Rheology thermodynamics

Design formulas for plastics engineers , Natti S. Rao Hanser Gardner Pubis (1991) ISBN 1569900841. The formulas in this book are classified for specific areas, including rheology, thermodynamic properties, heat transfer, plastic and part type. 

This somewhat critical situation may be resolved by the determination of specific and general physical and chemical regularities governing the formation and behavior of polymeric foams, which requires the use of a wide range of ideas and techniques developed in other sciences physical and colloidal chemistry, physicochemical mechanics, rheology, thermodynamics, physics of polymers, physics and mechanics of non-continuous media, physics of surface and transfer phenomena, chemical physics of oxidation and degradation processes, etc. 

Wagner, M.H. (1976) Blown film extrusion as rheological-thermodynamic process. Rheol. Acta., 15, 40-51. 

Neither the thermodynamic nor the rheological description of surface mobility has been very useful in the case of chemisorbed films. From the experimental point of view, the first is complicated by the many factors that can affect adsorption entropies and the latter by the lack of any methodology. 

Viscoelastic polymers essentially dominate the multi-billion dollar adhesives market, therefore an understanding of their adhesion behavior is very important. Adhesion of these materials involves quite a few chemical and physical phenomena. As with elastic materials, the chemical interactions and affinities in the interface provide the fundamental link for transmission of stress between the contacting bodies. This intrinsic resistance to detachment is usually augmented several folds by dissipation processes available to the viscoelastic media. The dissipation processes can have either a thermodynamic origin such as recoiling of the stretched polymeric chains upon detachment, or a dynamic and rate-sensitive nature as in chain pull-out, chain disentanglement and deformation-related rheological losses in the bulk of materials and in the vicinity of interface. 

Thermodynamics of Irreversible Processes Applications to Diffusion and Rheology... 

A large number of studies have been conducted to elucidate the rheology and thermodynamics of binary... 

Viscoelasticity of metal This subject provides an introduction on the viscoelasticity of metals that has no bearing or relationship with viscoelastic properties of plastic materials. The aim is to have the reader recognize that the complex thermodynamic foundations of the theory of viscoplasticity exist with metals. There have been developments in the thermodynamic approach to combined treatment of rheologic and plastic phenomena and to construct a thermodynamic theory non-linear viscoplastic material that may be used to describe the behavior of metals under dynamic loads. 

There are three different approaches to a thermodynamic theory of continuum that can be distinguished. These approaches differ from each other by the fundamental postulates on which the theory is based. All of them are characterized by the same fundamental requirement that the results should be obtained without having recourse to statistical or kinetic theories. None of these approaches is concerned with the atomic structure of the material. Therefore, they represent a pure phenomenological approach. The principal postulates of the first approach, usually called the classical thermodynamics of irreversible processes, are documented. The principle of local state is assumed to be valid. The equation of entropy balance is assumed to involve a term expressing the entropy production which can be represented as a sum of products of fluxes and forces. This term is zero for a state of equilibrium and positive for an irreversible process. The fluxes are function of forces, not necessarily linear. However, the reciprocity relations concern only coefficients of the linear terms of the series expansions. Using methods of this approach, a thermodynamic description of elastic, rheologic and plastic materials was obtained. 

The ultimate goal is to bring together knowledge of solution thermodynamics, rheology and polymerization kinetics so that the latter, which is well described at low conversion (12,13), may be better described in a continuous manner to complete conversion. 

Advanced adhesives are composite liquids that can be used, for example, to join aircraft parts, thus avoiding the use of some 30,000 rivets that are heavy, are labor-intensive to install, and pose quality-control problems. Adhesives research has not involved many chemical engineers, but the generic problems include surface science, polymer rheology and thermodynamics, and molecular modeling of materials... 

In view of the above developments, it is now possible to formulate theories of the complex phase behavior and critical phenomena that one observes in stractured continua. Furthermore, there is currently little data on the transport properties, rheological characteristics, and thermomechaiucal properties of such materials, but the thermodynamics and dynamics of these materials subject to long-range interparticle interactions (e.g., disjoiiung pressure effects, phase separation, and viscoelastic behavior) can now be approached systematically. Such studies will lead to sigiuficant intellectual and practical advances. 

PP is probably the most thoroughly investigated system in the nanocomposite field next to nylon [127-132]. In most of the cases isotactic/syndiotactic-PP-based nanocomposites have been prepared with various clays using maleic anhydride as the compatibilizer. Sometimes maleic anhydride-grafted PP has also been used [127]. Nanocomposites have shown dramatic improvement over the pristine polymer in mechanical, rheological, thermal, and barrier properties [132-138]. Crystallization [139,140], thermodynamic behavior, and kinetic study [141] have also been done. 

Kammer, H. W., Kressler, H. and Kummerioewe, C Phase Behavior of Polymer Blends - Effects of Thermodynamics and Rheology. Vol. 106, pp, 31-86. 

In this chapter we have discussed the thermodynamic formation of blends and their behavior. Both miscible and immiscible blends can be created to provide a balance of physical properties based on the individual polymers. The appropriate choice of the blend components can create polymeric materials with excellent properties. On the down side, their manufacture can be rather tricky due to rheological and thermodynamic considerations. In addition, they can experience issues with stability after manufacture due to phase segregation and phase growth. Despite these complications, they offer polymer engineers and material scientists a broad array of materials to meet many demanding application needs. 

Utracki, L.A. Polymer Alloys and Blends Thermodynamics and Rheology. (1990)Hanser Publishers, New York. 

The dynamic behavior of fluid interfaces is usually described in terms of surface rheology. Monolayer-covered interfaces may display dramatically different rheological behavior from that of the clean liquid interface. These time-dependent properties vary with the extent of intermolecular association within the monolayer at a given thermodynamic state, which in turn may be related directly to molecular size, shape, and charge (Manheimer and Schechter, 1970). Two of these time-dependent rheological properties are discussed here surface shear viscosity and dynamic surface tension. 

The implications for films cast from mixtures of enantiomers is that diagrams similar to those obtained for phase changes (i.e., melting point, etc.) versus composition for the bulk surfactant may be obtained if a film property is plotted as a function of composition. In the case of enantiomeric mixtures, these monolayer properties should be symmetric about the racemic mixture, and may help to determine whether the associations in the racemic film are homochiral, heterochiral, or ideal. Monolayers cast from non-enantiomeric chiral surfactant mixtures normally will not exhibit this feature. In addition, a systematic study of binary films cast from a mixture of chiral and achiral surfactants may help to determine the limits for chiral discrimination in monolayers doped with an achiral diluent. However, to our knowledge, there has never been any other systematic investigation of the thermodynamic, rheological and mixing properties of chiral monolayers than those reported below from this laboratory. 

The model includes a dynamic thermodynamic sea ice model. The dynamics of sea ice are formulated using viscous-plastic rheology [Hibler (1979)]. The thermodynamics relate changes in sea ice thickness to a balance of radiant, turbulent, and oceanic heat fluxes. The effect of snow accumulation on sea ice is included, along... 

I. Gutzow and J. Schmelzer, The Vitreous State. Thermodynamics, Structure, Rheology and... 

Now, in rheological terminology, our compressibility JT, is our bulk compliance and the bulk elastic modulus K = 1 /Jr- This is not a surprise of course, as the difference in the heat capacities is the rate of change of the pV term with temperature, and pressure is the bulk stress and the relative volume change, the bulk strain. Immediately we can see the relationship between the thermodynamic and rheological expressions. If, for example, we use the equation of state for a perfect gas, substituting pV = RTinto a = /V(dV/dT)p yields a = R/pV = /Tand so for our perfect gas ... 

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