Polymer blends, defined

When the iateraction energy density is positive, equation 5 defines a critical temperature of the UCST type (Fig. la) that is a function of component molecular weights. The LCST-type phase diagram, quite common for polymer blends, is not predicted by this simple theory unless B is... 

The all-important difference between the friction properties of elastomers and hard solids is its strong dependence on temperature and speed, demonstrating that these materials are not only elastic, but also have a strong viscous component. Both these aspects are important to achieve a high friction capability. The most obvious effect is that temperature and speed are related through the so-called WLF transformation. For simple systems with a well-defined glass transition temperature the transform is obeyed very accurately. Even for complex polymer blends the transform dominates the behavior deviations are quite small. 

Other combinations of PTs in a blend, 418 412 422 PMMA (PMMA is poly(methyl methacrylate) (10 4 1 1)) produced EL emission of the ITO/polymer blend/PBD/Ca/Al device at 20 V, very close to the equienergy white point as defined by the CIE, while providing a relatively high T 1 = 0.4—0.6% (at 20 V) (Figure 2.31) [515], PMMA was used in this case to... 

Amphiphile-oil-water system, temperature of, 16 424-426 Amphiphiles, 16 420 Amphiphile strength, 6 424 Amphiphilic chemicals, 17 56 Amphiphilic copolymers, 20 482 behavior of, 20 483 well-defined, 20 485-490 Amphiphilic molecules, 15 99-101 Amphiphilic plasticizers, 14 480 Amphiphilic polymer blend, 23 720 Amphiphilic polymers statistical, 20 484-490 stimuli-responsive, 20 482-483 Ampholytes, 9 746-747 Amphoteric cyclocopolymers, water-soluble, 23 721 Amphoteric starches, 4 722 Amphoteric (zwitterionic) surfactants, 24 148... 

Interaction parameters for polymer blends, 20 322 in surfactant adsorption, 24 138 Interaortic balloon pump, 3 746 Intercalated disks, myocardium, 5 79 Intercalate hybrid materials, 13 546-548 Intercalation adducts, 13 536-537 Intercalation compounds, 12 777 Intercritical annealing, 23 298 Interdiffusion, 26 772 Interdigitated electrode capacitance transducer, 14 155 Interesterification, 10 811—813, 831 Interest expense, 9 539 Interface chemistry, in foams, 12 3—19 Interface metallurgy materials, 17 834 Interfaces defined, 24 71... 

Dual Phase Continuity. Dual phase continuity has been shown to be important in numerous polymer blends and IPN s, to achieve special properties. Dual phase continuity is defined as a region of space where two phases maintain some degree of continuity. An example of dual phase continuity is an air filter and the air that flows through it. A Maxwell demon could traverse all space within the air filter phase, as well as within the air phase. 

It is the intent of this doeument to define the terms most commonly encountered in the field of polymer blends and eomposites. The scope has been limited to mixtures in which the eomponents differ in ehemical composition or molar mass or both and in which the continuous phase is polymeric. Many of the materials described by the term multiphase are two-phase systems that may show a multitude of finely dispersed phase domains. Hence, incidental thermodynamic descriptions are mainly limited to binary mixtures, although they can be and, in the scientific literature, have been generalized to multicomponent mixtures. Crystalline polymers and liquid-crystal polymers have been considered in other documents [1,2] and are not discussed here. 

Note 1 The definition and the name of the term have been modified from that which appears in ref. [5] to reflect its broader use in the context of polymer blends. In its simplest form, the %. parameter is defined according to the Flory-Huggins equation for binary mixtures... 

Short block copolymers with well defined number of units in the blocks could be applied as selective absorbents, compatibilizers for polymer blends, components for polymeric membranes, etc. 

Therefore, polyrotaxanes can be simply defined as polymeric materials containing rotaxane units. They are different from conventional linear homopolymers because they always consist of two components, a cyclic species mechanically attached to a linear species. They also differ from polymer blends as the individual species are interlocked together and from block copolymers since the two components are noncovalendy connected. Thus new phase behavior, mechanical properties, molecular shapes and sizes, and different solution properties are expected for polyrotaxanes. Their ultimate properties depend on the chemical compositions of the two components, their interaction and compatibility. This review is designed to summarize the syntheses of these novel polymers and their properties. 

The applications of polymers as solids are usually related to their mechanical properties. These properties often define them as rubbery, glassy or elastomeric materials. Similar to polymer blends, the final properties of polyrotaxanes will de-... 

Macromonomers afford a powerful means of designing a vast variety of well-defined graft copolymers. These species are particularly useful in the field of polymer blends as compatibilizers and/or stabilizers (surfactants). When macromonomer itself is an amphiphilic polymer, then its polymerization in water usually occurs rapidly as a result of organization into micelles. In copolymerizations, important factors for macromonomer reactivity are the thermodynamic repulsion or incompatibility between the macromonomer and the trunk polymer and its partitioning between the continuous phase and the polymer particles [4,5]. 

To discuss the phase stability of polymer blends in more detail one has to specify the free-energy parameter X. This can be done in terms of an equation-of-state theory [8]. Theories that take into account the compressible nature of the pure components as well as that of the mixture are called equation-of-state theories. As basic quantities characterizing the thermodynamic state of a system the reduced temperature (T), volume (V) and pressure (P) are employed and defined by... 

High viscous homogenous mixtures such as polymer blends of well defined components are often difficult to prepare and even more problematic is a production of the relative big sample quantities necessary for some conventional investigation methods. Hence there are demands for "mini method", especially for a method to determine the phase behavior as a function of temperature and pressure. This task is solved to one part by the recently developed "mini extruders" of DSM (1), which enable a very good premixing of small amounts of polymer samples. 

Albertsson and coworkers [240-244] carried out extensive research to develop polymers in which the polymer properties are altered for different applications. The predominant procedure is ring-opening polymerization which provides a way to achieve pure and well defined structures. They have utilized cyclic monomers such as lactones, anhydrides, carbonates, ether-lactones. The work involved the synthesis of monomers not commercially available, studies of polymerization to form homopolymers, random and block copolymers, development of cross-linked polymers and polymer blends, surface modification in some cases, and characterization of the materials formed. The characterization is carried out with respect to the chemical composition and both chemical and physical structures, the degradation behavior in vitro and in vivo, and in some cases the ability to release drug components from microspheres prepared from the polymers. 

Of course, one of the assumptions we made in treating the entropy of mixing was that the lattice cell size is defined by the size of the solvent, so in treating polymer solutions Vr is equal to the molar volume of the solvent. In treating polymer blends you need... 

Regular solutions are mixtures of low molar mass species with Aa = Ab= 1. Polymer solutions are mixtures of macromolecules (Aa = A 1) with the low molar mass solvent defining the lattice (Ab = 1). Polymer blends are mixtures of macromolecules of different chemical species (Aa 1 and Ab > 1). 

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