Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/23797
Title: Stripping of acetone from isopropanol solution with membrane and mesh gas-liquid contactors
Authors: Sun, Xiuyan 
Constantinou, Achilleas 
Gavriilidis, Asterios 
Major Field of Science: Natural Sciences
Field Category: Chemical Sciences
Keywords: Separations;Mass transfer;Microchannel;Model
Issue Date: Oct-2011
Source: Chemical Engineering and Processing: Process Intensification, 2011, vol. 50, no. 10, pp. 991-997
Volume: 50
Issue: 10
Start page: 991
End page: 997
Journal: Chemical Engineering and Processing: Process Intensification 
Abstract: Stripping of acetone from isopropanol utilizing nitrogen as a sweeping gas was conducted in gas/liquid contactors with slit type microchannels and containing flat sheet, metal and Teflon tortuous pore membranes or microfabricated metal meshes with straight pores. The contactor consisted of parallel metal plates, gaskets, and the membrane or the microstructured mesh so that passages for gas and liquid phases were formed. These slit type microchannels were 200 μm thick for both gas and liquid phases. All the membranes/meshes were wetted by the isopropanol solution. Breakthrough of one phase into the other was successfully described if contortion of the gas/liquid interface was considered at the pore ends. Various conditions during acetone stripping were investigated such as membrane type, gas and liquid flowrates and inlet acetone concentration. A contactor employing a Micro-Etch metal mesh with 76 μm openings and thickness of 50μm offered the lowest mass transfer resistance and resulted to the best acetone stripping performance. The separation efficiency increased by increasing the gas/liquid flowrate ratio, but was not affected when increasing the inlet acetone concentration. Good agreement between the experiments and an one-dimensional model with no adjustable parameters was observed.
URI: https://hdl.handle.net/20.500.14279/23797
ISSN: 02552701
DOI: 10.1016/j.cep.2011.06.004
Rights: © Elsevier B.V.
Type: Article
Affiliation : University College London 
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