Polybutadiene glass

Wide-line H FID and relaxation measurements of a relatively simple motionally heterogeneous system, the triblock copolymer styrene-butadiene-styrene, have been performed in a temperature range between the polystyrene and polybutadiene glass transition temperatures. The two FID and the two Tip components found at each temperature have been correlated by means of a 2D approach. It is shown that this approach allows dynamic information, not accessible simply by interpreting proton Ti and Tip data, to be revealed. In the case examined, the correlation found could be confirmed by high-resolution H... 

Figure 3.15 Intrinsic adhesive fracture energy, Go, for polybutadiene/glass interfaces versus the fraction of vinylsilane in the mixture of vinyl and ethyl silanes used to treat the glass substrate surface [123].

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. 

The glass-transition temperature in amorphous polymers is also sensitive to copolymerization. Generally, T of a random copolymer falls between the glass-transition temperatures of the respective homopolymers. For example, T for solution-polymerized polybutadiene is —that for solution-polymerized polystyrene is -HlOO°C. A commercial solution random copolymer of butadiene and styrene (Firestone s Stereon) shows an intermediate T of —(48). The glass-transition temperature of the random copolymer can sometimes be related simply as follows ... 

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. 

Prepa.ra.tion, The preparation of amorphous high (99%) 1,2-polybutadiene was first reported iu 1981 (27). The use of a heterocycHc chelating diamine such as dipiperidine ethane iu the polymerization gave an amorphous elastomeric polymer of 99.9% 1,2 units and a glass-transition temperature of +5°C. In a previous description (53,54) of the use of a chelating diamine such as A/A/N(N -tetramethylethylene diamine, an 80% 1,2-polybutadiene with a glass-transition temperature of —30°C was produced. 

Inclusion of double bonds will stiffen the chain at the point of inclusion but at the same time may increase the flexibility of adjacent bonds. The net effect may therefore be to reduce the glass transition temperature and this appears to occur in 1,4-polybutadiene when compared with polyethylene. 

The glass transition temperatures (Tg) of both modified and unmodified PSs were determined by DSC analysis, and thermomechanic analysis was controlled by TMK. The results are given in Table 8. It is seen from Table 8 that the highest glass transition temperature (410 K) was obtained with chlorohydrinated PS and that of the lowest (370 K) with olefinic PS. The lowest glass transition temperature in the alkenylated PS caused to elasticity properties on polybutadien and polyisopren fragments. 

TDI isomers, 210 Tear strength tests, 242-243 TEDA. See Triethylene diamine (TEDA) Telechelic oligomers, 456, 457 copolymerization of, 453-454 Telechelics, from polybutadiene, 456-459 TEM technique, 163-164 Temperature, polyamide shear modulus and, 138. See also /3-transition temperature (7)>) Brill temperature Deblocking temperatures //-transition temperature (Ty) Glass transition temperature (7) ) Heat deflection temperature (HDT) Heat distortion temperature (HDT) High-temperature entries Low-temperature entries Melting temperature (Fm) Modulu s - temperature relationship Thermal entries Tensile strength, 3, 242 TEOS. See Tetraethoxysilane (TEOS)... 

Reactive compatibilization can also be accomplished by co-vulcanization at the interface of the component particles resulting in obliteration of phase boundary. For example, when cA-polybutadiene is blended with SBR (23.5% styrene), the two glass transition temperatures merge into one after vulcanization. Co-vulcanization may take place in two steps, namely generation of a block or graft copolymer during vulcanization at the phase interface and compatibilization of the components by thickening of the interface. However, this can only happen if the temperature of co-vulcanization is above the order-disorder transition and is between the upper and lower critical solution temperature (LCST) of the blend [20]. 

Liquid rubbers In order to improve the flexibihty of short glass fiber-reinforced epoxy composites, Kaynak et al. [53] modified the epoxy resin matrix with hydroxyl-terminated polybutadiene (HTPB) liquid mbber. A silane coupling agent was also used to improve the interfacial adhesion between glass fibers and epoxy matrix. However, Humpidge et al. [54] reported some unique processing problems for the resulting pasty mixmres when short textile fibers were incorporated in a hquid mbber medium. 

One characteristic of shear banded flow is the presence of fluctuations in the flow field. Such fluctuations also occur in some glassy colloidal materials at colloid volume fractions close to the glass transition. One such system is the soft gel formed by crowded monodisperse multiarm (122) star 1,4-polybutadienes in decane. Using NMR velocimetry Holmes et al. [23] found evidence for fluctuations in the flow behavior across the gap of a wide gap concentric cylindrical Couette device, in association with a degree of apparent slip at the inner wall. The timescale of these fluctuations appeared to be rapid (with respect to the measurement time per shear rate in the flow curve), in the order of tens to hundreds of milliseconds. As a result, the velocity distributions, measured at different points across the cell, exhibited bimodal behavior, as apparent in Figure 2.8.13. These workers interpreted their data... 

The polybutadienes prepared with these barium t-butoxide-hydroxide/BuLi catalysts are sufficiently stereoregular to undergo crystallization, as measured by DTA ( 8). Since these polymers have a low vinyl content (7%), they also have a low gl ass transition temperature. At a trans-1,4 content of 79%, the Tg is -91°C and multiple endothermic transitions occur at 4°, 20°, and 35°C. However, in copolymers of butadiene (equivalent trans content) and styrene (9 wt.7. styrene), the endothermic transitions are decreased to -4° and 25°C. Relative to the polybutadiene, the glass transition temperature for the copolymer is increased to -82°C. The strain induced crystallization behavior for a SBR of similar structure will be discussed after the introduction of the following new and advanced synthetic rubber. 

Figure 2. Glass transition temperature from DSC in cross-linked polybutadiene as a function of...

Sodium phosphate(s), 28 831-834, 29 18 carbon dioxide by-product of manufacture, 4 810 economic aspects of, 28 860 uses for, 28 833-834 Sodium polybutadiene, 9 555, 556 Sodium polymetaphosphate, 8 416 Sodium polyphosphates, 9 16 manufacture of, 28 858 Sodium polyphosphate glass, 28 851 Sodium polystyrene sulfonate cosmetic surfactant, 7 835t Sodium polysulfide(s), 23 640 in sodium production, 22 773 Sodium-potassium eutectic, 15 252... 

Investigation on the Dynamics of Polybutadiene Near the Glass Transition. 

Dependence of the Nonergodicity Parameter in Polybutadiene in the Neighborhood of the Glass Transition. 

The method is based on the fact that the rate of conformational change required for excimer formation depends on the free volume induced by the segmental motions of the polymer occurring above the glass transition. DIPHANT (compound 3 in Figure 8.3) was used as an excimer-forming probe of three polymer samples consisting of polybutadiene, polyisoprene and poly(dimethylsiloxane).a)... 

Figure B8.2.1 shows the fluorescence spectra of DIPHANT in a polybutadiene matrix. The h/lu ratios turned out to be significantly lower than in solution, which means that the internal rotation of the probe is restricted in such a relatively rigid polymer matrix. The fluorescence intensity of the monomer is approximately constant at temperatures ranging from —100 to —20 °C, which indicates that the probe motions are hindered, and then decreases with a concomitant increase in the excimer fluorescence. The onset of probe mobility, detected by the start of the decrease in the monomer intensity and lifetime occurs at about —20 °C, i.e. well above the low-frequency static reference temperature Tg (glass transition temperature) of the polybutadiene sample, which is —91 °C (measured at 1 Hz). This temperature shift shows the strong dependence of the apparent polymer flexibility on the characteristic frequency of the experimental technique. This frequency is the reciprocal of the monomer excited-state...

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