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In a first step, the most important parameters for the separations were determined and studied for their effects by means of experimental designs.
The maceral compositions of products from density separations were determined by Zeiss Imager A2 m microscope according to ISO 7404-3 (Methods for the petrographic analysis).
The proximate analyses, total sulfurs and the concentrations of mercury of the raw coals and products from density separations were determined as described in Chapter 2.1.1.
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Optimum conditions of separation were determined with the aid of central composite design.
The relationships between maximum tree height and building separation were determined.
The process conditions that provided the lowest starting times for glycerin separation were determined to be the reaction temperature of 50 °C, ultrasonication of 5 min and ultrasonication rate of 90%.
The residual concentrations of suspended sorbent particles in an aqueous medium through 5, 60, and 180 min of magnetic separation were determined by turbidimetry method.
To quantify the degree of similarity in grouping obtained by the 3 methods, both congruence between the typing methods and group separation were determined using Bionumerics software.
The binodal curve characterizing phase separation was determined.
Both experimental and simulation results show that the efficiency of separation is determined by a balance between pressure drop and droplet accumulation near the orifice.
The effect of polymer concentration and ethanol (EtOH) content in D2O/EtOH mixtures on the appearance and extent of the phase separation was determined.
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