Syndiotactic polybutadiene was fkst made by Natta in 1955 (28) with a melting point of 154°C. Syndiotactic polybutadiene [31567-90-5] can be prepared with various melting points depending on its vinyl content and degree of crystallinity. The physical, mechanical, and rheological properties of the polymer are gready affected by these parameters. 

The physical properties of low melting point (60—105°C) syndiotactic polybutadienes commercially available from JSR are shown in Table 1. The modulus, tensile strength, hardness, and impact strength all increase with melting point. These properties are typical of the polymer made with a cobalt catalyst modified with triphenylphosphine ligand. 

Table 1. Physical Properties of Low Melting Syndiotactic 1,2-Polybutadiene...

Fig. 5. Effect of 1,2-polybutadiene level on tine physical properties.

Based on this variety of properties, amorphous polybutadiene has found a niche in the mbber industry. Moreover, it appears that the anionicaHy prepared polymer is the only polymer that can be functionalized by polar groups. The functionalization is done by using aromatic substituted aldehydes and ketones or esters. Functionalization has been reported to dramatically improve polymer-filler interaction and reduce tread hysteresis (70—73). 

A large volume usage of S—B—S-based compounds is ia footwear. Canvas footwear, such as sneakers and unit soles, can be made by injection mol ding. Frictional properties resemble those of conventionally vulcanised mbbers and are superior to those of the flexible thermoplastics, such as plasticized poly(vinyl chloride). The products remain flexible under cold conditions because of the good low temperature properties of the polybutadiene segment. 

Rubber and Elastomers Rubber and elastomers are widely used as lining materials. To meet the demands of the chemical indus-tiy, rubber processors are continually improving their products. A number of synthetic rubbers have been developed, and while none has all the properties of natural rubber, they are superior in one or more ways. The isoprene and polybutadiene synthetic rubbers are duphcates of natural. 

Property polyisoprene) (GR-S) (polyisoprene) (nitrile) (neoprene) isoprene) Polybutadiene Polysulfide (polysiloxane)... 

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