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Aqueous biphasic systems (ABS) or aqueous two-phase systems (ATPS) are clean alternatives for traditional organic-water solvent extraction systems.. ABS are formed when either two polymers, one polymer and one kosmotropic salt, or two salts (one chaotropic salt and the other a kosmotropic salt) are mixed at appropriate concentrations or at a particular temperature.
This pregnant leach solution (PLS) is pumped to an extraction mixer settler where it is mixed with the organic phase (a kerosene hosted extractant). The copper transfers to the organic phase, and the aqueous phase (now called raffinate) is pumped back to the heap to recover more copper.
Phase 1 is typically an organic solvent and 2 an aqueous phase. Laboratory-scale liquid-liquid extraction. Photograph of a separatory funnel in a laboratory scale extraction of 2 immiscible liquids: liquids are a diethyl ether upper phase, and a lower aqueous phase. Schematic representation of a Soxhlet extractor:
The two liquids (typically an aqueous phase (heavy) and an organic phase (light)) enter the annular mixing zone where a liquid-liquid dispersion is formed and extraction occurs as solutes (e.g. dissolved metal ions) are transferred from one phase into the other. Inside the rotor, the liquids will be separated into a heavy (blue) and a light ...
Di(2-ethylhexyl)phosphoric acid (DEHPA or HDEHP) is an organophosphorus compound with the formula (C 8 H 17 O) 2 PO 2 H. The colorless liquid is a diester of phosphoric acid and 2-ethylhexanol . It is used in the solvent extraction of uranium , vanadium and the rare-earth metals .
The reaction is performed in a distillation apparatus so the formed alkene product can be distilled off and collected as the reaction proceeds. The water produced by the reaction as well as some acid will co-distill, giving a distillate mixture (2). The product is isolated from the mixture by the following work-up: [3]
To measure the partition coefficient of ionizable solutes, the pH of the aqueous phase is adjusted such that the predominant form of the compound in solution is the un-ionized, or its measurement at another pH of interest requires consideration of all species, un-ionized and ionized (see following).
With a typical liquid mass diffusivity in the order of 10 −9 m 2 /s, [2] the characteristic time for diffusion through a 20 micron thick liquid layer is 0.4 s. Therefore, the thinness of both phases (organic and aqueous) causes a relatively "immediate" mass transfer of guest species from one phase to the other, which means that this process has a low mass transfer resistance.