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Experiments synthesis

A possible problem of sealing the electrolyte path is found in the Foreman and Veatch cell. This can be avoided by placing the cells in a vessel. The best known example of this is the Beck and Guthke cell shown in Figure 8 (74). The cell consists of a stack of circular bipolar electrodes in which the electrolyte is fed to the center and flows radially out. Synthesis experience using this cell at BASF has been described (76). This cell exhibits problems of current by-pass at the inner and outer edge of the disk cells. Where this has become a serious problem, insulator edges have been fitted. The cell stack has parallel electrolyte flow however, it is not readily adaptable to divided cell operation. [Pg.91]

Only parts needed above but for the vapor-phase reactor are listed here. Most of the description for the installation for methanol synthesis experiments (Figure 4.2.1) holds for this installation, too. In the mentioned unit, product was blown down while still hot, thus keeping all product in a single vapor phase. This simplifies material balance calculations. When avoiding condensation is difficult, cooling and separation becomes necessary. This method was used in the cited AIChEJ publication. [Pg.89]

C2. Calculation of Operating conditions and Transport Criteria for the UCKRON Test Problem as a Methanol Synthesis Experiment in the Rotoberty ... [Pg.221]

Shock-synthesis experiments were carried out over a range of peak shock pressures and a range of mean-bulk temperatures. The shock conditions are summarized in Fig. 8.1, in which a marker is indicated at each pressure-temperature pair at which an experiment has been conducted with the Sandia shock-recovery system. In each case the driving explosive is indicated, as the initial incident pressure depends upon explosive. It should be observed that pressures were varied from 7.5 to 27 GPa with the use of different fixtures and different driving explosives. Mean-bulk temperatures were varied from 50 to 700 °C with the use of powder compact densities of from 35% to 65% of solid density. In furnace-synthesis experiments, reaction is incipient at about 550 °C. The melt temperatures of zinc oxide and hematite are >1800 and 1.565 °C, respectively. Under high pressure conditions, it is expected that the melt temperatures will substantially Increase. Thus, the shock conditions are not expected to result in reactant melting phenomena, but overlap the furnace synthesis conditions. [Pg.181]

Four different material probes were used to characterize the shock-treated and shock-synthesized products. Of these, magnetization provided the most sensitive measure of yield, while x-ray diffraction provided the most explicit structural data. Mossbauer spectroscopy provided direct critical atomic level data, whereas transmission electron microscopy provided key information on shock-modified, but unreacted reactant mixtures. The results of determinations of product yield and identification of product are summarized in Fig. 8.2. What is shown in the figure is the location of pressure, mean-bulk temperature locations at which synthesis experiments were carried out. Beside each point are the measures of product yield as determined from the three probes. The yields vary from 1% to 75 % depending on the shock conditions. From a structural point of view a surprising result is that the product composition is apparently not changed with various shock conditions. The same product is apparently obtained under all conditions only the yield is changed. [Pg.182]

Compound Registration. A common step in a chemical synthesis experiment is the reaction of one or more existing molecules to form a desired product. This necessitates selecting molecules from a chemical database or repository and registering the target molecule into that same chemical database or... [Pg.222]

Several factors indicate that the amino acids detected in all of these carbonaceous chondrites are indigenous and that they must have originated abiotically. First, the presence of protein and non-protein amino acids, with approximately equal quantities of D and L enantiomers points to a nonbiological origin and precludes terrestrial contamination. In addition, the non-extractable fraction of the Murchison is significantly heavier in 13C than terrestrial samples. Finally, the relative abundances of some compounds detected resemble those of products formed in prebiotic synthesis experiments. The aliphatic hydrocarbons are randomly distributed in chain length, and the C2, C3, and C4 amino acids have the highest concentrations (i.e., the most easily synthesized amino acids with the least number of possible structures are most abundant) [4]. [Pg.391]

Your laboratory experiments can be classified to two major types a technique experiment or a synthesis experiment. Each requires different handling. [Pg.9]

In a synthesis experiment, the point of the exercise is to prepare a clean sample of the product you want. All the operations in the lab (e.g., distillation,... [Pg.9]

Using the TLC concept to prepare pure substances for use in other experiments, such as standards preparation or synthesis experiments, is possible. This is called preparatory TLC and involves a thicker layer of stationary phase so that larger quantities of the mixture can be spotted and a larger quantity of pure component obtained. [Pg.317]

The omnipresence of aluminium in weathering environments results in most of the Fe oxides in soils, except lepidocrocite, being Al-substituted. The possible range of substitution as deduced from synthesis experiments (see Chap. 3) viz. up to Al/ (Fe Al) of ca. 0.33 in goethite and up to Al/(Fe Al) of ca. 0.16 in hematite is also found in soil goethites and hematites. Where the two oxides coexist on a small scale... [Pg.456]


See other pages where Experiments synthesis is mentioned: [Pg.218]    [Pg.85]    [Pg.257]    [Pg.180]    [Pg.189]    [Pg.210]    [Pg.835]    [Pg.92]    [Pg.238]    [Pg.238]    [Pg.388]    [Pg.9]    [Pg.9]    [Pg.11]    [Pg.13]    [Pg.14]    [Pg.15]    [Pg.15]    [Pg.16]    [Pg.17]    [Pg.17]    [Pg.18]    [Pg.19]    [Pg.19]    [Pg.27]    [Pg.20]    [Pg.380]    [Pg.401]    [Pg.166]    [Pg.446]    [Pg.447]    [Pg.449]    [Pg.451]    [Pg.458]    [Pg.498]   
See also in sourсe #XX -- [ Pg.9 , Pg.13 , Pg.14 , Pg.15 , Pg.16 , Pg.17 , Pg.18 ]

See also in sourсe #XX -- [ Pg.13 , Pg.18 , Pg.19 , Pg.20 , Pg.21 , Pg.22 ]




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