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Morphology required materials

Some product is sold in slurry which is a convenient form since it eliminates dust, saves energy, and lowers the cost. The industries which are frequent users of such product are paper and paints. Many other applications require material to be in a powder form, therefore the sluny is flocculated, concentrated (filter presses), and dried. Several dryer types are used such as rotary, tray, fluidized bed process or spray. The clay may be pulverized after some of these drying process depending requirements. Figure 2.34 shows the morphology of kaolin. A typical platy structure is clearly displayed on this photograph. [Pg.102]

Plashcizers are also used to adjust morphology dining material formahon. The required degree of crystallinity is achieved due to increased mobihty in the presence of... [Pg.216]

Furthermore, the electrical properties can be adjusted by varying the matrix polymer and the filler distribution. Since the material concept allows for the use of almost any polymer matrix, the required material properties, for instance a high temperature resistance, can be provided by the use of polyphenylene sulfide (PPS) as a matrix polymer. The morphological structure, and thus the measured conductivity over the thickness, depend on the ratio of the melt temperatures and viscosities of both the polymer and metal alloy, whereas the passage conductivity is at a similarly high level of >4x10 S/m. [Pg.48]

Many of the methods described above can be used to prepare nanoparticles if the experimental details are fixed to specific values. The methods are named as top-down methods when bulk materials are first prepared and then are manipulated to the size and morphology required, and bottom-up procedures, when a structure is built atom by atom. [Pg.18]

Several relations have been proposed in literature by giving the volume fraction at which co-continuity can be formed as a fimction of the viscosity ratio. These include the relations proposed by Paul and Barlow [65], Jordhamo et al. [66], Metelkin and Blekht [67], and Utracki [68]. All these relations describe the phase inversion as a function of the viscosity ratio. It has been shown by Willemse et al. that the viscosity ratio alone is not sufficient to predict the phase inversion point in all cases [69]. Parameters such as the interfacial tension, the absolute values of the viscosities rather than their ratio, the phase dimensions, and the mixing conditions can have an important effect on the formation of continuous phase structures. Therefore, Willemse et al. proposed a new empirical model by introducing the dependence of the formation of the continuous morphology on material properties (matrix viscosity, interfacial tension) and processing conditions via the consideration of the shape of the dispersed phase required for achieving phase cocontinuity [69]. [Pg.65]

As with chemical etches, developing optimum conversion coatings requires assessment of the microstructure of the steel. Correlations have been found between the microstructure of the substrate material and the nature of the phosphate films formed. Aloru et al. demonstrated that the type of phosphate crystal formed varies with the orientation of the underlying steel crystal lattice [154]. Fig. 32 illustrates the different phosphate crystal morphologies that formed on two heat-treated surfaces. The fine flake structure formed on the tempered martensite surface promotes adhesion more effectively than the knobby protrusions formed on the cold-rolled steel. [Pg.991]

Commercial thermoplastics are the engineering materials containing two or more compatibilized polymers that are chemically bounded in a way that creates a controlled and stable morphology with a unified thermodynamic profile. In view of multiplicity and contradictory requirements of various properties for most of the applications, almost all the commercial PBAs are made of two or more thermoplastics, elastomeric modifiers along with a series of compatibilizers with modifiers compounded together. A considerable number of blends have been appearing in the market regularly, some of which are listed in Table 9. [Pg.660]

The possibility of controlling ihc morphological and structural order in the solid is therefore a fundamental requirement for the control and reproducibility of the emission properties of a luminescent material within an organic light emitting diode (OLED) device. [Pg.420]

A reactive polymer (RP) is simply a device to alloy different materials by changing their molecular structure inside a compounding machine. True reactive alloying induces an interaction between different phases of an incompatible mixture and assures the stability of the mixture s morphology. The concept is not new. This technology is now capable of producing thousands of new compounds to meet specific design requirements. [Pg.348]

Recent demands for polymeric materials request them to be multifunctional and high performance. Therefore, the research and development of composite materials have become more important because single-polymeric materials can never satisfy such requests. Especially, nanocomposite materials where nanoscale fillers are incorporated with polymeric materials draw much more attention, which accelerates the development of evaluation techniques that have nanometer-scale resolution." To date, transmission electron microscopy (TEM) has been widely used for this purpose, while the technique never catches mechanical information of such materials in general. The realization of much-higher-performance materials requires the evaluation technique that enables us to investigate morphological and mechanical properties at the same time. AFM must be an appropriate candidate because it has almost comparable resolution with TEM. Furthermore, mechanical properties can be readily obtained by AFM due to the fact that the sharp probe tip attached to soft cantilever directly touches the surface of materials in question. Therefore, many of polymer researchers have started to use this novel technique." In this section, we introduce the results using the method described in Section 21.3.3 on CB-reinforced NR. [Pg.597]


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