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Composite schematic

Fig. 8.1 Variation of the activity (logarithmic scale) or galvanic cell voltage as a function of the composition (schematic). The plateaux indicate multi-phase regions in which the activity is fixed according to Gibbs phase rule. Fig. 8.1 Variation of the activity (logarithmic scale) or galvanic cell voltage as a function of the composition (schematic). The plateaux indicate multi-phase regions in which the activity is fixed according to Gibbs phase rule.
The first case, Ef < e, is typical of polymer matrix composites schematic stress-strain curves are given in Figure 15.10. When e < 8, two different modes of failure can take place depending on y. Figure 15.11 gives a schematic representation on the stress-strain curves of the components multiplied by their respective volume fractions as well as the stress-... [Pg.678]

Figure 4.6 Variation in glass transition temperature with copolymer composition (schematic). Figure 4.6 Variation in glass transition temperature with copolymer composition (schematic).
As already discussed, the formation of a nanocrystalline/amorphous (or an nc/nc) composite schematically illustrated in Fig. 4 and its thermal stability require a high immiscibility of the components. This is fulfilled, for example, in systems consisting of a stable transition metal nitride and silicon nitride. A simple estimate shows that in such a system, the immiscibility is assured if the activity of nitrogen is sufficiently high at the given temperature to shift the equilibrium of reaction (10) far to the left hand side [63,73,74]... [Pg.118]

Exhibit 13-47 is a composite schematic sketch of the various containment features covered in the foUowiing... [Pg.341]

Fig. 3.9 Tensile and compressive stresses at interfaces in a monolithic polycrystal and a particulate composite (schematic). After application of tensile load, the distribution of stresses should bring about crack bridging in the case of a, branching in the case of a > Ug—, respectively... Fig. 3.9 Tensile and compressive stresses at interfaces in a monolithic polycrystal and a particulate composite (schematic). After application of tensile load, the distribution of stresses should bring about crack bridging in the case of a, branching in the case of a > Ug—, respectively...
Figure 3 shows such formulation-composition schematic maps, which resemble those found experimentally. In these maps, the formulation is indicated in terms of HLD. The composition is expressed as water content in the water-oil mixture, which is essentially the water fraction in the system because the surfactant concentration is low in most practical cases. It is worth noting that because temperature is a formulation variable, formulation-composition maps and temperature-composition maps can be interpreted analogously. This is particularly important for systems containing nonionic surfactants. [Pg.507]

Shorthand Notation for Electrochemical Cells Although Figure 11.5 provides a useful picture of an electrochemical cell, it does not provide a convenient representation. A more useful representation is a shorthand, or schematic, notation that uses symbols to indicate the different phases present in the electrochemical cell, as well as the composition of each phase. A vertical slash ( ) indicates a phase boundary where a potential develops, and a comma (,) separates species in the same phase, or two phases where no potential develops. Shorthand cell notations begin with the anode and continue to the cathode. The electrochemical cell in Figure 11.5, for example, is described in shorthand notation as... [Pg.467]

Figure 8.2 Schematic illustrations of AGm versus X2 showing how jUj -may be determined by the tangent drawn at any point, (a) The polymer-solvent system forms a single solution at all compositions, (b) Compositions between the two minima separate into equilibrium phases P and Q. Figure 8.2 Schematic illustrations of AGm versus X2 showing how jUj -may be determined by the tangent drawn at any point, (a) The polymer-solvent system forms a single solution at all compositions, (b) Compositions between the two minima separate into equilibrium phases P and Q.
Figure 8.2b is a schematic representation of versus X2 for a system which shows a miscibility gap. Any attempt to prepare a mixture between P and Q in composition will result in separation into the two phases P and Q at equilibrium. [Pg.532]

Insulation Boa.rd. The panel products known as insulation board were the earliest commodity products made from fibers or particles in the composite panel area. These are fiber-base products with a density less than 500 kg/m. Early U.S. patents were obtained in 1915 and production began soon thereafter. The initial production used wood fiber as a raw material, but later products were made of recycled paper, bagasse (sugar cane residue), and straw. Schematics of the two major processes still ia use are shown ia Figure 4. [Pg.385]

Two processes may be used in the manufacture of combustible cases the original post-impregnation process and the more recently and more widely employed beater additive process. The processes differ primarily in the point at which the required resin is added to the composition. A schematic of the beater additive process is shown in Figure 11. [Pg.52]

A more effective carrier confinement is offered by a double heterostmcture in which a thin layer of a low band gap material (the active layer) is sandwiched between larger band gap layers. The physical junction between two materials of different band gaps, and chemical compositions, is called a heterointerface. A schematic representation of the band diagram of such a stmcture is shown in Figure 4. Electrons injected under forward bias across the p—N junction into the lower band gap material encounter a potential barrier, AE at thep—P junction which inhibits their motion away from the junction. The holes see a potential barrier of AE at the N—p heterointerface which prevents their injection into the N region. The result is that the injected minority... [Pg.128]

