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Variation of contrast

Certain solutions consist of two solvents s/ = 0, 1 and of several solutes (m 2). Then, it is appropriate to contrast a solute with respect to the solvent mixture. We shall consider the case where the two solvents are isotopes of each other and we shall assume that each species has the same molecular volume cs. [Pg.257]

The contrast length of a solute s/ with respect to the mixture of solvents is [Pg.257]

A detailed calculation, similar to the one solvent calculation gives the result [Pg.257]

By changing the composition of the solvent, we modify x and therefore also the contrast length b (x). This is the method of variation of contrast.8,9 [Pg.257]


The last three chapters have involved a certain amount of mathematical slog. But it is worth it. These chapters have introduced the concepts governing the interaction of acoustic waves with specimens, the origin of the contrast in acoustic microscopes (especially the variation of contrast with defocus), and how the transition can be made from obtaining images to being able to interpret them quantitatively. And now the time has come to look at some of those pictures. [Pg.159]

The variation of contrast with defocus can be illustrated by a series of snapshots from the examination of another caries lesion, this time one that had occurred naturally in a tooth (Peck and Briggs 1987). The sequence in Fig. 9.11 shows what would be seen over the shoulder of the microscopist as he... [Pg.183]

Fig. 7.5 Variation of contrast (schematic) by alteration of the isotopic composition of the solvent (e.g. H20/D20 mixture according to Ballauff et al.)... Fig. 7.5 Variation of contrast (schematic) by alteration of the isotopic composition of the solvent (e.g. H20/D20 mixture according to Ballauff et al.)...
Variation of contrast [46] is an important experimental technique in neutron small-angle scattering. Above and beyond size determination, it affords detailed insights into the internal structure of dissolved dendrimers and even permits the location of selected components of the molecule which have been previously labelled with deuterium. [Pg.268]

During the last decade, numerous reports have appeared of linear defects in GBs in metals observed by TEM. The observed variation in geometry as well as the variation of contrast for various diffracting conditions indicate that a single type of defect cannot account for all the observations. Among the numerous interpretations that have been suggested for the linear defects are (i) absorbed lattice dislocations (ii) steps, at least a few unit cells high, in the boundary plane (iii) structural dislocations in the boundary that accommodate small deviations from the special orien-... [Pg.145]

Apparent mean square radius and variation of contrast Let us expand Happ(q) in the vicinity of q = 0. We get... [Pg.282]

Next, consider the behavior of the shadow. As seen in Fig. 3, the threshold voltage of the shadow region varies relatively little taking on values between 0 8 and 1 2 volts. The shadow also exhibits relatively minor variations of contrast with polar angle when measured at 3, 6, and 10 volts as shown in Figs. 4, 5, and 6, respectively. [Pg.247]

We noted above that the presence of monomer with a functionality greater than 2 results in branched polymer chains. This in turn produces a three-dimensional network of polymer under certain circumstances. The solubility and mechanical behavior of such materials depend critically on whether the extent of polymerization is above or below the threshold for the formation of this network. The threshold is described as the gel point, since the reaction mixture sets up or gels at this point. We have previously introduced the term thermosetting to describe these cross-linked polymeric materials. Because their mechanical properties are largely unaffected by temperature variations-in contrast to thermoplastic materials which become more fluid on heating-step-growth polymers that exceed the gel point are widely used as engineering materials. [Pg.314]

Using combustion to stimulate bitumen production is attractive for deep reservoirs and in contrast to steam injection usually involves no loss of heat. The duration of the combustion may be short (days) depending on requirements. In addition, backflow of oil through the hot 2one must be prevented or excessive coking occurs (15,16). Another variation of the combustion process involves use of a heat-up phase, then a blow-down (production) phase, followed by a displacement phase using a fire-water flood (COFCAW process). [Pg.357]

The pursuit of further miniaturization of electronic circuits has made submicrometer resolution Hthography a cmcial element in future computer engineering. LB films have long been considered potential candidates for resist appHcations, because conventional spin-coated photoresist materials have large pinhole densities and variations of thickness. In contrast, LB films are two-dimensional, layered, crystalline soHds that provide high control of film thickness and are impermeable to plasma down to a thickness of 40 nm (46). The electron beam polymerization of CO-tricosenoic acid monolayers has been mentioned. Another monomeric amphiphile used in an attempt to develop electron-beam-resist materials is a-octadecylacryUc acid (8). [Pg.534]

