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Summarizing Comparison

The success of any new technology depends on its correlation to established methodologies. Table 4 summarizes comparisons between dry reagent chemistries made by several manufacturers (44, 46, 56, 57) and conventional solution chemistries. In most cases, the correlation coefficients are greater than 0.95, with the slopes of the correlations close to unity. [Pg.56]

Table I summarizes comparisons between asphaltenes derived from bituminous coal liquefaction and those derived from petroleum crudes. The molecular size and atomic H/C ratios suggest a molecular profile quite different for the two asphaltenes. The ranges represent, as best as could be found, reasonable extremes for each of the properties. We are well aware that the number-average molecular weight of petroleum asphaltenes has been influenced by aggregate formation. To overcome this effect, molecular weight determinations should be made in dilute noninteracting solvents (e.g., methylene chloride), and solutions should be filtered or ultracentrifuged in helium-degassed solvents. Table I summarizes comparisons between asphaltenes derived from bituminous coal liquefaction and those derived from petroleum crudes. The molecular size and atomic H/C ratios suggest a molecular profile quite different for the two asphaltenes. The ranges represent, as best as could be found, reasonable extremes for each of the properties. We are well aware that the number-average molecular weight of petroleum asphaltenes has been influenced by aggregate formation. To overcome this effect, molecular weight determinations should be made in dilute noninteracting solvents (e.g., methylene chloride), and solutions should be filtered or ultracentrifuged in helium-degassed solvents.
The comparisons of the various methods of evaluation made in this Chapter are valid up to mid-1999, but the very rapid developments in the multimedia market will lead to further improvements in the future. A summarized comparison of quantitative evaluation methods for TLC up to the present time can be found in [124d]. [Pg.178]

A summarizing comparison for composites produced on a kilogram-scale with the two-step method described above including unnotched Charpy values and data for glass fiber reinforced PP is given in Fig. 18.25. [Pg.502]

Fig. 3.7 Summarized comparisons of G protein coupling and main and alternative signaling pathways for the four... Fig. 3.7 Summarized comparisons of G protein coupling and main and alternative signaling pathways for the four...
Table 3.1 Summarized comparison of function, G protein coupling and signaling pathways of histamine H, H2, H3, and H4 receptors ... Table 3.1 Summarized comparison of function, G protein coupling and signaling pathways of histamine H, H2, H3, and H4 receptors ...
Summarized comparisons of functions, indications for antagonists, G protein couphng, and signaling pathways for the four histamine receptors are shown in Table 3.1 and Fig. 3.7. [Pg.52]

A summarized comparison of the used oils was carried out by the distribution of rank numbers according to the outcome of each oil at the most important parameters for the assessment of the oils after a frying time of 72 h. The oil coming out on the top got a 1 while the worst oil had a 4. After distribution of the rank numbers, the mean value was calculated for each oil. For this assessment the following parameters, oligomer triacylglycerols, polar compounds, free fatty acids as weU as the sensory evaluation of the oil and the French fries were used. [Pg.208]

Some results obtained by the HMO method (one of the more useful for reactivities comparisons) are summarized in Tables III-17 and III-18. [Pg.358]

The thiazolyl radicals are, in comparison to the phenyl radical, electrophilic as shown by isomer ratios obtained in reaction with different aromatic and heteroaromatic compounds. Sources of thiazolyl radicals are few the corresponding peroxide and 2-thiazolylhydrazine (202, 209, 210) (see Table III-34) are convenient reagents, and it is the reaction of an alky] nitrite (jsoamyl) on the corresponding (2-, 4-, or 5-) amine that is most commonly used to produce thiazolyl radicals (203-206). The yields of substituted thiazole are around 40%. These results are summarized in Tables III-35 and IIT36. [Pg.370]

These and similar rankings based on more extensive comparisons are summarized in terms of substituents in Table 7.3. [Pg.438]

