Styrene-butadiene rubber differences

The elastomer produced in greatest amount is styrene-butadiene rubber (SBR) Annually just under 10 lb of SBR IS produced in the United States and al most all of it IS used in automobile tires As its name suggests SBR is prepared from styrene and 1 3 buta diene It is an example of a copolymer a polymer as sembled from two or more different monomers Free radical polymerization of a mixture of styrene and 1 3 butadiene gives SBR... 

Rubbers differ in their resistance to ozone. All the highly unsaturated rubbers (natural rubber, styrene-butadiene rubber, butyl rubber, nitrile rubber) are readily cracked while the deactivated double carbon-carbon bonds rubber (such as polychloroprene rubber) shows moderate ozone resistance. 

One of the most important solution blend polymers is high-styrene resin, which is manufactured by several companies worldwide. This is a latex blend of high-styrene rubber and normal styrene butadiene rubber. The different high-styrene master batches are available in the world as ... 

In a block copolymer, a long segment made from one monomer is followed by a segment formed from the other monomer. One example is the block copolymer formed from styrene and butadiene. Pure polystyrene is a transparent, brittle material that is easily broken polybutadiene is a synthetic rubber that is very resilient, but soft and opaque. A block copolymer of the two monomers produces high-impact polystyrene, a material that is a durable, strong, yet transparent plastic. A different formulation of the two polymers produces styrene-butadiene rubber (SBR), which is used mainly for automobile tires and running shoes, but also in chewing gum. 

FIGURE 22.11 Uniaxial stress-strain data (up-cycles) of solution-based styrene-butadiene rubber (S-SBR) samples with 60 phr silica at different prestrains s =100%, 150%, 200%, 250%, and 300% (symbols) and fittings (lines) with the stress-softening model Equations 22.19-22.24. The fitting parameters are indicated. The insert shows a magnification of the small-strain data. (From Kliippel, M. and Heinrich, G., Kautschuk, Gummi, Kunststojfe, 58, 217, 2005. With permission.)... 

FIGURE 26.20 The log a v speed function of the previous chart is combined with the friction master curves for a natural rubber (NR) and a styrene-butadiene rubber (SBR) gum compound on glass showing the limited range of friction values (and their position on the log a-iv axis for different testing conditions) which are obtained when the sliding speed is increased. 

FIGURE 26.52 Sliding abrasion of three different tread compounds as function of temperature at a sliding speed of 0.01 m/s (a) styrene-butadiene rubber (SBR), (b) ANR, (c) NR,-tread compound, —gum compound. 

FIGURE 26.64 Log (abrasion) for two tread compounds natural rubber (NR) + black and styrene-butadiene rubber (SBR) + black on two surfaces of different sharpness Alumina 60 and Alumina 180 blunt as function of log (energy dissipation). (From Grosch, K.A. and Heinz, M., Proc. IRC 2000, Helsinki, 2000, paper 48.)... 

FIGURE 27.9 T-peel strength values of styrene-butadiene rubber (SBS) treated with chloramine T aqueous solutions with different pH/waterbome polyurethane adhesive/roughened leather joints, as a function of the pH value of the chloramine T aqueous solutions. A adhesion failure to the rubber, M cohesive failure in tbe rubber. (From Navarro-Banon, M.V., Pastor-Bias, M.M., and Martm-Martinez, J.M., Proceedings of the 27th Adhesion Society, Wilmington, NC.)... 

Femandez-Garcfa J.C., Orgiles-Barcelo, and A.C., Martm-Martmez J.M., 1991, Halogenation of styrene-butadiene rubber to improve its adhesion to polyurethanes, J. Adhes. Sci Technol, 5, 1065-1080. Oldfield D. and Symes T.E.F., 1983, Surface modification of elastomers for bonding, J. Adhes., 16, 77-96. Pastor-Bias M.M., Ferrandiz-Gomez T.P., and Martm-Martmez J.M., 2000, Chlorination of vulcanized styrene-butadiene rubber using solutions of trichloroisocyanuric acid in different solvents, J. Adhes. Sci. Technol, 14, 561-581. 

As one of the most versatile copolymers in the world today, styrene-butadiene rubber is used in a number of different applications around the world. Some facts about the development of styrene-butadiene rubber and some of the products that are created with this strong and reliable synthetic rubber are described below. 

The Delta Mooney (A Mooney) test is an extension of the Mooney used on empirical grounds as a general indication of processibility for non-pigmented oil extended emulsion styrene/butadiene rubber. It quantifies the changes that occur in Mooney viscosity with time, either as the difference between viscosities recorded at two specified times or as the difference between the minimum viscosity recorded immediately after the commencement of the test and the subsequent maximum viscosity. Several alternative Delta Mooney values are defined depending on the times, whether minimum/maximum viscosity difference is used and whether or not the sample has been massed on a mill. Procedures for Delta Mooney are standardised in ISO 289-341, BS 903 Part A58-142 and in ASTM D334643. 

Order-disorder transitions and spinodals were computed for linear multi block copolymers with differing sequence distributions by Fredrickson et al. (1992). This type of copolymer includes polyurethanes, styrene-butadiene rubber, high impact polystyrene (HIPS) and acrylonitrile-butadiene-styrene (ABS) block copolymers. Thus the theory is applicable to a broad range of industrial thermoplastic elastomers and polyurethanes. The parameter... 