In contrast with the dc source, more variables are needed to describe the rf source, and most of these cannot be measured as accurately as necessary for analytical application. It has, however, been demonstrated that the concept of matrix-independent emission yields can continue to be used for quantitative depth-profile analysis with rf GD-OES, if the measurements are performed at constant discharge current and voltage and proper correction for variation of these two conditions are included in the quantification algorithm [4.186]. [Pg.226]

The work of Hyatt on cyclotriveratrylene—derived octopus molecules contrasts with this. Of course, these species have the advantage of ligand directionality absent in the benzene-derived octopus molecules. Except for the shortest-armed of the species (i.e., n = 1), all of the complexing agents (i.e., n = 2—4) were capable of complexing alkali metal cations. Synthesis of these species was accomplished as indicated below in Eq. (7.7). These variations of the original octopus molecules were also shown to catalyze the reaction between benzyl chloride and potassium acetate in acetonitrile solution and to effect the Wittig reaction between benzaldehyde and benzyltriphenylphos-phonium chloride. [Pg.315]

Let us underline some similarities and differences between a field theory (FT) and a density functional theory (DFT). First, note that for either FT or DFT the standard microscopic-level Hamiltonian is not the relevant quantity. The DFT is based on the existence of a unique functional of ionic densities H[p+(F), p (F)] such that the grand potential Q, of the studied system is the minimum value of the functional Q relative to any variation of the densities, and then the trial density distributions for which the minimum is achieved are the average equihbrium distributions. Only some schemes of approximations exist in order to determine Q. In contrast to FT no functional integrations are involved in the calculations. In FT we construct the effective Hamiltonian p f)] which never reduces to a thermo-... [Pg.807]

The mechanism depicted in Scheme 28 accounts for the formation of the ringopening products (97JOC8325). It is a variation of the RCRE mechanism. By contrast, on irradiation l-methyl-5-phenylpyrazole (75) gave 76, 77, and 78 (Scheme 29) (97JOC8325). Compounds 76 and 77 can be obtained via an ICI... [Pg.65]

A variation of the general method for the synthesis of 2-amino-selenazoles is to avoid the use of the free a-halogenocarbonyl compound and in its place react the corresponding ketone and iodine with selenourea.This procedure is also taken from thiazole chemistry. By contrast with thiourea, the reaction with selenourea needs a longer reaction time and the work up of the reaction mixture is somewhat more difficult. Usually an excess of the ketone is used. In the preparation of 2-amino-4-( n-nitrophenyl)selenazole, a very high yield, calculated on the amount of iodine used, was obtained. To explain this peculiar result, the oxidative action of the nitro group was invoked. This liberates free iodine from some of the hydrogen iodide eliminated in the condensation reaction, and the free iodine then re-enters into the reaction. [Pg.348]

One of the signatures of densely tethered chains is expressed in Eq. 5, namely the linear variation of L with N. This stands in marked contrast with free chains where excluded volume interaction produces, at most, an R N3/5 distortion from the R N1/2 unperturbed dimensions. Tethered layers are stretched and this is the origin of their interesting behavior. [Pg.38]

Two key parameters have been found to determine the ultimate eapabili-ties of the MOEMS-based MOS contrast and spectral photometric variation (SPV). Contrast is dehned as the total amount of non-selected flux of light passing through the multi-slit device a contrast requirement of 2000 has been established in order to avoid pollution of the spectra by strong sources (spoilers) and sky background. The SPV is the unpredictable photometric variation due to the random position of the sources on the PMSM grid SPV requirement has been fixed to <10%. [Pg.112]

The fringes contrasts are subject to degradation resulting from dissymmetry in the interferometer. The optical fields to be mixed are characterized by a broadband spectrum so that differential dispersion may induce a variation of the differential phase over the spectrum. Detectors are sensitive to the superposition of the different spectral contributions. If differential dispersion shifts the fringes patterns for the different frequency, the global interferogramme is blurred and the contrast decreases. Fig. 5 shows corresponding experimental results. [Pg.295]


See other pages where Variation of contrast is mentioned: [Pg.171]    [Pg.61]    [Pg.245]    [Pg.257]    [Pg.247]    [Pg.251]    [Pg.171]    [Pg.61]    [Pg.245]    [Pg.257]    [Pg.247]    [Pg.251]    [Pg.180]    [Pg.445]    [Pg.526]    [Pg.564]    [Pg.1371]    [Pg.279]    [Pg.140]    [Pg.356]    [Pg.442]    [Pg.473]    [Pg.121]    [Pg.294]    [Pg.59]    [Pg.220]    [Pg.8]    [Pg.778]    [Pg.1180]    [Pg.437]    [Pg.117]    [Pg.185]    [Pg.153]    [Pg.168]    [Pg.134]    [Pg.202]    [Pg.327]   


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