Individual metal recovery and separation by solvent extraction has
been an important technique
in pollution control as well as in hydrometallurgical processes.
Synergistic extraction and
separation of two cations, e.g., Cu(II) and Zn(II), a cation
and an anion, e.g., Cu(II) and Cr(VI),
and two cations and one anion, such as Cu(II), Zn(II), and
Cr(VI), have been demonstrated
employing a novel hydrophobic microporous hollow fiber membrane-based
(HFM) extraction
technique. The extraction selectivity of Cu(II) and
Zn(II) by LIX 84 (anti-2-hydroxy-5-nonylacetophenone oxime) and bis(2-ethylhexyl)phosphoric acid
(D2EHPA), respectively, in a
two-fiber-set HFM extractor is significantly enhanced due to
competitive extraction. The
efficiencies of extraction of Cu(II) and Cr(VI) by LIX 84 and
tri-n-octylamine (TOA), respectively,
are increased due to the self-control of the aqueous feed pH. A
simplified mathematical model
for synergistic extraction of Cu(II) and Zn(II) has been
developed. The model predicts the
observed extraction and separation performance well. In the novel
HFM extractor, the extraction
rates of Zn(II) and Cu(II) by D2EHPA and LIX 84,
respectively, were controlled by the aqueous
and organic boundary layer resistances as well as the interfacial
reaction resistances.
Many wastewaters as well as aqueous solutions used for
hydrometallurgical extractions have
multiple toxic heavy metals: some are present as cations; others are
present as anions. This
research is directed toward extracting multiple heavy metallic species
simultaneously into an
appropriate mixed solvent and then recovering and concentrating such
heavy metals into
appropriate aqueous stripping solutions. Heavy metals of interest
are Cu(II), Cr(VI), Zn(II),
Hg(II), etc. Such processes have been carried out in a
nondispersive fashion in microporous
hydrophobic hollow fiber membrane-based devices containing multiple
sets of fibers. The results
will be presented, and the basis of the observed synergism will be
discussed. The advantages
of such extraction-stripping processes will be pointed
out.
A solvent mixture of 1-hexanol and butyl acetate has been successfully used for the extraction of penicillin G. This solvent mixture may not only synergistically and effectively extract penicillin G, but also inhibit emulsion formation during the extraction of penicillin G from the filtrate of the fermentation broth. The equilibrium constants of the extraction, the molar ratios of 1-hexanol and penicillin G in the extracted species and the synergistic extraction of penicillin G have been studied by chemical analysis and by monitoring the absorbency shift in the FT-IR spectra of the functional groups in the solvents.
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