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Tensile strength blends

Polybutadiene Higher resilience than similar natural rubber compounds, good low-temperature behavior and adhesion to metals, but poor tear resistance, poor tack, and poor tensile strength Blends with natural rubber and SBR manufacture of high-impact polystyrene... [Pg.420]

Most of the polymer s characteristics stem from its molecular stmcture, which like POE, promotes solubiUty in a variety of solvents in addition to water. It exhibits Newtonian rheology and is mechanically stable relative to other thermoplastics. It also forms miscible blends with a variety of other polymers. The water solubiUty and hot meltable characteristics promote adhesion in a number of appHcations. PEOX has been observed to promote adhesion comparable with PVP and PVA on aluminum foil, cellophane, nylon, poly(methyl methacrylate), and poly(ethylene terephthalate), and in composite systems improved tensile strength and Izod impact properties have been noted. [Pg.320]

Copolymers of S-caprolactone and L-lactide are elastomeric when prepared from 25% S-caprolactone and 75% L-lactide, and rigid when prepared from 10% S-caprolactone and 90% L-lactide (47). Blends of poly-DL-lactide and polycaprolactone polymers are another way to achieve unique elastomeric properties. Copolymers of S-caprolactone and glycoHde have been evaluated in fiber form as potential absorbable sutures. Strong, flexible monofilaments have been produced which maintain 11—37% of initial tensile strength after two weeks in vivo (48). [Pg.192]

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]

This lower has a number of ramifications on the properties of polybutadiene. For example, at room temperature polybutadiene compounds generally have a higher resilience than similar natural rubber compounds. In turn this means that the polybutadiene rubbers have a lower heat build-up and this is important in tyre applications. On the other hand, these rubbers have poor tear resistance, poor tack and poor tensile strength. For this reason, the polybutadiene rubbers are seldom used on their own but more commonly in conjunction with other materials. For example, they are blended with natural rubber in the manufacture of truck tyres and, widely, with SBR in the manufacture of passenger car tyres. The rubbers are also widely used in the manufacture of high-impact polystyrene. [Pg.291]

Although the elastomer phase is essentially in particulate form, the tensile strength of the blend can be increased five-fold by increasing the cross-link density from zero to that conventionally used in vulcanisation processes, whilst tension set may be reduced by over two-thirds. Since the thermoplastic polyolefin phase may be completely extracted by boiling decalin or xylene, there is apparently no covalent chemical bonding of elastomer and thermoplastic phases. [Pg.303]

A high-impact polystyrene (polystyrene SBR blend) may have seven times the impact strength of ordinary polystyrene, but about half the tensile strength, a lower hardness and a softening point some 15°C lower. Because of the rubber content there may be a reduction in light and heat stability and stabilisers are normally incorporated. [Pg.439]

Spandex fibres, because of their higher modulus, tensile strength and resistance to oxidation, as well as their ability to be produced at finer deniers, have made severe inroads into the natural rubber latex thread market. They have also enabled lighter weight garments to be produced. Staple fibre blends with non-elastic fibres have also been introduced. [Pg.791]

Heat treatment of TPU after its synthesis could increase its molecular weight, thus increase the strength of the blending products. It also decreases the hardness of the products. For example, the polymer blends from PVC and 881014TPU, a TPU made in our lab, showed a 10% increase in its tensile strength and 5% increase in its elasticity when the TPU was treated at 105°C for 7-9 hours compared with no treatment. [Pg.139]

Figure 6 Tensile strength versus percent polypropylene in SBR ionomer/PP blends. Figure 6 Tensile strength versus percent polypropylene in SBR ionomer/PP blends.
As another example, a synergistic enhancement of tensile strength has been reached in blends of a sulfo-nated polyacrylonitrile terpolymer (SPAN) with a polyurethane (PU) cationomer [23]. Maximum enhancement was achieved at a blend composition of 30/70 (PU/ SPAN). At this blend composition, the tensile strength was raised from an initial value of 78.5 MPa to 196 MPa and the strain-to-fracture was at its highest. The en-... [Pg.151]

