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Scanning electron microscopy microstructures

A number of techniques have been employed that are capable of giving information about amorphous phases. These include infrared spectroscopy, especially the use of the attenuated total reflection (ATR) or Fourier transform (FT) techniques. They also include electron probe microanalysis, scanning electron microscopy, and nuclear magnetic resonance (NMR) spectroscopy. Nor are wet chemical methods to be neglected for they, too, form part of the armoury of methods that have been used to elucidate the chemistry and microstructure of these materials. [Pg.359]

Structural changes on the whey proteins from the effect of extrusion cooking were examined by scanning electron microscopy and TEM. Changes in the microstructure of WPI (Pig. 5.3) show the transition from... [Pg.182]

The essential step is the efficient grinding and blending of raw materials. The final properties of cement strongly depend on its mineral composition so that raw composition and firing conditions are adjusted, depending on the type of cement to be produced. The microstructure of the steel fiber-cement paste interface was studied by scanning electron microscopy (SEM). The interfacial zone surrounding the fiber was found to be substantially different from the bulk paste further away from the fiber surface. The interfacial zone consisted of... [Pg.220]

Scanning electron microscopy (SEM) is a powerful tool used to study the surface topography of potato chips. Figure 11.5 shows that potato chips lose a considerable quantity of surface oil after they are washed in petroleum ether, which allows clear observation of the cellular microstructure of the surface (Figures 11.5bl, 11.5b2 and 11.5b3) (Pedresehi etal., 2008). [Pg.325]

FIG. 1.13 Spherical and cubic model particles with crystalline or amorphous microstructure (a) spherical zinc sulfide particles (transmission electron microscopy, TEM, see Section 1.6a.2a) x-ray diffraction studies show that the microstructure of these particles is crystalline (b) cubic lead sulfide particles (scanning electron microscopy, SEM, see Section 1.6a.2a) (c) amorphous spherical particles of manganese (II) phosphate (TEM) and (d) crystalline cubic cadmium carbonate particles (SEM). (Reprinted with permission of Matijevic 1993.)... [Pg.24]

A.H. Deutchman and R.J. Partyka (Beam Alloy Corporation observe, "Characterization and classification of thin diamond films depend both on advanced surface-analysis techniques capable of analyzing elemental composition and microstructure (morphology and crystallinity), and on measurement of macroscopic mechanical, electrical, optical and thermal properties. Because diamond films are very thin (I to 2 micrometers or less) and grain and crystal sizes are very small, scanning electron microscopy... [Pg.485]

The phase composition from the surface to the interior of the samples was determined by X-ray diffractometry (XRD) through successive grinding of the surface at 100 pm intervals. The microstructural characterization of the sintered specimens was achieved by scanning electron microscopy (SEM) in backscattered mode. The hardness change from the surface to the interior of the sample was measured by the Vickers indentation method at 19.6 N load. [Pg.162]

Figure 9-6 The scanning electron microscopy (SEM) in the backscattered mode, the energy dispersive X-ray (EDX) spectrum and X-ray distribution maps of a spherical particle from Sudbury soil showing Ni and Fe microstructures in a silicate matrix (from Adamo et al., 1996). Figure 9-6 The scanning electron microscopy (SEM) in the backscattered mode, the energy dispersive X-ray (EDX) spectrum and X-ray distribution maps of a spherical particle from Sudbury soil showing Ni and Fe microstructures in a silicate matrix (from Adamo et al., 1996).
Microstructured films were characterized by scanning electron microscopy (LEO GEMINI DSM 982/Carl Zeiss NTS GmbH, Oberkochen, Germany) at low voltages (0.9-1 keV) in order to avoid sample charging. [Pg.16]

Rayan, A.A., Kalab, M., Ernstrom, C.A. 1980. Microstructure and rheology of process cheese. Scanning Electron Microscopy, III, 635—643. [Pg.437]

As was detailed in this section, TEM can bring numerous pieces of information regarding the polymer/nanotube composite microstructure. However, it has to be recalled that nanofillers such as nanotubes easily agglomerates and their dispersion state has to be characterised from the micron to the nanometre scale. This is one reason, among others, why Scanning Electron Microscopy is another widely used to characterise polymer/nanotube composites. [Pg.67]

PA6 phase of the blends. This approach was further extended to PA6 based ternary and quaternary blends in an attempt to find the applicability of this strategy. Raman spectroscopy and transmission electron microscopy (TEM) have been performed to get more insights into the role of these modifiers in debundling the MWNTs. AC electrical conductivity measurements have been carried out to assess the state of dispersion of MWNTs in the blends. Further, the phase microstructures and the localization of MWNTs in the blends have been investigated using scanning electron microscopy (SEM). [Pg.376]

There are a number of indicators of fatigue damage that have attracted interest in the literature. During the life of a component subjected to fatigue, the material can exhibit changes in modulus, permanent offset strain, shape of the hysteresis loops, and temperature rise of the specimen surface. Direct evidence of matrix crack density can be obtained by surface replication, while a more detailed analysis of microstructural damage requires scanning electron microscopy (SEM). [Pg.202]

Electron microscopy, with its high spatial resolution, plays an important role in the physical characterization of these catalysts. Scanning electron microscopy (SEM) is used to characterize the molecular sieve particle sizes and morphologies as a function of preparation conditions. Transmission electron microscopy (TEM) is used to follow the changes in the microstructure of the iron silicates caused by different growth conditions and subsequent thermal and hydrothermal treatments. [Pg.368]

The phases, microstructure and chemical composition at the sink side of the PEVD system were studied before and after the PEVD process by x-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive x-ray (EDX) spectroscopy, respectively. [Pg.126]


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See also in sourсe #XX -- [ Pg.71 , Pg.203 ]




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