We report the first use of stray field magnetic resonance imaging in the determination of concentration profiles in layers (with submillimeter thickness) of coarse oil-in-water emulsions that are undergoing creaming. We compare our results for emulsions having various oil contents to the predictions of a numerical model. In emulsions having low oil content (12 and 23 vol %), we find that the model adequately predicts the profile shape and time-dependent change in the lower region of the emulsion. In the cream layer at the top of each of the samples, however, the predictions of the model deviate substantially from the observed profiles. Whereas the model assumes that the concentration of oil in the cream layer is constant as the layer increases in thickness, we observe that there is a concentration gradient in the cream layer and that the concentration of oil in the layer increases with time. In explaining our findings, we consider the effects of polydispersity and the presence of gum xanthan in the continuous phase and also the possibility of gradual compaction of oil droplets in the cream layer (a phenomenon not considered in the model).
The quantitative analysis of mixtures of sulfur-containing gases such as those emitted from the stack of a kraft pulp mill is best performed by the use of a gas chromatograph. The degree of success depends primarily upon the type of solid support, stationary phase, column material, and detector used. Up to now, various packings with different stationary phases have been tried with little or partial success.
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