A list of typical commercial pervaporation membranes [23] is given in Table 3.1. Commercial hydrophilic membranes are very often made of polyvinyl alcohol (PVA), with differences in the degree of crosslinking. Commercial hydrophobic membranes often have a top layer in polydimethyl siloxane (PDMS). However, a wide variety of membrane materials for pervaporation can be found in the literature, including polymethylglutamate, polyacrylonitrile, polytetrafluoroethylene, polyvinylpyrrolidone, styrene-butadiene rubber, polyacrylic acid, and many others [24]. A comprehensive overview of membrane materials for pervaporation is given by Semenova et al. [25],... 

Mixing process Technical rubbers are blends of up to about 30 different compounds like natural rubber, styrene-butadiene rubber, silicate and carbon-black fillers, and mobile components like oils and waxes. These components show a large variety of physical, chemical, and NMR properties. Improper mixing leads to inhomogeneties in the final product with corresponding variations in mechanical and thermal properties (cf. Figure 7.4). 

Figure 14.1 ID spectra of a typical rubber, styrene-butadiene-rubber (SBR). a) Static spectrum acquired at a Larmor frequency of 500 MHz. The dipolar coupling is motionally averaged and different lines can be distinguished although they are still broadened by the residual dipolar couplings, b) MAS spectrum of the same sample at a MAS spinning frequency of 15 kHz. The line-broadening due to anisotropic spin interactions, e.g., residual dipolar couplings, is removed...

FIG. 18.3 Activation energy of diffusion as a function of Tg for 21 different polymers from low to high temperatures, ( ) odd numbers (O) even numbers 1. Silicone rubber 2. Butadiene rubber 3. Hydropol (hydrogenated polybutadiene = amorphous polyethylene) 4. Styrene/butadiene rubber 5. Natural rubber 6. Butadiene/acrylonitrile rubber (80/20) 7. Butyl rubber 8. Ethylene/propylene rubber 9. Chloro-prene rubber (neoprene) 10. Poly(oxy methylene) 11. Butadiene/acrylonitrile rubber (60/40) 12. Polypropylene 13. Methyl rubber 14. Poly(viny[ acetate) 15. Nylon-11 16. Poly(ethyl methacrylate) 17. Polyethylene terephthalate) 18. Poly(vinyl chloride) 19. Polystyrene 20. Poly (bisphenol A carbonate) 21. Poly(2,6 dimethyl-p.phenylene oxide). 

The free-radical kinetics described in Chapter 6 hold for homogeneous systems. They will prevail in well-stirred bulk or solution polymerizations or in suspension polymerizations if the polymer is soluble in its monomer. Polystyrene suspension polymerization is an important commercial example of this reaction type. Suspension polymerizations of vinyl ehloride and of acrylonitrile are described by somewhat different kinetic schemes because the polymers precipitate in these cases. Emulsion polymerizations aie controlled by still different reaetion parameters because the growing macroradicals are isolated in small volume elements and because the free radieals which initiate the polymerization process are generated in the aqueous phase. The emulsion process is now used to make large tonnages of styrene-butadiene rubber (SBR), latex paints and adhesives, PVC paste polymers, and other produets. 

When two different monomers are mixed and then polymerized, copolymers are formed. Depending on the ratio of the two monomers and the reaction conditions, the order of the units can range from quite regular (e.g., alternating) to completely random. In this way, polymers with a wide variety of properties can be produced. The most important rubber produced in the largest amount in the United States is styrene butadiene rubber (SBR), a polymer of styrene with butadiene in a 1 3 molecular ratio. 

The uses of mercaptans in polymers fall into three major categories chain transfer agents, additives such as stabilizers against heat or UV light, and monomers that incorporate an alkylmercapto group into their structure. Mercaptans r-dodecyl, n-dododecyl, etc. are excellent chain transfer agents used to control molecular weight of several different kinds of polymers, styrene butadiene rubber, acrylonitrile-butadiene-styrene, polyacrylates, to name a few. " " ... 

During the manufacturing process of styrene-butadiene rubber the polymerisation is stopped at a conversion rate of less than 90%. The residual monomers styrene and butadiene are removed by distillation. The odour-in-tensive compounds 4-phenylcyclohexene (from styrene and cis-butadiene) and 4-vinyl cyclohexene (from cis-butadiene and trans-butadiene) can be formed from the remaining monomers under the conditions of a thermally permitted Ti2s-t- 4s Diels-Alder cyclic addition. During indoor air measurements, carried out in six different office rooms in each case 3 days after new carpets had been laid, concentrations of 4-phenylcyclohexene of 29-45 pg m could be ascertained. It is suspected that the emission of the trimer of 2-methyl-l-propene from a glued carpet is also caused by chemical reaction. 

Of particular importance for detection of chemical or physical change in polymer materials are mobility filters, which are sensitive to differences in the numbers of molecules within a given window of correlation times. Within reasonable approximation such filters are relaxation filters. Here, Tj filters are sensitive to differences in the fast motion regime while T2 and Tip filters are sensitive to the slow motion regime. Which time window is of importance can be seen from Fig. 5.7 [101]. It shows a double-logarithmic plot of the mechanical relaxation strengths Hi(t) for two carbon-black filled styrene-butadiene rubber (SBR) samples as a function of the mechanical relaxation time T. They have been measured by dynamic mechanical relaxation spectroscopy. In terms of NMR, the curves correspond to spectral densities of motion. But the spectral densities relevant to NMR are mainly those referring... 

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