Rheology elastomers

The net effect is that tackifiers raise the 7g of the blend, but because they are very low molecular weight, their only contribution to the modulus is to dilute the elastic network, thereby reducing the modulus. It is worth noting that if the rheological modifier had a 7g less than the elastomer (as for example, an added compatible oil), the blend would be plasticized, i.e. while the modulus would be reduced due to network dilution, the T also would be reduced and a PSA would not result. This general effect of tackification of an elastomer is shown in the modulus-temperature plot in Fig. 4, after the manner of Class and Chu. Chu [10] points out that the first step in formulating a PSA would be to use Eqs. 1 and 2 to formulate to a 7g/modulus window that approximates the desired PSA characteristics. Windows of 7g/modulus for a variety of PSA applications have been put forward by Carper [35]. 

This mbber is very tacky in nature and contains acrylic group, which makes it polar in nature. Nanocomposites have been prepared based on this elastomer with a wide range of nanohllers. Layered silicates [53-55] have been used for this preparation. Sol-gel method [56,57], in situ polymerization [58], and nanocomposites based on different clays like bentonite [59] and mica [60] have been described. The mechanical, rheological, and morphological behaviors have been investigated thoroughly. 

Veenstra H., Hoogvfiet R.M., Norder B., De B., and Abe P. Microphase separation and rheology of a semicrystalUne poly(ether-ester) multiblock copolymer, J. Polym. Sci. B. Polym Phys., 36, 1795, 1998. Garbrieelse W., SoUman M., and Dijkstra K., Microstmcture and phase behaviour of block copolyfether ester) thermoplastic elastomers. Macromolecules, 34, 1685, 2001. 

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. 

Such soft-touch materials are usually TP Vs or thermoplastic elastomers (TPEs) which combine the moldability of thermoplastics in the melt state with elasticity, lower hardness, fracture resistance, and surface characteristics of elastomers. However, plastics and elastomers respond differently to mechanical stress. Hence, both rheological behavior and mechanical strength will to a large extent depend on the morphology of the blend which may change with change in the composition. 

Wang, W. and Zheng, Q. The Dynamic Rheological Behavior and Morphology of Nylon/Elastomers Blends, J. Mater. Set Lett. 40, 2005. 

Medintseva, T.I., Dreval, V.E., Erina, N.A., and Prut, E.V., Rheological properties thermoplastic elastomers based on isotactic polypropylene with an ethylene-propylene-diene terpolymer, Polym. Sci. A, 45, 2032, 2003. 

J.L. Leblanc, Elastomer—filler interactions and the rheology of filled mbber compounds, J. Appl. Polym. ScL, 78, 1541-1550, 2000. 

A convenient term for the rheological properties of an unvulcanised elastomer (see Rheology). It has been defined as the susceptibility to, and retentivity of deformation , and also the degree of flow which takes place under given conditions of temperature and pressure . The use of the term viscosity is a more appropriate description. Plasticity Retention Index... 

Nomenclature, 17 384-413 basic scheme of, 17 384-385 biochemical, 17 401-402 computerized approaches to, 17 400-401 elastomer, 21 761t enzyme, 10 258-260 for ionic liquids, 26 840-841 glossaries related to, 17 404 inorganic, 17 387-394 macromolecular (polymers), 17 403 404 organic, 17 394-401 polymer, 20 390-395 pump, 21 88 quinone, 21 236-237 reactor technology, 21 358 related to mass transfer, 15 731-737 reverse osmosis, 21 674-676 Society of Rheology, 21 704 spray-related, 23 199t systematic, 17 394... 

There are three situations that appear to be relevant here. First, we may think of a solid polymer formed from the melt second, the much more compliant elastomers that initially come to mind when we think of rubber elasticity and third, polymer gels formed in polymer solutions. In each case the details of the physical chemistry of the macromolecules is crucial to the understanding of the structure that is formed. In this section we will concentrate on organic macromolecules because the rheology of these molecular systems is often the reason for their use. 

At temperatures above the Tg, bitumens generally show Newtonian behavior. Below the Tg bitumens have rheological properties similar to elastomers. 

Polymers are viscoelastic materials meaning they can act as liquids, the visco portion, and as solids, the elastic portion. Descriptions of the viscoelastic properties of materials generally falls within the area called rheology. Determination of the viscoelastic behavior of materials generally occurs through stress-strain and related measurements. Whether a material behaves as a viscous or elastic material depends on temperature, the particular polymer and its prior treatment, polymer structure, and the particular measurement or conditions applied to the material. The particular property demonstrated by a material under given conditions allows polymers to act as solid or viscous liquids, as plastics, elastomers, or fibers, etc. This chapter deals with the viscoelastic properties of polymers. 

Freitas LDL, Stadler R. Thermoplastic elastomers by hydrogen bonding. 3. Interrelations between molecular parameters and rheological properties. Macromolecules 1987 20 2478-2485. 

Suhara, F., and S. K. N. Kutty, Rheological properties of short polyester fiber-polyurethane elastomer composite with different interfacial bonding agents, Polym. Plast. Technol. Eng., 37(1), 57 (1998). 

There is a growing interest in the synthesis of star-block thermoplastic elastomers (TPEs) on account of their unique mechanical and rheological properties [71-73]. PIB-based TPEs exhibit excellent mechanical properties and have superior thermal and oxidative stabiHties relative to polydiene-based TPEs [73,74]. 

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