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Tensile strength networks

When the void space in an agglomerate is completely filled with a Hquid (Fig. Ic), the capillary state of wetting is reached, and the tensile strength of the wet particle matrix arises from the pressure deficiency in the Hquid network owing to the concave Hquid interfaces at the agglomerate surface. This pressure deficiency can be calculated from the Laplace equation for chcular capillaries to yield, for Hquids which completely wet the particles ... [Pg.110]

Blends with styrenic block copolymers improve the flexibiUty of bitumens and asphalts. The block copolymer content of these blends is usually less than 20% even as Httie as 3% can make significant differences to the properties of asphalt (qv). The block copolymers make the products more flexible, especially at low temperatures, and increase their softening point. They generally decrease the penetration and reduce the tendency to flow at high service temperatures and they also increase the stiffness, tensile strength, ductility, and elastic recovery of the final products. Melt viscosities at processing temperatures remain relatively low so the materials are still easy to apply. As the polymer concentration is increased to about 5%, an interconnected polymer network is formed. At this point the nature of the mixture changes from an asphalt modified by a polymer to a polymer extended with an asphalt. [Pg.19]

Vulcanization changes the physical properties of rubbers. It increases viscosity, hardness, modulus, tensile strength, abrasion resistance, and decreases elongation at break, compression set and solubility in solvents. All those changes, except tensile strength, are proportional to the degree of cross-linking (number of crosslinks) in the rubber network. On the other hand, rubbers differ in their ease of vulcanization. Since cross-links form next to carbon-carbon double bonds. [Pg.638]

FIGURE 18.2 Tensile strength of styrene-butadiene rubber (SBR) as a function of network chain density. (From Bueche, F. and Dudek, T.J., Rubber Chem. Tech., 36, 1, 1963.)... [Pg.520]

This changing of the path of crack propagation gives the material the better resistant characters for fracture. The same type of phenomenon occurs in the materials filled with fibers. Fibers play the same role more clearly on reinforcing the materials and make the tensile strength much higher. Thus, surely we can expect that the strand of molecules and the super-networks work in the same manner in the carbon black-hlled mbber, which will be discussed in detail later. [Pg.530]

Figure 18.17 shows that the characteristics of the stress-strain curve depend mainly on the value of n the smaller the n value, the more rapid the upturn. Anyway, this non-Gaussian treatment indicates that if the rubber has the idealized molecular network strucmre in the system, the stress-strain relation will show the inverse S shape. However, the real mbber vulcanizate (SBR) that does not crystallize under extension at room temperature and other mbbers (NR, IR, and BR at high temperature) do not show the stress upturn at all, and as a result, their tensile strength and strain at break are all 2-3 MPa and 400%-500%. It means that the stress-strain relation of the real (noncrystallizing) rubber vulcanizate obeys the Gaussian rather than the non-Gaussian theory. [Pg.532]

When the butyl rubber was compounded with up to 30 percent of polyisobutylene, which, lacking the unsaturated isoprene units, did not enter into the cross-linking reaction, the tensile strengths were, of course, considerably reduced. They were found nevertheless to be accurately represented by the same equation, (53), provided merely that Sa is taken as the fraction of the composite specimen consisting of network chains subject to orientation. Thus, in this case... [Pg.485]

The distribution of the thi monomer in molecular chains or in the whole polymer should affect the perfection of the vulcanizate network, free chain ends or the uncross-linked parts in the polymer making no contribution to the tensile strength but acting as a plasticizer of like structure as the polymer. [Pg.202]

Vj g-EPDM and VOCI3-EPDM vulcanizate tensile strength Is not simply explainable by network quality resulting from difference In the third monomer distribution in the terpolymers. [Pg.208]

Collagens (see p. 344), of which there are at least 19 different varieties, form fibers, fibrils, networks, and ligaments. Their characteristic properties are tensile strength and flexibility. Elastin is a fiber protein with a high degree of elasticity. [Pg.346]

The maximum tensile strength of the pseudo-IPNs appeared at about the 80 20 ratio of PU/VMCC for both pseudo-IPNs with and without opposite charge groups. Presumably the maximum entangle-ment between the VMCC chains and the PU network also occurred at this composition ( Figure 1). ... [Pg.316]


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See also in sourсe #XX -- [ Pg.80 , Pg.172 , Pg.173 , Pg.177 ]




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Experimental Results on the Relationship between Tensile Strength and Network Structure

Tensil strength

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