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Polymer mixing blends

DMPPO and polystyrene form compatible blends. The two components are miscible in all proportions (59). Reported dynamic—mechanical results that indicate the presence of two phases in some blends apparendy are caused by incomplete mixing (60). Transition behavior of thoroughly mixed blends indicates that the polymers are truly compatible on a segmental level (61). CompatibiUty may be attributed to a %— % interaction between the aromatic rings of the two polymers sufficient to produce a negative heat of mixing. However, the forces are very small, ie, = ca40 J/mol (9.6 cal/g), and any... [Pg.330]

The science and technology of polymer blends has been extensively studied and reviewed [4-7]. The thermodynamics of polymer mixing of polymer 1 and 2 can be described by the Flory-Huggins [8-9] equation,... [Pg.299]

Compositions of the ABS type may be mixed with other polymers. Suitable blend partners can be selected from poly(carbonate)s (PC)s, poly(ester)s, poly(ester carbonate)s and poly(amide)s (PA)s. Some especially preferred types, of these compounds and an overview of how to produced these types have been described (16). [Pg.221]

Polymers Mixed by Milling. The effect of EVA concentration in the blends on gas permeation and light transmission through the film was studied. The permeability and the diffusion coefficients at 50 °C for the penetrants helium, argon, and carbon dioxide are shown in Figures 1, 2,... [Pg.123]

VVThen two chemically different polymers are mixed, the usual result is a two-phase polyblend. This is true also when the compositional moities are part of the same polymer chain such as, for instance, in a block polymer. The criterion for the formation of a single phase is a negative free energy of mixing, but this condition is rarely realized because the small entropy of mixing is usually insufficient to overcome the positive enthalpy of mixing. The incompatibility of polymers in blends has important effects on their physical properties, which may be desirable or not, depending on the contemplated application. [Pg.200]

The supramolecular structure of block co-polymers allows the design of useful materials properties such as polarity leading to potential applications as second-order nonlinear optical materials, as well as piezo-, pyro-, and ferroelectricity. It is possible to prepare polar superlattices by mixing (blending) a 1 1 ratio of a polystyrene)-6-poly(butadiene)-6-poly-(tert-butyl methacrylate) triblock copolymer (SBT) and a poly (styrene)-Apoly (tert-butyl methacrylate) diblock copolymer (st). The result is a polar, lamellar material with a domain spacing of about 60 nm, Figure 14.10. [Pg.906]

Fig. 11.33 Dispersed PS 685 streaks of ligaments and droplets in the equiviscous Blend 2. PS is flowing/deforming in an affine fashion in the expected stretching and folding pattern. Experiments were conducted at 180°C and 120rpm. [Reprinted with permission from Proceedings of the Tenth Semiannual Meeting of the Polymer Mixing Study, Polymer Processing Institute, Hoboken, NJ (1995).]... Fig. 11.33 Dispersed PS 685 streaks of ligaments and droplets in the equiviscous Blend 2. PS is flowing/deforming in an affine fashion in the expected stretching and folding pattern. Experiments were conducted at 180°C and 120rpm. [Reprinted with permission from Proceedings of the Tenth Semiannual Meeting of the Polymer Mixing Study, Polymer Processing Institute, Hoboken, NJ (1995).]...
Fig. 11.40 Extmdate of Blend 1 emerging from the SSMEE with a 3.5 L/D Maddock mixer operating at 140°C and 90rpm. [Reprinted hy permission from the Proceedings of the Fourth Semiannual Meeting of the Polymer Mixing Study, Polymer Processing Institute, Hohoken, NJ (1992).]... Fig. 11.40 Extmdate of Blend 1 emerging from the SSMEE with a 3.5 L/D Maddock mixer operating at 140°C and 90rpm. [Reprinted hy permission from the Proceedings of the Fourth Semiannual Meeting of the Polymer Mixing Study, Polymer Processing Institute, Hohoken, NJ (1992).]...
Fig. 11.45 Blend 3a morphology developed in the SSMEE at 180°C and 80rpm. SEM image of the carcass. [Reprinted by permission from the Proceedings of the Sixth Semi-annual Meeting, Polymer Mixing Study, Polymer Processing Institute, Hoboken, NJ (1993).]... Fig. 11.45 Blend 3a morphology developed in the SSMEE at 180°C and 80rpm. SEM image of the carcass. [Reprinted by permission from the Proceedings of the Sixth Semi-annual Meeting, Polymer Mixing Study, Polymer Processing Institute, Hoboken, NJ (1993).]...
Several organics, e.g. pristine poly(3-octylthiophene), polyfluorene, bifunctional spiro compounds and polyphenyleneethynylene derivative, have been used for fabricating photOFETs. Responsivity as high as 0.5-1 A/W has been achieved in some of these transistors. We have already discussed the bulk heterojunction concept in Chapter 5. The bulk heterojunctions are fabricated using acceptor materials with high electron affinity (such as C<5o or soluble derivatives of C6o) mixed with conjugated polymers as electron donors. PhotOFETs based on conjugated polymer/fullerene blends are expected to show... [Pg.151]


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