By Evaristo Riande, Ricardo Diaz-Calleja, Margarita Prolongo, Rosa Masegosa, Catalina Salom
Offers a accomplished and systematic account of the responses of macromolecular fabrics to mechanical strength fields, showcasing important engineering functions to brief and dynamic perturbations of macromolecular fabrics, and viscoelastic parameters that situation the NonNewtonian habit of polymers. DLC: Polymers--Viscosity.
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Additional info for Polymer viscoelasticity: stress and strain in practice
15) given that thecosine of the angle formed by two vectors -1 with equal probability and in average ca ) = 0 except wheni =j ; In thatcase the scalar product is equal to In general, it can be shownthat the statistical distribution of end-to-end distances of a chain, independently of what its geometry might be, can be Chapter I 24 represented by a Gaussian distribution function if the number of segments of the chain is sufficiently large, in order to guarantee that the correlation between bonds is totally lost over the length of the chain.
2): For many polymers, a narrow distribution of molecular weight leads to better properties than a wide distribution. n S t r u ~ t ~ of r e Polymers 13 The properties of polymer materials do not just depend on their chemical composition and molecular weight. Their molecular structure also has a markedinfluenceon their physical properties. “Molecular structure” is understood to mean the arrangement of the atoms in the molecule. The term “configuration” refers to the organization of the atoms along the chain; to change a polymer configuration it is necessary to break and reform chemical or primary bond (3).
In the crystallization of polymers starting from very dilute solutions (concentrations less than l%), polymer single crystals are generated by cooling or by additio? of a precipitant. Single crystals have the shape of lamellae about 100 A thick and severalmicrometers in length (see Fig. 6) (6). The general characteristic of single crystals is their small size in comparison withthe crystal size of small molecules, whichlimits their study by X-rays. The orientation of the chains in the lamellae, determined by electron diffraction, shows that the chains are nearly normal to the lamellar surface.