Interfdci l Composite Membra.nes, A method of making asymmetric membranes involving interfacial polymerization was developed in the 1960s. This technique was used to produce reverse osmosis membranes with dramatically improved salt rejections and water fluxes compared to those prepared by the Loeb-Sourirajan process (28). In the interfacial polymerization method, an aqueous solution of a reactive prepolymer, such as polyamine, is first deposited in the pores of a microporous support membrane, typically a polysulfone ultrafUtration membrane. The amine-loaded support is then immersed in a water-immiscible solvent solution containing a reactant, for example, a diacid chloride in hexane. The amine and acid chloride then react at the interface of the two solutions to form a densely cross-linked, extremely thin membrane layer. This preparation method is shown schematically in Figure 15. The first membrane made was based on polyethylenimine cross-linked with toluene-2,4-diisocyanate (28). The process was later refined at FilmTec Corporation (29,30) and at UOP (31) in the United States, and at Nitto (32) in Japan. [Pg.68]

Fig. 7. Schematic of a self-contained plasma processing unit designed to continuously plasma-treat and impregnate with resin, reinforcing fibers for enhanced composite strength. The unit can also be used to plasma-treat wires to be coated or treated for improved adhesion. Throughput speeds of over... Fig. 7. Schematic of a self-contained plasma processing unit designed to continuously plasma-treat and impregnate with resin, reinforcing fibers for enhanced composite strength. The unit can also be used to plasma-treat wires to be coated or treated for improved adhesion. Throughput speeds of over...
Fig. 12. A spinal-wound leveise osmosis membrane element (a) schematic depiction (b) cross section of a spinal-wound thin-film composite RO Filmtec... Fig. 12. A spinal-wound leveise osmosis membrane element (a) schematic depiction (b) cross section of a spinal-wound thin-film composite RO Filmtec...
Fig. 1. Schematic representation of a battery system also known as an electrochemical transducer where the anode, also known as electron state 1, may be comprised of lithium, magnesium, zinc, cadmium, lead, or hydrogen, and the cathode, or electron state 11, depending on the composition of the anode, may be lead dioxide, manganese dioxide, nickel oxide, iron disulfide, oxygen, silver oxide, or iodine. Fig. 1. Schematic representation of a battery system also known as an electrochemical transducer where the anode, also known as electron state 1, may be comprised of lithium, magnesium, zinc, cadmium, lead, or hydrogen, and the cathode, or electron state 11, depending on the composition of the anode, may be lead dioxide, manganese dioxide, nickel oxide, iron disulfide, oxygen, silver oxide, or iodine.
More than 95% of current carbon fiber production for advanced composite appHcations is based on the thermal conversion of polyacrylonitrile (PAN) or pitch precursors to carbon or graphite fibers. Generally, the conversion of PAN or pitch precursor to carbon fiber involves similar process steps fiber formation, ie, spinning, stabilization to thermoset the fiber, carbonization—graphitization, surface treatment, and sizing. Schematic process flow diagrams are shown in Eigure 4. However, specific process details differ. [Pg.2]

A few industrial catalysts have simple compositions, but the typical catalyst is a complex composite made up of several components, illustrated schematically in Figure 9 by a catalyst for ethylene oxidation. Often it consists largely of a porous support or carrier, with the catalyticaHy active components dispersed on the support surface. For example, petroleum refining catalysts used for reforming of naphtha have about 1 wt% Pt and Re on the surface of a transition alumina such as y-Al203 that has a surface area of several hundred square meters per gram. The expensive metal is dispersed as minute particles or clusters so that a large fraction of the atoms are exposed at the surface and accessible to reactants (see Catalysts, supported). [Pg.170]

Toughening for whisker-reinforced composites has been shown to arise from two separate mechanisms frictional bridging of intact whiskers, and pullout of fractured whiskers, both of which are crack-wake phenomena. These bridging processes are shown schematically in Figure 13. The mechanics of whisker bridging have been addressed (52). The appHed stress intensity factor is given by ... [Pg.55]

Thin-film epitaxy by OMCVD is generally more flexible, faster, lower in cost, and more suited for industrial production than MBE. An OMCVD system usually consists of two principal components, a gas manifold for blending the gas composition, and a graphite substrate holder which is usually inductively heated. A schematic diagram of an OMCVD system is shown in Figure 5. [Pg.118]

Fig. 4. Schematic of an ultrahigh vacuum molecular beam epitaxy (MBE) growth chamber, showing the source ovens from which the Group 111—V elements are evaporated the shutters corresponding to the required elements, such as that ia front of Source 1, which control the composition of the grown layer an electron gun which produces a beam for reflection high energy electron diffraction (rheed) and monitors the crystal stmcture of the growing layer and the substrate holder which rotates to provide more uniformity ia the deposited film. After Ref. 14, see text. Fig. 4. Schematic of an ultrahigh vacuum molecular beam epitaxy (MBE) growth chamber, showing the source ovens from which the Group 111—V elements are evaporated the shutters corresponding to the required elements, such as that ia front of Source 1, which control the composition of the grown layer an electron gun which produces a beam for reflection high energy electron diffraction (rheed) and monitors the crystal stmcture of the growing layer and the substrate holder which rotates to provide more uniformity ia the deposited film. After Ref. 14, see text.

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