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Mixing analysis

P 12] The mixing performance was analyzed by a dilution-type experiment. Here, water and the fluorescent dye uranine, sodium fluorescein [22], The latter is water-soluble. External pressure was applied to the liquids using a fluid dispenser. The flow rates of both water and the aqueous uranine solution were 5 pi min-1. A fluorescent microscope with a digital CCD camera with a 1.25x objective was used for optical mixing analysis. Fluorescent filters at 460-490 and 515-550 nm... [Pg.42]

Similar very good agreement was found for a quantitative mixing analysis when determining the diffusive widths at various locations along the mixing channel and for various flow rates [70], Thus, the use of the confocal fluorescence technique for complex mixing analysis was demonstrated and compared with the potential of... [Pg.79]

For all calibration solutions, the retention times of the isomers must fall within the appropriate retention time windows established by the window defining mix analysis. In addition, the absolute retention times of the recovery standards, 13Ci2-1,2,3,4-TCDD and 13Ci2-1,2,3,6,7,8-HxCDD, shall not change by more than 10 seconds between the initial CC3 analysis and die analysis of any other standard. [Pg.455]

Rixen, T., and Ittekkot, V. (2005). Nitrogen deficits in the Arabian Sea, implications from a three component mixing analysis. Deep-Sea Res. II 52, 1879-1891. [Pg.678]

An Introduction to Photoelectron Spectroscopy. By Pradip k. Ghosh Room Temperature Phosphorimetry for Chemical Analysis. By Tuan Vo-Dinh Potentiometry and Potentiometric Titrations. By E. P. Serjeant Design and Application of Process Analyzer Systems. By Paul E. Mix Analysis of Organic and Biological Surfaces. Edited by Patrick Echlin Small Bore Liquid Chromatography Columns Their Properties and Uses. Edited by Raymond P. W. Scott... [Pg.437]

The second extraction step, separation of the two phases into the raffinate and extract streams, will be considered next. This step, when combined with the previous mixing analysis, constitutes one ideal equilibrium stage. Imagine (Figure 3.23) that a mixing is followed by an equilibrium stage which allows F to separate into two streams Vo and Oo, which are in equilibrium. [Pg.61]

Kang, T. G., Kwon, T. H. Colored particle tracking method for mixing analysis of chaotic micromixers, J. Micromech. Microeng. 14, (2004) 891-899. [Pg.77]

Comparisons between devices are complicated by the effect of initial distribution on mixing effectiveness. If initial distributions are significantly different, care must be taken when making any device comparisons, even when the mixing analysis scheme and applied mixing measure are the same. One approach is to characterize the mixing performance of a device for several relevant initial distributions, a practice that has not been standard in the evaluation of microfluidic mixers. [Pg.2266]

Ponhong, K., N. Teshima, K. Grudpan, S. Motomizu, and T. Sakai. 2011. Simultaneous injection effective mixing analysis system for the determination of direct bilirubin in urinary samples. Talanta 87 113-117. [Pg.130]

Teshima, N., D. Noguchi, Y. Joichi et al. 2010. Simultaneous injection-effective mixing analysis of palladium. Anal. Sci. 26 143-144. [Pg.130]

Bockhom H, Mewes D, Peukert W, Wamecke H-J Micro and macro mixing analysis, simulation and numerical calculation, Heidelberg, 2010, Springer. [Pg.72]

Shah RSSRE, Sajjadi B, Raman AAA, Ibrahim S Solid-liquid mixing analysis in stirred vessels, Rev Chem Eng 31 119-147, 2015. http //dx.doi.org/10.1515/revce-2014-0028. [Pg.351]


See other pages where Mixing analysis is mentioned: [Pg.264]    [Pg.253]    [Pg.399]    [Pg.8]    [Pg.628]    [Pg.642]    [Pg.1882]    [Pg.2182]    [Pg.56]    [Pg.171]    [Pg.283]    [Pg.398]    [Pg.226]    [Pg.404]    [Pg.213]    [Pg.2264]    [Pg.457]    [Pg.51]    [Pg.611]    [Pg.1279]    [Pg.121]    [Pg.122]    [Pg.122]    [Pg.258]    [Pg.27]    [Pg.310]   
See also in sourсe #XX -- [ Pg.388 ]

See also in sourсe #XX -- [ Pg.92 ]




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