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Microstructured equaling

The microstructure at position (ii) consisted of grains of ferrite and colonies of pearlite. It was noticed that the pearlite had started to "spheroidise" (see Problem 5.2). The microstructure at position (i) consisted of grains of ferrite and grains of lower bainite in roughly equal proportions. Estimate the temperatures to which the tube been heated at positions (i) and (ii). Explain the reasoning behind your answers. [Pg.142]

The platelets comprise an array of parallel micro channels with microstructured triangular-shaped headers at both ends. In the headers holes form conducts to the external feed fluid supply. Optimization of the shape of the header with respect to flow equalization was the topic of various simulation studies [52, 53]. [Pg.270]

The deposition rate increases upon increasing the pressure. This is explained by noting that the impingement rate per unit area, r,, of molecules on the filament is linearly dependent on the pressure as r, = pj 2nksT, with the gas temperature. However, as the pressure becomes higher, the collisional mean free path of the silane becomes smaller, and the silane supply to the filaments becomes restricted. Moreover, the transport of deposition precursors to the substrate is restricted as well. The mean free path of silane was estimated to be 2.5 cm at a pressure of 0.02 mbar [531]. i.e.. the mean free path about equals the distance between filament and substrate. Indeed, a maximum in deposition rate is observed at this pressure. This corresponds to a value of pdk of 0.06 (cf. [530]). The microstructure parameter plotted as a function of pd has a minimum around Ms = 0.06 0.02 [530]. [Pg.160]

The gas chromatographic analysis of the unreacted monomers in the experiments from Table II discloses a constant C5/C8 ratio comparing the starting comonomer composition to the final composition. This means that monomer conversion is the same for 1,5-cyclooctadiene and cyclopentene in the copolymerization so that copolymer compositions are equal to the charge ratios. This result is consistent with the product analysis by 13C NMR spectroscopy where the copolymer composition is nearly identical to the starting comonomer composition. 13C NMR is used to determine the composition of the cyclopentene/1,5-cyclooctadiene copolymers as part of a detailed study of their microstructure (52). The areas of peaks at 29-30 ppm (the pp carbon from cyclopentene units) and at 27.5 ppm (the four ap carbons from the 1,5-cyclooctadiene) are used to obtain the mole fractions of the two comonomers (53, 54, 55). 13C NMR studies and copolymer composition determinations are described by Ivin (51, 56, 57) for various systems. [Pg.160]

The frozen sample is transferred into a freeze-fracture apparatus and processed at — 100°C at a vacuum between 10 and 5 X 10 bar. Within a homogeneous material the fracture happens randomly because all structural elements have equal probabilities for fracture. However, even a homogeneous material often consists of more or less polar areas. Within the polar areas, stronger interactions via hydrogen bonds prevent the fracture, which is thus less probable than the fracture within apolar areas. Therefore, the sample profile obtained after fracturing represents the microstructure of the sample only qualitatively but not quantitatively. [Pg.128]

It will be seen that there is an almost equal distribution of the charge between a and Y positions in THF for the heavier alkali metal counter-ions. If we suppose that increased charge produces an increased reactivity at a given position, then more vinyl unsaturation will be produced in THF than in hydrocarbon solvents and the highest vinyl content with heavier alkali metal counterions. The order in THF is however reversed, i.e. the highest, vinyl structures are produced by lithium catalysis (17) although microstructure determinations in this solvent normally apply to reactions with an appreciable free anion contribution and hence cannot be simply interpreted. In dioxane (18) and diethylether... [Pg.75]

The commerical polybutadiene (a highly 1,4 polymer with about equal amounts of cis and trans content) produced by anionic polymerization of 1,3-butadiene (lithium or organolithium initiation in a hydrocarbon solvent) offers some advantages compared to those manufactured by other polymerization methods (e.g., it is free from metal impurities). In addition, molecular weight distributions and microstructure can easily be modifed by applying appropriate experimental conditions. In contrast with polyisoprene, where high cis content is necessary for suitable mechanical properties, these nonstereoselective but dominantly 1,4-polybutadienes are suitable for practical applications.184,482... [Pg.776]

If the microstructure becomes ever finer by improved deposition technology, the domain irregularities should diminish. The SNR is limited by the shot noise of the laser source and is equal to R 0. In this region a high 0 is of great value. [Pg.147]

Point counting is the easiest way of determining the volume fraction of two or more phases in a microstructure. The volume fraction of a phase equals the fraction of points in an array that lies on that phase. A line count is another way of finding the volume fraction. If a series of lines are laid on a microstructure, the volume fraction of a phase equals the fraction of the total line length that lies on that phase. [Pg.4]

In summary, it is clear that there are substantial effects that vary systematically with the wavelength of the multilayer due both to internal stresses and the microstructure of the coatings. It has also been seen that deformation can occur not just by dislocation flow, as the initial analyses have assumed, but by mechanisms such as lattice rotations and shear along column boundaries. In addition, the use of indentation complicates the deformation field, so that the assumption that equal strains in both layers are required need not be correct. These effects all influence the hardness but have not so far been included in analyses. [Pg.236]

This coupled electrorotation mixer was actually not built as a complete device, but realized as a prototype version with simple microstructures, which were made by sputtering on to glass cover slips [95], By photolithography a small gap was etched in the middle of the coated slip to separate it into two equal halves. The latter are used as two electrodes of equal size. A wedge, freshly cut from the comer of a raw material piece, is placed on the gap as a kind of fixed microstructure to perform as the static dipole object so that an adjacent microsphere can be set into rotation. [Pg.24]

It is generally accepted that the soft-core RMs contain amounts of water equal to or less than hydration of water of the polar part of the surfactant molecules, whereas in microemulsions the water properties are close to those of the bulk water (Fendler, 1984). At relatively small water to surfactant ratios (Wo < 5), all water molecules are tightly bound to the surfactant headgroups at the soft-core reverse micelles. These water molecules have high viscosities, low mobilities, polarities which are similar to hydrocarbons, and altered pHs. The solubilization properties of these two systems should clearly be different (El Seoud, 1984). The advantage of the RMs is their thermodynamic stability and the very small scale of the microstructure 1 to 20 nm. The radii of the emulsion droplets are typically 100 nm (Fendler, 1984 El Seoud, 1984). [Pg.79]


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See also in sourсe #XX -- [ Pg.92 ]




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