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Other Mixing Techniques

These latter techniques are especially useful for large comets where having one-half the usually required water present aids in drying, and therefore limits wet destruction of the metals. This is very useful with magnalium. [Pg.64]

These techniques can obviously be combined with the previously mentioned marbling with delay reagents, meal powder marbling and the flake aluminum technique to build very complex structures ofpyrotechnic utility. [Pg.64]


Two other conventional techniques may be also used for a supported catalyst preparation [6]. One includes mixing of a ME and a support via ACF dipping into the formed ME. In the second one, THF is added during this mixing to release nanoparticles. [Pg.294]

Other chromatographic techniques that have been applied to the tetracyclines, including CTC, involve low pressure column chromatography. Ascione et al. (64) developed a semiautomated system whereby sample solutions are automatically injected onto a column of diatomaceous earth mixed with... [Pg.127]

Other preharvest techniques include the development of more resistant crops (e.g., Becker, 1999 Guo et al., 1998), and biological control with atoxigenic A. flavus strains (Cotty, 1990 Dorner et al., 1998). Atoxigenic A. jiavus competed successfully with a toxic isolate when they were grown in mixed culture, obtaining a reduction of the aflatoxin content by 82 to 100%. This is a worthwhile approach for control, however possible side effects caused by a preemptive application of A. jiavus in the environment must be studied to determine potential risks to human and animal health. [Pg.234]

What differentiates CVD from other evaporation techniques is that growth units, the fundamental bricks essential for growth, are chemically generated at the mixing zone. The formation of growth units implies either chemical reaction of the... [Pg.125]

Other deposition techniques have been used (35) and a promising technique of chemical vapor deposition has been reported and substantial critical current densities obtained by Berry et al. (39) and by Watanabe et al. (40). Values of Jc at 77 K and at 2 T and 27 T were 4 x 105 and 6.5 x 104 A/cm2 respectively (40). The surface of the film shows significant growth of c axis material in the plane as well as the desired normal to the plane growth. On the other hand this mixed phase growth may supply additional pinning centers for the improved critical current. [Pg.646]

The description of pump-probe signals presented in the preceding section can be immediately generalized to heterodyne-detected transient grating spectroscopy as well as to other four-wave mixing techniques. Heterodyne detection involves mixing the scattered field with an additional heterodyne field 4(r). The signal in the ks direction can then be written in terms of the polarization Ts(t) as... [Pg.358]

The last of these methods has been applied particularly to chemical reaction vessels. It is covered in detail in Chapter 17. In most cases, however, the RTDs have not been correlated with impeller characteristics or other mixing parameters. Largely this also is true of most mixing investigations, but Figure 10.3 is an uncommon example of correlation of blend time in terms of Reynolds number for the popular pitched blade turbine impeller. As expected, the blend time levels off beyond a certain mixing intensity, in this case beyond Reynolds numbers of 30,000 or so. The acid-base indicator technique was used. Other details of the test work and the scatter of the data are not revealed in the published information. Another practical solution of the problem is typified by Table 10.1 which relates blend time to power input to... [Pg.290]

In this case, the electrogenerated R will encounter Z as it diffuses away from the electrode and will react to form P. This diffusional mixing of two reactants (R and Z in this example) is the basis for chronoabsorptometry (and other electrochemical techniques) as a kinetic method. The homogeneous chemical reaction of R will perturb its accumulation by a magnitude that is proportional both to k and to the concentration of Z. The influence of this perturbation is apparent from the concentration-distance profiles for R, which are illustrated for a rate constant of 107 L/(mol s) in Figure 3.9. [Pg.66]

Attempts to synthesize C-terminal peptide aldehydes using other reductive techniques are less successful. 24"29 The reduction of a-amino acid esters with sodium amalgam and lithium aluminum hydride reduction of tosylated a-aminoacyldimethylpyrazoles resulted in poor yields. 26,29 The Rosemond reduction of TV-phthaloyl amino acid chlorides is inconvenient because the aldehyde is sensitive to hydrazine hydrate that is used to remove the phthaloyl group. 27 28 jV -Z-Protected a-aminoacylimidazoles, which are reduced to the corresponding aldehydes using lithium aluminum hydride, are extremely moisture sensitive and readily decomposed. 25 The catalytic reduction of mixed carbonic/carboxylic acid anhydrides, prepared from acylated a-amino acids, leads to poor reproducibility and low yields. 24 The major problems associated with these techniques are overreduction, racemization, and poor yields. [Pg.200]

Matrix solid-phase dispersion (MSPD) is the extraction method of choice for the analysis of solid samples, such as plant material, foodstuffs or tissue samples [26]. This method has been developed especially for solid or viscous matrices. MSPD is preferable to other extraction techniques, because the solid or viscous sample can be directly mixed with the sorbent material of the stationary phase [27]. As the carotenoid stereoisomers stay bound in their biological matrix until the elution step, they are protected against isomerisation and oxidation [28]. The extraction scheme of MSPD is shown in Figure 5.2.1. [Pg.130]

In these studies a dynamic testing method (the mixing-cell) has been used to measure the sorption kinetics of 4 different radionuclides on Lac du Bonnet granite from the Archean Superior Province of the Canadian Shield. This method has been used previously (2) for measurement of sorption kinetics without the interference of hydraulic dispersion common in many other dynamic techniques. [Pg.49]


See other pages where Other Mixing Techniques is mentioned: [Pg.73]    [Pg.73]    [Pg.64]    [Pg.123]    [Pg.229]    [Pg.73]    [Pg.73]    [Pg.64]    [Pg.123]    [Pg.229]    [Pg.258]    [Pg.356]    [Pg.200]    [Pg.382]    [Pg.25]    [Pg.136]    [Pg.388]    [Pg.587]    [Pg.150]    [Pg.330]    [Pg.238]    [Pg.295]    [Pg.96]    [Pg.65]    [Pg.42]    [Pg.304]    [Pg.142]    [Pg.558]    [Pg.547]    [Pg.74]    [Pg.468]    [Pg.50]    [Pg.289]    [Pg.172]    [Pg.353]    [Pg.362]    [Pg.254]    [Pg.89]    [Pg.170]    [Pg.179]    [Pg.331]    [Pg.195]    [Pg.34]    [Pg.270]   


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Mixing techniques

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