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Melt processing, description

The review of Duvall and Graham [77D01], the paper of Brown and Shaner [84B02], and the book of Young [91Y02] provide thermodynamic descriptions of the melt process. [Pg.49]

In the following, a description of the melting processes of liquid crystals will be given, and then the general structures of the nematic, smectic A and smectic C achiral and chiral phases that are involved in TGB phenomena will be discussed. When mesophases are formed by molecules (such as 1) that have asymmetric or dissymmetric structures, a reduction in the environmental space symmetry occurs, which in some cases can induce the creation of helical... [Pg.84]

General Description Fluorinated ethylene propylene (FEP), a melt-processable fluorocarbon, is a copolymer of tetrafluoroethylene (TFE) and hexafluo-ropropylene. Fluorinated ethylene propylene and TFE yield similar properties, with the exception ofTFE s lowermelt viscosity.fl 1 DuPont s high-performance material Teflon FEP film is a transparent, thermoplastic film.P ... [Pg.17]

Rauwendaal [259] presented the first theoretical model of DSM that allows analytical description of the melting process. In the following, this theory will be described in detail. Predictions from the DSM theory will be compared to the CSM theory. [Pg.334]

From this description of melting it is clear that the thickness of the melt film is an important parameter in the melting process. A thin melt film is important in maintaining high melting efficiency. With a thin melt film, there is high viscous... [Pg.3010]

The cationic copolymerization of trioxane with ethylene oxide, 1,3-dioxolane, and suchlike is initiated either with strong protonic acids or Lewis acids, for example BF3. Molecular weight is controlled by the catalyst concentration and monomer purity, and also by chain transfer agents such as methylal [248], which may lead to more stable end groups. Most processes are run below the melting temperature of the polymer (164-167°C) in precipitating agents or in bulk, and are carried out in kneaders or double-screw reactors [249, 250], but there are also some descriptions of melt processes [251]. [Pg.356]

The brief description of the commercially important fluoropolymers indicates the techniques by which they can be fabricated. Generally, the processing method is dependent on the rheology of the fiuoropoly-mer in question. Table 3.6 summarizes the structure-rheology-fabrication technique characteristics of various copolymers. Melt viscosity values represent a wide range of shear rate for melt processible polymers in Table 3.6. Volume One focuses on fluoropolymers which are processed by non-melt methods.The present volume is devoted to the melt processible fluoropolymers. [Pg.27]

The melting enthalpy of a polymer crystal Aff°m is generally determined by combining differential scanning calorimetry (DSC) with an independent method (eg, dilatometry). By measuring the values of AH°,n and simultaneously the density p of a pol3uner in various states, one determines A/f °m by linear extrapolation of the Aff°m (p) to the crystal density Pc. The detailed description of the melting processes in polymers may be found in the excellent book written by Wunderlich (13). [Pg.1231]

The quasiharmonic approximation studied in Sects.5.2,3 gives reasonable results for the thermodynamic properties of crystals in which the anhar-monicity is weak and the force constants are renormalized by thermal expansion only. In crystals with very strong enharmonic interactions, however, this approximation breaks down. Examples are the vibrations in rare-gas solids, in particular solid helium, soft modes in ferro-electric phase transitions and melting processes. For these cases a method has been developed, the self-consistent harmonic approximation (SCHA), which allows a qualitative description of the effects of strong anharmonicity. [Pg.175]

The second transition to be discussed is a kind of lower dimensional melting. The description of the melting of a solid as a first-order phase transition is a consequence of the discontinuous change in bulk quantities at the transition point. However, every crystal is finite, and bounded by its own surface area where the process of melting may actually be initiated If there were a layer of liquid at the surface, at temperatures below the bulk melting fransition, then there is little need to activate the melting proc-... [Pg.43]

The experiments carried out for this work allow for the first time a look at the melting process of the processing of plastic polymers with this short extruder. All of the experiments were carried out with a standard polymer (PS). The tests showed an influence of the parameters throughput, screw speed and die pressure on the melting process. The melting takes place at a compacted solid bed, making a modified Tadmor model usable for a theoretical description. However, since the results are based on experiments with one material only such a model has not been created, yet. [Pg.1659]

Polymers owe much of their attractiveness to their ease of processing. In many important teclmiques, such as injection moulding, fibre spinning and film fonnation, polymers are processed in the melt, so that their flow behaviour is of paramount importance. Because of the viscoelastic properties of polymers, their flow behaviour is much more complex than that of Newtonian liquids for which the viscosity is the only essential parameter. In polymer melts, the recoverable shear compliance, which relates to the elastic forces, is used in addition to the viscosity in the description of flow [48]. [Pg.2534]


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See also in sourсe #XX -- [ Pg.179 ]




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