A broad comparison of the main types of processes, the strength and quaUty of phosphoric acid, and the form and quaUty of by-product calcium sulfate are summarized in Table 7. Because the dihydrate process is the most widely used, the quaUty of its acid and calcium sulfate and its P2O3 recovery are taken as reference for performance comparisons. Illustrative flow diagrams of the principal variations in process types have been pubUshed (39). Numerous other variations in process details ar also used (40—42). The majority of plants use a dihydrate process and some of these have production capacity up to 2100 of P2O3 per day. [Pg.225]

As a general rule the sulfenamides exhibit faster cure rate than the thiazoles. If secondary accelerators are used, dithiocarbamates are scorchiest and give the fastest cure followed by the thiurams, then the guanidines. Figure 6 summarizes these comparisons to show a series of natural mbber (NR) recipes using either a thiazole (MBTS) or sulfenamide (TBBS) primary accelerator in combination with the various secondary accelerators (21). In this study, the initial primary accelerator levels were selected to produce nearly equivalent modulus or state of cure in the NR. [Pg.237]

Except for the addiction HabiUty of some of the narcotic antitussives, side effects for most of the centrally acting compounds are relatively few and mild at therapeutic doses. QuaUtative comparisons of both side effects and pharmacological profiles have been summarized for many of the compounds described above (97). [Pg.527]

Whilst comparisons of literature data are sometimes difficult to make as a result of experimental differences and marked solvent effects, several energy barriers (AG ) which reflect the different substituent effects are summarized in Table 1. [Pg.52]

Comparisons on the basis of interest can be summarized as (1) the net present value (NPV) and (2) the discounted-cash-flow rate of return (DCFRR), which from Eqs. (9-53) and (9-54) is given formally as the fractional interest rate i which satisfies the relationship... [Pg.815]

Ruthven (gen. refs.) summarizes methods for the measurement of effective pore diffusivities that can be used to obtain tortuosity factors by comparison with the estimated pore diffusion coefficient of the adsorbate. Molecular diffusivities can be estimated with the methods in Sec. 6. [Pg.1511]

Pai+icle size enlargement equipment can be classified into several groups, with advantages, disadvantages, and applications summarized in Table 20-36. Comparisons of bed-agitation intensity, compaction pressures, and product bulk density for selected agglomeration processes are highlighted above in Fig. 20-71. [Pg.1891]

In. sclcciing an exchanger, one must know the advantages and disadvantages td each type. The three basic types of shell-and-tube exchangers are fixed tube sheet, floating head, and U-tube, Table 3-1 summarizes the comparison between these three exchangers. [Pg.57]

Table 9.7 summarizes the comparison of SEC column performance with regard to particle size of the packing material. The author tried to create this table using the test results of different manufacturers of styrene-divinyl-benzene columns. [Pg.279]

All jobs were run using the 6-31G(d) basis set. Our results are summarized in the following table, which also presents HF and MP2 values for comparison ... [Pg.120]

An alternative form of the right-handed double helix is A-DNA. A-DNA molecules differ in a number of ways from B-DNA. The pitch, or distance required to complete one helical turn, is different. In B-DNA, it is 3.4 nm, whereas in A-DNA it is 2.46 nm. One turn in A-DNA requires 11 bp to complete. Depending on local sequence, 10 to 10.6 bp define one helical turn in B-form DNA. In A-DNA, the base pairs are no longer nearly perpendicular to the helix axis but instead are tilted 19° with respect to this axis. Successive base pairs occur every 0.23 nm along the axis, as opposed to 0.332 nm in B-DNA. The B-form of DNA is thus longer and thinner than the short, squat A-form, which has its base pairs displaced around, rather than centered on, the helix axis. Figure 12.13 shows the relevant structural characteristics of the A- and B-forms of DNA. (Z-DNA, another form of DNA to be discussed shortly, is also depicted in Figure 12.13.) A comparison of the structural properties of A-, B-, and Z-DNA is summarized in Table 12.1. [Pg.367]

All 12 compounds are well known and are available commercially their physical properties are summarized in Table 13.6 Comparisons with the corresponding data for NX3 (p. 438) and PX3 (p. 496) are also instructive. Trends in mp, bp and density are far from regular and reflect the differing structures and bond types. [Pg.558]


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