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Extractants single 21, Table

Table I gives the values of the extraction factor (a) required for americium removals ranging from 80 to 99%. These required values of a are given for the three modes of extraction (single-contact, two stage crosscurrent, and two stage countercurrent). Table I gives the values of the extraction factor (a) required for americium removals ranging from 80 to 99%. These required values of a are given for the three modes of extraction (single-contact, two stage crosscurrent, and two stage countercurrent).
The above is not the only possible or even plausible index of chirality that can be extracted for Table 32. Rather than exploring alternatives, let us emphasize the significance of the approach outlined. The main result of our scheme is to assign to chiral structures a sequence, not a single index. Thus, the two most chiral benzenoids C and L are represented by the respective sequences... [Pg.227]

B-adducts involve the -carbon atom endo/exo notation, as usual, defines the di-astereoisomeric relation of the C-N-0 nitrone-group with respect to the substi-tuent(s). The isomer definition is made clearer in the transition structures which are taken to be "concerted according to the extant literature. One can see that all the adducts allowed are present in the reaction mixture with variable, but non negligible fractions. The same is true for the reactions of 3,4-dihydro-isoquinoline-N-oxide and C-phenyl-N-methylnitrone,3 whereas the reactions of N-H-nitrone (H-nitrone), N-Me-nitrone and N-(t)-Bu-nitrone3t>.c lead to a single adduct, which, in our notation, is the B-regioadduct (Scheme 3). The experimental trends extracted from Tables 1-2 and from the cited literature can be summarised as follows ... [Pg.153]

In addition to qualitative analysis of nearly all the elements of the periodic table, EEL spectra also enable determination of the concentration of a single element which is part of the transmitted volume and hence gives rise to a corresponding ionization edge. As in all comparable spectroscopic techniques, for quantification the net edge signal, which is related to the number N of excited atoms, must be extracted from the raw data measured. The net intensity 4 of the feth ionization shell of an individual element is directly connected to this number, N, multiplied by the partial cross-section of ionization ) and the intensity Iq of the incident electron beam, i.e. ... [Pg.65]

When the products are partially or totally miscible in the ionic phase, separation is much more complicated (Table 5.3-2, cases c-e). One advantageous option can be to perform the reaction in one single phase, thus avoiding diffusional limitation, and to separate the products in a further step by extraction. Such technology has already been demonstrated for aqueous biphasic systems. This is the case for the palladium-catalyzed telomerization of butadiene with water, developed by Kuraray, which uses a sulfolane/water mixture as the solvent [17]. The products are soluble in water, which is also the nucleophile. The high-boiling by-products are extracted with a solvent (such as hexane) that is immiscible in the polar phase. This method... [Pg.264]

Historically, the development of animal cell culture systems has been dependent upon the development of new types of tissue culture media. Mouse L cells and HeLa cells were developed using a balanced salt solution supplemented with blood plasma, an embryonic tissue extract, and/or serum. In 1955 Eagle developed a nutritionally defined medium, containing all of the essential amino acids, vitamins, cofactors, carbohydrates, salts, and small amounts of dialyzed serum (Table 1). He demonstrated that this minimal essential medium (MEM) supported the long-term growth of mouse L and HeLa ceils. Eagle s MEM was so well defined that the omission of a single essential nutrient eventually resulted in the death of these animal cells in culture. [Pg.471]

This sometimes complicates the extraction of molecular weight data as it is not always immediately clear which ions in the spectrum originate from each component. This can be determined by the use of equation (4.6). An example of this is shown in Figure 4.18, which shows the electrospray spectrum from what is apparently a single chromatographic response, while Table 4.3(a) displays the results of applying equation (4.6) to the major ions found in that spectrum. As... [Pg.173]

Purification of the radioactive tracer was modified to include a fractional sublimation before a single extraction—recrystallization cycle to conserve the tracer material. Microgram samples were prepared in melting point capillaries for assay by mass spectroscopic analysis (Table III), made by direct probe injection of the sample into the ion source (18). The probe was heated rapidly to 200°C, and mass spectra were obtained during vaporization of the sample. Tri-, tetra-, and pentachlorodibenzo-p-dioxins vaporized simultaneously with no observed fractionation. [Pg.5]

The total anthocyanin content can often be determined in crude extracts containing other phenolic materials by measuring absorptivity of the solution at a single wavelength (Table 6.3.1). This is possible because anthocyanins have typical absorption bands in the 490 to 550 nm region of the visible spectra — far from the absorption bands of other phenolics with spectral maxima in the UV range. ... [Pg.483]

Blending of Coals. In practice it is unlikely that a coal from a single source will be used as a feed to a large solvent extraction plant and a blend of several coals may have to be used. A preliminary series of tests using blends gave extraction yields in reasonable agreement with those derived from extraction of individual coals (Table VII). [Pg.131]


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See also in sourсe #XX -- [ Pg.2 , Pg.6 ]




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Selective chemical extraction single extractants 21, Table

Single extraction

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