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Immiscible blends morphology

In addition to changes and variation in morphology, immiscible blends show additional, more complex changes due to different chemical properties of the two-component elastomer. This difference in the chemical structure manifests as three distinct but interrelated properties. First, the dissimilar elastomers differ in the retention of the fillers (e.g., carbon black) and plasticizers (e.g.. [Pg.548]

Why does the minor component in an immiscible blend prefer to form spherical morphologies in the absence of applied stresses How do the less stable shapes of rods or platelets form ... [Pg.211]

The effect of blending LDPE with EVA or a styrene-isoprene block copolymer was investigated (178). The properties (thermal expansion coefficient. Young s modulus, thermal conductivity) of the foamed blends usually lie between the limits of the foamed constituents, although the relationship between property and blend content is not always linear. The reasons must he in the microstructure most polymer pairs are immiscible, but some such as PS/polyphenylene oxide (PPO) are miscible. Eor the immiscible blends, the majority phase tends to be continuous, but the form of the minor phase can vary. Blends of EVA and metallocene catalysed ethylene-octene copolymer have different morphologies depending on the EVA content (5). With 25% EVA, the EVA phase appears as fine spherical inclusions in the LDPE matrix. The results of these experiments on polymer films will apply to foams made from the same polymers. [Pg.4]

Recently, a new concept in the preparation of TPVs has been introduced, based on the reaction-induced phase separation (RIPS) of miscible blends of a semicrystalline thermoplastic in combination with an elastomer, with the potential for obtaining submicrometer rubber dispersions. This RIPS can be applied to a variety of miscible blends, in which the elastomer precursor phase was selectively crosslinked to induce phase separation. Plausible schematic representation of the morphological evolution of dynamic vulcanization of immiscible and miscible blends is shown in Fig. 9. For immiscible blends, dynamic vulcanization leads to a decrease in the size... [Pg.234]

In this example of model reactive polymer processing of two immiscible blend components, as with Example 11.1, we have three characteristic process times tD,, and the time to increase the interfacial area, all affecting the RME results. This example of stacked miscible layers is appealing because of the simple and direct connection between the interfacial layer and the stress required to stretch the multilayer sample. In Example 11.1 the initially segregated samples do create with time at 270°C an interfacial layer around each PET particulate, but the torsional dynamic steady deformation torques can not be simply related to the thickness of the interfacial layer, <5/. However, the initially segregated morphology of the powder samples of Example 11.1 are more representative of real particulate blend reaction systems. [Pg.632]

Fig. 11.17 The melting mechanism of immiscible blends, showing in cartoon form the evolution of blend morphology during and following melting in twin rotor devices. [Reprinted by permission from C. E. Scott and C. W. Macosko, Morphology Development During the Initial Stages of Polymer-polymer Blending, Polymer, 36, 461-470, (1995).]... Fig. 11.17 The melting mechanism of immiscible blends, showing in cartoon form the evolution of blend morphology during and following melting in twin rotor devices. [Reprinted by permission from C. E. Scott and C. W. Macosko, Morphology Development During the Initial Stages of Polymer-polymer Blending, Polymer, 36, 461-470, (1995).]...
The use of copolymers as surfactants is widespread in macromolecular chemistry in order to compatibilize immiscible blends. These additives are sometimes named surfactants , interfacial agents or more usually compatibi-lizers . Their effect on improving different properties is observed interfacial tension and domain size decrease, while there is an increase in adhesion between the two phases and a post-mixing morphology stabilization (coalescence prevention). The aim of the addition of such copolymers is to obtain thermodynamically stable blends, but the influence of kinetic parameters has to be kept in mind as long as they have to be mastered to reach the equilibrium. Introducing a copolymer can be achieved either by addition of a pre-synthesized copolymer or by in-situ surfactant synthesis via a fitted re-... [Pg.118]

Blend morphology commonly depends on the weight fraction and viscoelastic properties of each component, the interfacial tension between components, the shape and sizes of the discontinuous phase, and the fabrication conditions and setup. Most rheological experiments applied to homogeneous melts can also be similarly applied to these immiscible blends [55,63,88,89]. The viscoelastic properties arising from these studies should be labeled with a subscript apparent since the equations used to translate rheometer transducer responses to properties incorrectly assume that the material is homogeneous. Nevertheless, these apparent properties are often found to be excellent metrics of fabrication performance. [Pg.295]

Coherently, as expected for immiscible blends, Tg values measured by DSC show very small variations with respect to the pure components while the mechanical properties degrade with respect to neat sPS. In particular, for minimum polyolefin contents <40 wt%, uniaxial tensile tests revealed a decrease in Young s modulus, elongation at break and energy to break. For higher contents, a phase inversion of the morphology occurs and the blend properties approach progressively those of the pure polyolefins. [Pg.447]

Hong et al. [42] studied the effect of SEBS (LMW-SEBS with molecular weight 50000 and HMW-SEBS with molecular weight 175000) on the morphological, mechanical and rheological properties of sPS/EPR immiscible blends (80 20 wt%), melted at 300 °C for 15 min and injection molded. In the binary blend, SEM showed the presence of large domains well separated at the interface. With the compatibilizer, the dispersion of EPR becomes narrow and... [Pg.456]

There are a number of important factors governing the change of the crystallization rate and semicrystalline stracture of a polymer in blend systems. Those include the degree of miscibility of the constituent polymers, their concentration, their glass-transition and melting temperamre, the phase morphology and the interface structure in the case of immiscible blends, etc. [Pg.205]

Immiscible blends most often show a two phase morphology consisting of a continuous matrix... [Pg.274]

The structure and morphology of immiscible blends depends on many factors among which the flow history and the interfacial properties are the most important. At high dilution, and at low flow rates the morphology of polymer blends is controlled by three dimensionless microrheologi-cal parameters (i) the viscosity ratio, where r j is the viscosity of the dispersed liquid and r 2 that of the matrix (ii) the capillarity number, k = d / Vj2, where d... [Pg.296]

To select proper compatibilizer, it is imperative to know whether the copolymer is capable to (i) engender a hne dispersion during blending, (ii) preferentially migrate to the homopolymers interface, (iii) stabilize the morphology against segregation, and (iv) enhance the adhesion between the phases. It is only when all these conditions are satished that the idea of interfacial activity of classical emulsifiers can be applied to copolymers added to immiscible blends. [Pg.329]


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See also in sourсe #XX -- [ Pg.60 ]




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