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Supermolecular Morphology

With these recent developments in molecular morphology, supermolecular structure and properties attention needs to be redirected to a molecular understanding of the crystallization mechanism. From this will stem naturally our understanding of the morphology and properties. A well developed phenomenological base has already been established . Unfortunately, it does not lead to a unique molecular interpretation. The development of molecular models for the kinetic processes are in the early stages of development and must await the tests of time and experiment to attest their validity. We must remember that the basic reason for the formation of the lamella-like crystallites has not as yet been firmly established . [Pg.119]

The molecular stmcture of the copolymers is also important. Molecular-weight measurements (osmometry, gpc) and functional group analysis are useful. Block copolymers require supermolecular (morphological) stmctural information as well. A listing of typical copolymer characterization tools and methods is shown in Table 6. [Pg.187]

Figure 15 Morphological map of linear polyethylene fractions. Plot of molecular weight against crystallization temperature. The types of supermolecular structures are represented by symbols. Patterns a, b and c represent spherulitic structures with deteriorating order from a to c. Patterns g and d represent rods or sheet-like structures whose breadth is comparable to their length g or display a different aspect ratio d. Pattern h represents randomly oriented lamellae. Neither h nor g patterns have azimuthal dependence of the scattering. Reproduced with permission from Ref. [223]. Copyright 1981 American Chemical Society. (See Ref. [223] for full details.) Note the pattern a is actually located as o in the figure this was an error on the original. Figure 15 Morphological map of linear polyethylene fractions. Plot of molecular weight against crystallization temperature. The types of supermolecular structures are represented by symbols. Patterns a, b and c represent spherulitic structures with deteriorating order from a to c. Patterns g and d represent rods or sheet-like structures whose breadth is comparable to their length g or display a different aspect ratio d. Pattern h represents randomly oriented lamellae. Neither h nor g patterns have azimuthal dependence of the scattering. Reproduced with permission from Ref. [223]. Copyright 1981 American Chemical Society. (See Ref. [223] for full details.) Note the pattern a is actually located as o in the figure this was an error on the original.
The linewidth-temperature relation of the polyethylene oxide samples are given in Fig. 5. Despite the large differences in molecular weight, these samples have about the same linewidth, 300-350 Hz, in the crystalline state at 25°C. They all also possess a spherulitic type of morphology. The influence on the linewidth of the different types of supermolecular structures... [Pg.185]

As has been emphasized previously (IJ), the level of crystallinity is not the major determinant of the linewidth in the semicrystalline state. Rather the supermolecular structure or morphology is a major factor in governing the magnitude of the linewidth. Structural factors and crystallization conditions under which low density (branched) polyethylene forms... [Pg.199]

Nowadays attention is turned also to the supermolecular level, that is, to the morphologic aspects, to the nature of interfaces, to the formation of new phases, or of particular aggregates (liquid crystals, gels, etc.). Interest has also been directed to the study of chain mobility for its influence on frictional properties of polymers. In recent years there have been many successful approaches to a microscopic theory (in contrast to a phenomenological approach) of the physi-comechanical behavior of macromolecular materials. [Pg.93]

Mesophases of supermolecular structure do not need a rigid mesogen in the constituent molecules. For many of these materials the cause of the liquid crystalline structure is an amphiphilic structure of the molecules. Different parts of the molecules are incompatible relative to each other and are kept in proximity only because of being linked by covalent chemical bonds. Some typical examples are certain block copolymers50 , soap micelles 51 and lipids52. The overall morphology of these substances is distinctly that of a mesophase, the constituent molecules may have, however, only little or no orientational order. The mesophase order is that of a molecular superstructure. [Pg.18]

Morphological or supermolecular structure is the most easily changed property of cellulosic fibers. Interactions of selected monomer solutions with fibers can yield grafted products... [Pg.28]

In the last two decades the value of microhardness measurement as a technique capable of detecting a variety of morphological and textural changes in crystalline polymers has been amply emphasized leading to an extensive research programme in several laboratories. This is because microindentation hardness is based on plastic straining and, consequently, is directly correlated to molecular and supermolecular... [Pg.15]


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See also in sourсe #XX -- [ Pg.274 , Pg.275 , Pg.276 , Pg.277 , Pg.278 , Pg.279 , Pg.280 , Pg.281 , Pg.282 , Pg.283 , Pg.284 , Pg.285 ]




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