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Polymers, chain type amorphous material

The answers to these questions can be gleaned from Table 13-2, which compares approximate values of the tensile modulus for various polymers. Rubbers or elastomer are also amorphous, of course, but they respond to a stress in an entirely different manner to all other types of materials. Because they have low Ts, at ordinary temperatures, they respond to a load by changing their distribution of chain conformations, the chains becoming more extended as the material is stretched. A rubber has to be extended many limes its original dimensions before the covalent bonds take the load. We will consider rubber elasticity as a separate topic later. [Pg.413]

In spin-diffusion studies it is possible to detect not only two but three domain sizes. The third domain can be considered the interface (i) between the other two domains, which can be different chemical species in a polymer blend or rigid crystalline (r) and mobile amorphous (m) material in a semicrystalline polymer. To illustrate this point, a mobility timescale is depicted in Fig. 7.2.25(a) and the simplified ID domain structure of PE underneath in (b). Rigid crystalline and mobile amorphous materials exhibit motion of chain segments with different correlation times Tc. The chains at the interface between both domains exhibit intermediate mobility. The exact ranges of correlation times in the individual domains depend on the particular choice of filters. Therefore, the values of domain sizes derived through spin-diffusion NMR also depend on the type of filters used. In particular, the interface is defined solely by the NMR experiment and can only be detected if the filters are properly chosen. [Pg.299]

Viswanathan et al., 1999). Some chapters in this book deal with this fascinating research topic. Features of this phenomenon can be summarized as follows (i) The film material transfer occurs over micrometer distances, far beyond the dimension of single polymer chain, are achieved, and (ii) the inscribed rehef can be erased by heating above a softening temperature or uniform irradiation of circularly polarized light (CPL). Most of the polymers employed for these studies possess a push-pull type Az unit such as Disperse Red 1, and the physical state is amorphous in nature with no particular regular structure in the film (Fig. 8.9). Other characteristics are further listed in Table 8.1. Most investigations have... [Pg.283]

The available range of membrane materials includes polymeric, carbon, silica, zeolite and other ceramics, as well as composites. Each type of membrane can have a different porous structure, as illustrated in Figure 5.2. Membranes can be thought of as having a fixed (immovable) network of pores in which the gas molecule travels, with the exception of most polymeric membranes [28,44]. Polymeric membranes are composed of an amorphous mix of polymer chains whose interactions involve mostly van der Waals forces. However, some polymers reveal a behaviour that is consistent with the idea of existence of opened pores within their matrix. This is especially true for high free volume, high... [Pg.90]

TPO materials are defined as compounds (mixtures) of various polyolefin polymers, semicrystalline thermoplastics, and amorphous elastomers. Most TPOs are composed of polypropylene and a copolymer of ethylene and propylene called ethylene—propylene rubber (EPR) [2]. A common rubber of this type is called ethylene propylene diene monomer rubber (EPDM), which has a small amount of a third monomer, a diene (two carbon-carbon double bonds in it). The diene monomer leaves a small amount of unsaturation in the polymer chain that can be used for sulfur cross-linking. Like most TPEs, TPO products are composed of hard and soft segments. TPO compounds include fillers, reinforcements, lubricants, heat stabilizers, antioxidants, UV stabilizers, colorants, and processing aids. They are characterized by high impact strength, low density, and good chemical resistance they are used when durability and reliability are primary concerns. [Pg.381]

As is typical with most thermoplastic materials, the main properties of PP in the melt state are derived from the average length of the polymer chains and the breadth of the distribution of the polymer chain lengths in a given product. In the solid state, the main properties of the PP material reflect the type and amount of crystalline and amorphous regions formed from the polymer chains. [Pg.15]


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