Rotating-disk sorptive extraction: effect of the rotation mode of the extraction device on mass transfer efficiency
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2014Metadata
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Jachero, Lourdes
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Rotating-disk sorptive extraction: effect of the rotation mode of the extraction device on mass transfer efficiency
Abstract
The extraction device used in rotating-disk sorptive
extraction consists of a Teflon disk in which a sorptive phase
is fixed on one of its surfaces. Depending on the configuration,
the rotation axis of the disk device can be either perpendicular
or parallel to its radius, giving rise to two different
mass transfer patterns when rotating-disk sorptive extraction
is applied in liquid samples. In the perpendicular case
(configuration 1), which is the typical configuration, the disk
contains an embedded miniature stir bar that allows the disk
rotation to be driven using a common laboratory magnetic
stirrer. In the parallel case (configuration 2), the disk is driven
by a rotary rod connected to an electric stirrer. In this study,
triclosan and its degradation product methyl triclosan were
used as analyte models to demonstrate the significant effect of
the rotation configuration of the disk on the efficiency of
analyte mass transfer from water to a sorptive phase of
polydimethylsiloxane. Under the same experimental conditions
and at a rotation velocity of 1,250 rpm, extraction
equilibrium was reached at 80 min when the disk was
rotated in configuration 1 and at 30 min when the disk
was rotated in configuration 2. The extraction equilibration
time decreased to 14 min when the rotation velocity was
increased to 2,000 rpm in configuration 2. Because the
rotation pattern affects the mass transfer efficiency, each
rotation configuration was characterized through the
Reynolds number; Re values of 6,875 and 16,361 were
achieved with configurations 1 and 2, respectively, at
1,250 rpm.
General note
Artículo de publicación ISI
Patrocinador
The authors thank FONDECYT (projects 1100085
and 1110115), and L.J. thanks CONICYT for a doctoral award.
Quote Item
Anal Bioanal Chem (2014) 406:2987–2992
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