Figure 8 Tensile strength versus ionomer content (wt%) for a blend of an Na-SPS ionomer (5.26 mol%) and PS. Figure 8 Tensile strength versus ionomer content (wt%) for a blend of an Na-SPS ionomer (5.26 mol%) and PS.
A new process to develop interface vulcanization is grafting of selective accelerators onto a polymer chain, which in the subsequent process of vulcanization acts as an effective cure accelerator for the second polymer component in the blend. Beniska et al. [6] prepared SERFS blends where the polystyrene phase was grafted with the accelerator for curing SBR. Improved hardness, tensile strength, and abrasion resistance were obtained. Blends containing modified polystyrene and rw-1,4-polybutadiene showed similar characteristics as SBS triblock copolymers. [Pg.464]

To introduce some interfacial physico-chemical linkage between EVA and PRP, blends were made by adding different quantities of M AH-PP. Some results are demonstrated in Table 12, The physico-mechanical properties of the PRP-EVA compositions modified with MAH-PP showed that properties are influenced by MAH-PP concentration. Compositions with better impact strength and improved brittleness can be prepared by varying the modifier concentration. Tensile strength and elongation are not significantly influenced by the addition of a modifier. An increase in the modifier con-... [Pg.473]

Figure 15 (A) Tensile strength versus draw ratio of nylon 46-Vectra B (75 25 wt ratio) and (B) tensile modulus of the blends when 2.7 wt% of SA-g-EPDM was added. Lines are guides for eyes. Closed symbols are mechanical properties of the binary nylon 46-Vectra B blend (75 25 wt ratio) Source Ref. 57. Figure 15 (A) Tensile strength versus draw ratio of nylon 46-Vectra B (75 25 wt ratio) and (B) tensile modulus of the blends when 2.7 wt% of SA-g-EPDM was added. Lines are guides for eyes. Closed symbols are mechanical properties of the binary nylon 46-Vectra B blend (75 25 wt ratio) Source Ref. 57.
The effect of ionomer concentration on the mechanical properties of PP-EPDM blends is given Table 9. It is seen that the tensile strength and modulus show a maximum at 5 wt% of both ionomer A and B, thereafter, it decreases at higher ionomer loading. The properties are higher for ternary blends containing ionomer B than these containing ionomer A. On the other hand, addition... [Pg.641]

Composition of blend (ABS-rich) Yield tensile strength, cry (MPa) Elongation at break, EB (%)... [Pg.643]

Compatibility and various other properties such as morphology, crystalline behavior, structure, mechanical properties of natural rubber-polyethylene blends were investigated by Qin et al. [39]. Polyethylene-b-polyiso-prene acts as a successful compatibilizer here. Mechanical properties of the blends were improved upon the addition of the block copolymer (Table 12). The copolymer locates at the interface, and, thus, reduces the interfacial tension that is reflected in the mechanical properties. As the amount of graft copolymer increases, tensile strength and elongation at break increase and reach a leveling off. [Pg.644]

The mechanical properties of these blends are also increased with an increase in compatibilizer concentration. The improvement in tensile strength and tear strength on the addition of modified polyolefins are shown in Fig. 15. The mechanical properties also show a leveling off after the optimum concentration. The im-... [Pg.681]


See other pages where Tensile strength blends is mentioned: [Pg.265]    [Pg.48]    [Pg.44]    [Pg.265]    [Pg.48]    [Pg.44]    [Pg.331]    [Pg.239]    [Pg.330]    [Pg.418]    [Pg.421]    [Pg.421]    [Pg.272]    [Pg.272]    [Pg.58]    [Pg.487]    [Pg.184]    [Pg.186]    [Pg.485]    [Pg.555]    [Pg.5]    [Pg.304]    [Pg.931]    [Pg.444]    [Pg.150]    [Pg.151]    [Pg.590]    [Pg.597]    [Pg.598]    [Pg.640]    [Pg.642]   


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Tensil strength

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