Elastic block

Another example is even older the thermoplastic elastomers based on polyurethane their chains contain a number of blocks, altematingly hard and soft PU blocks, (elastic yarns, such as Lycra and Spandex ). 

Prolyl Hydroxylation Blocks Elastic Fiber Formation In Vitro and In Vivo... 

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. 

The argument, at its simplest, is as follows. The primary function of a spring is that of storing elastic energy and - when required - releasing it again. The elastic energy stored per unit volume in a block of material stressed uniformly to a stress a is ... 

By linking the chain ends of different molecules they form a type of network structure as long as the domains remain glassy. As the polymer is heated above the of the domain polymer block the domain molecules become mobile and on application of a stress the material flows like a thermoplastic. On cooling, new domains will be formed, thus regenerating the elastic state. 

In 1978 Hiils (Mumcu et al ) described the properties of a block copolymer prepared by condensation of polytetramethylene ether glycol with laurin lactam and decane-1,10-dicarboxylic acid. The materials were introduced as XR3808 and X4006. The polyamide XR3808 is reported to have a specific gravity of 1.02, a yield stress of 24 MPa, a modulus of elasticity of 300 MPa and an elongation of break of 360%. The Swiss company Emser Werke also introduced similar... 

Various elastic elements are added to disposable sanitary products. Strands of lycra, natural rubber, polyurethane foam, and other elastic laminates are applied to provide good fit and avoid leakage. These are attached with adhesives. While non-PSA formulas such as polybutene-based [64] and polyamide [65] adhesives have shown utility, as well as benefits in terms of resistance to baby oils and lotions, adhesives based on styrenic block copolymers still dominate. SBC-based... 

Classical lamination theory consists of a coiiection of mechanics-of-materials type of stress and deformation hypotheses that are described in this section. By use of this theory, we can consistentiy proceed directiy from the basic building block, the lamina, to the end result, a structural laminate. The whole process is one of finding effective and reasonably accurate simplifying assumptions that enable us to reduce our attention from a complicated three-dimensional elasticity problem to a SQlvable two-dimensinnal merbanics of deformable bodies problem. 

Since the increase of the elastic modulus of oriented polymers with draw ratio is, to a large extent, the consequence of the tie molecules or intercrystalline bridges interconnecting crystal blocks within the fibrils 72) one may anticipate a correlation to exist between indentation anisotropy and modulus. Recent data 23) illustrating the... 

Anionic polymerization of pivalolactone with the polystyrene anion produced only homopolymer mixtures, but the polystyrene carboxylate anion was able to give a block copolymer336. The block efficiency depends on catalyst ratio and conversion because the initiation step is slow compared with propagation337. Tough and elastic films were obtained by graft copolymerization or block copolymerization of pivalolactone onto elastomers containing tetrabutylammonium carboxylate groups338,339. ... 

Furthermore, as discussed in Section 6.7, the ability of the elastic d orbitals to function as electron sinks contributes greatly to the rich variety of redox chemistry that is so characteristic of the cf-block elements. Here too, therefore, we recognize the bonding role of the d orbitals in Werner-type complexes as well as in carbonyl-type chemistry. 

For a rectangular rubber block, plane strain conditions were imposed in the width direction and the rubber was assumed to be an incompressible elastic solid obeying the simplest nonhnear constitutive relation (neo-Hookean). Hence, the elastic properties could be described by only one elastic constant, the shear modulus jx. The shear stress t 2 is then linearly related to the amount of shear y [1,2] ... 

The above equations gave reasonably reliable M value of SBS. Another approach to modeling the elastic behavior of SBS triblock copolymer has been developed [202]. The first one, the simple model, is obtained by a modification of classical rubber elasticity theory to account for the filler effect of the domain. The major objection was the simple application of mbber elasticity theory to block copolymers without considering the effect of the domain on the distribution function of the mbber matrix chain. In the derivation of classical equation of rabber elasticity, it is assumed that the chain has Gaussian distribution function. The use of this distribution function considers that aU spaces are accessible to a given chain. However, that is not the case of TPEs because the domain also takes up space in block copolymers. 

The new polymers are intermediate in composition and crystallinity between the essentially amorphous EPR and the semicrystalhne iPP. The presence of the complementary blocks of elastomers for both ethylene and propylene crystallinity should not indicate a similarity, beyond the levels of the crystallinity in the properties of the E-plastomers and the P-plastomers. The E-plastomers and the P-plastomers differ in their stmctural, rheological, as well as their thermal, mechanical, and elastic properties. In a comparison of the tensile strength and tensile recovery (tension set) from a 100% elongation for a range of P-plastomers and E-plastomers, the former have lower tension set than EPR and iPP. However, for comparative E-plastomers and P-plastomers at equivalent tensile strength, the latter have significantly better tension set. In summary, P-plastomers are tough polyolefins which are uniquely soft and elastic. 

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