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Highest amorphous materials

Amplitudes of the structure factors are sampled by D(u)sinx(u) when they are transferred to the image. The most significant effect of the lens to the amplitudes is caused by the sinx(u) part, which oscillates with u. Reflections in the resolution regions where sinx(u) 1 are maximally transferred by the lens, while those at resolutions where sinx(u) 0 are not transferred at all. This can be seen in the Fourier transform of HREM images from amorphous materials (Fig. 6), where the highest amplitudes (brightest areas) correspond to sinx(u) 1, while the lowest amplitudes (darkest areas) correspond to sinx(u) 0. If there is no astigmatism in the objective lens, a... [Pg.287]

The zeolite products with the highest XRD intensities and with the lowest amorphous material impurities were used as the quantitative standards for both Na-ZSM-5 and mordenite. The degree of crystallization was estimated by comparing the sum of the respective XRD peak areas (around 20 = 20-30°) with those of the standard. [Pg.245]

The glass transition temperature, T, is the temperature at which an amorphous material changes from a brittle glassy state to a rubbery state. Poly(methyl methacrylate) has the highest glass transition temperature (105°C) and poly(2-ethylhexyl-acrylate) the lowest (-55°C). Other predominantly acrylic polymers and copolymers lie between the two (Edward, 1968). [Pg.103]

The relative proportions of amorphous, exinous and vitrinous plus fusinous kerogen material in the few samples examined to date are shown in Figure 7. Whitby Formation kerogens from the Collingwood area are highest in amorphous material and so one... [Pg.138]

Electron Microscopic Results. The fundamental deformation step is the formation of crazes at the rubber particles (Figure 4). The crazes start directly at the interface between rubber particles and matrix in the equatorial zones around the particles, that is, in the zones of highest stress concentration. The structure of the amorphous material is transformed by local plastic defor-... [Pg.262]

Monolithic zirconia networks can also be formed using a similar procedure giving porous 2xQ>2 structures [9]. As the titania and zirconia precursors are miscible, binary inorganic networks of various Ti Zr ratios could be produced [9]. The crystallinity and photocatalytic properties of the mixed material were studied X-ray amorphous materials were produced for Ti Zr ratios of 2 8 to 7 3, and the binary material containing 10% zirconia (the presence of which inhibited crystal transformation to the rutile phase) showed the highest photocatalytic activity for the photodecomposition of sahcylic acid and 2-chlorophenol [9]. [Pg.97]

It cannot be said that one particular strategy - order versus disorder - is better than the other, and the choice will depend on the desired application. There are a number of potential advantages for crystalline MOPs. Structural uniformity makes it possible to design materials with very narrow pore size distributions and thus, conceivably, gain some of the advantages associated with zeolites [1] - for example, molecular specificity in catalysis. Crystalline MOPs can also be characterized structurally at the molecular level by X-ray diffraction [14,15, 20] in a manner that is not possible for amorphous materials. At the time of writing, the highest apparent BET surface areas reported for MOPs (up to 4,210 m g ) were found for ordered, crystalhne COFs [20]. [Pg.8]

LiN(S02CF3)2. Not only was the electrolyte film of 55 wt % MEEP 45 wt % PEO-[LiN(S02CF3)2]o.i3 dimensionally stable, but it also exhibited a conductivity of 6.7 x 10 Scm" at 25°C, among the highest reported to date for a dimensionally stable conventional polymer electrolyte. The log conductivity versus 1/T plot for this electrolyte given in Figure 3.4 has a profile expected for an amorphous material showing the VTF behaviour. [Pg.89]


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Amorphous materials

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